WO2014203688A1 - 粘着剤組成物およびそれを用いた粘着シート - Google Patents
粘着剤組成物およびそれを用いた粘着シート Download PDFInfo
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- WO2014203688A1 WO2014203688A1 PCT/JP2014/063885 JP2014063885W WO2014203688A1 WO 2014203688 A1 WO2014203688 A1 WO 2014203688A1 JP 2014063885 W JP2014063885 W JP 2014063885W WO 2014203688 A1 WO2014203688 A1 WO 2014203688A1
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- Prior art keywords
- pressure
- sensitive adhesive
- resin
- epoxy
- adhesive composition
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Classifications
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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
- C09J163/00—Adhesives based on epoxy resins; Adhesives based on derivatives of epoxy resins
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
- C08L33/08—Homopolymers or copolymers of acrylic acid esters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
-
- 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
- C09J133/08—Homopolymers or copolymers of acrylic acid esters
-
- 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
- C09J7/20—Adhesives in the form of films or foils characterised by their carriers
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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
- C09J2203/00—Applications of adhesives in processes or use of adhesives in the form of films or foils
- C09J2203/326—Applications of adhesives in processes or use of adhesives in the form of films or foils for bonding electronic components such as wafers, chips or semiconductors
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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
- C09J2433/00—Presence of (meth)acrylic polymer
-
- 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
- C09J2463/00—Presence of epoxy resin
Definitions
- the present invention relates to a pressure-sensitive adhesive composition, and more specifically, it can be easily re-applied, does not cause floating or peeling, and does not cause adhesive residue even when peeled after being placed in a high-temperature environment.
- the present invention relates to an adhesive composition and an adhesive film using the same.
- Electronic boards and wiring boards used in various electronic devices are manufactured through various processes such as mounting of electronic components on the board, lead frame fabrication, soldering, and heat treatment.
- a protective film that can be peeled off from the surface of the board to protect the mounted electrical components or prevent paint or solder from adhering to locations other than the desired location during lead frame processing or soldering.
- the protective film is peeled off after work.
- Such a protective film has a layer structure in which a pressure-sensitive adhesive layer is provided on one surface of a film substrate, and the protective film is bonded to an electronic substrate or the like that is an adherend. Bonded to the adherend.
- the protective film as described above needs to be in close contact with the substrate without being lifted or peeled off in each step of manufacturing an electronic substrate or a wiring substrate.
- a protective film with high adhesive strength so that it does not float or peel some electronic substrates have extremely thin ones, and when peeling the protective film from such an electronic substrate with low self-supporting property, There is a problem that the electronic substrate itself is damaged.
- Japanese Patent Application Laid-Open No. 2008-1992917 uses a free epoxy group-containing compound instead of an epoxy curing agent added to an acrylic pressure-sensitive adhesive. Proposed.
- an epoxy resin, a curing agent for epoxy resin, and a glass transition temperature of 60 ° C. or higher are used as a dicing tape capable of improving the bonding reliability between a semiconductor chip and an adherend. It has been proposed to use, as an adhesive, a curable composition containing two epoxy group-containing acrylic resins having different molecular weights.
- JP 2012-70112 discloses graft polymerization of a chain containing a cyclic ether group-containing monomer as an acrylic adhesive as a heat-resistant adhesive that hardly causes adhesive residue ( It has been proposed to use a product obtained by adding a curing agent to a (meth) acrylic polymer.
- 2013-040323 discloses that a protective sheet having both adhesiveness and adhesive residue has a gel fraction of 60% or more and an alkyl ester having 6 or more carbon atoms as an adhesive. It has been proposed to use an acrylic polymer consisting of a monomer having the same.
- the pressure-sensitive adhesive described in Japanese Patent Application Laid-Open No. 2008-192917 is excellent in releasability, it contains an epoxy group-containing compound as a free component in the pressure-sensitive adhesive. In some cases, the compound remained and contaminated the substrate as the adherend.
- the adhesive described in International Publication WO2011 / 115159 pamphlet uses an epoxy resin having an epoxy group having a glass transition temperature of 60 ° C. or higher, so that the cohesive force is large.
- the acrylic resin having a group is difficult to peel off after being bonded to an adherend because the curing reaction proceeds and the adhesiveness is developed in a high temperature environment such as heat treatment.
- the pressure-sensitive adhesive described in Japanese Patent Application Laid-Open No. 2012-70112 does not increase the adhesive force even when the pressure-sensitive adhesive is placed in a high-temperature environment such as heat treatment. Although contamination (residue residue) can be reduced, it is difficult to adjust the adhesion with the adherend because the chain containing the cyclic ether group-containing monomer is graft-polymerized (meth) acrylic polymer, Depending on the type of adherend to which the masking tape (adhesive sheet) is bonded, there may be cases where floating or peeling occurs.
- the pressure-sensitive adhesive described in JP2013-040323A does not contain a component having a higher cohesive force than the acrylic resin (high glass transition temperature component), so that the pressure-sensitive adhesive force in a high-temperature environment is insufficient. There was a case.
- the inventors of the present invention have recently achieved the initial adhesive strength by using, as an adhesive, a resin obtained by adding a predetermined amount of an epoxy thermosetting resin and a curing agent to an acrylic resin and curing the epoxy thermosetting resin. Low, so it can be easily reattached even if it is a thin film-like adherend that does not have self-supporting properties, and it does not float or peel off after being attached to the adherend. Even when placed underneath, the adhesive strength did not change and it had excellent peelability, so that it was possible to reduce the contamination of the adherend due to adhesive residue and the like.
- thermosetting epoxy resin as an epoxy resin, and not only in the heating process, but also in the chemical treatment process, it can suppress floating and peeling after bonding to the adherend. I got the knowledge.
- the present invention is based on this finding.
- the object of the present invention is that the initial adhesive force is low, so that even a thin film-like adherend having no self-supporting property can be easily reattached. Even if it is treated, it does not float or peel off, and even when it is placed in a high temperature environment, it has excellent peelability without changing the adhesive force. It is an object to provide a pressure-sensitive adhesive composition that can reduce contamination of a body and a pressure-sensitive adhesive sheet using the same.
- the pressure-sensitive adhesive composition according to the present invention is a pressure-sensitive adhesive composition comprising an acrylic resin, an epoxy thermosetting resin, and a curing agent for curing the epoxy thermosetting resin,
- the epoxy thermosetting resin is contained in the range of 20% by mass to 60% by mass with respect to the acrylic resin.
- the epoxy thermosetting resin has an epoxy equivalent of 100 g / eq. Or more, 2000 g / eq. The following is preferable.
- the epoxy thermosetting resin preferably has a mass average molecular weight of 300 or more and 5000 or less.
- the acrylic resin preferably has a mass average molecular weight of 100,000 or more and 2 million or less.
- the pressure-sensitive adhesive sheet according to another embodiment of the present invention is a pressure-sensitive adhesive sheet comprising a base material and a pressure-sensitive adhesive layer provided on one surface side of the base material, wherein the pressure-sensitive adhesive layer is an acrylic sheet.
- the pressure-sensitive adhesive layer is an acrylic sheet.
- Comprising a resin and an epoxy thermosetting resin The epoxy thermosetting resin is contained in the range of 20% by mass to 60% by mass with respect to the acrylic resin.
- a release sheet is provided on the side of the pressure-sensitive adhesive layer opposite to the substrate side.
- a method for producing a pressure-sensitive adhesive sheet according to another embodiment of the present invention is a method for producing a pressure-sensitive adhesive sheet comprising a base material and a pressure-sensitive adhesive layer provided on one surface side of the base material, Apply the adhesive composition on one side of the substrate, Forming a pressure-sensitive adhesive layer by heating and curing the pressure-sensitive adhesive composition;
- the pressure-sensitive adhesive composition comprises an acrylic resin, an epoxy thermosetting resin, and a curing agent for curing the epoxy thermosetting resin,
- the epoxy thermosetting resin is contained in the range of 20% by mass to 60% by mass with respect to the acrylic resin.
- the pressure-sensitive adhesive composition is applied to one side of the substrate and dried, A release sheet is provided on the surface of the pressure-sensitive adhesive composition to form a laminate,
- the pressure-sensitive adhesive layer is formed by heating the laminate and curing the pressure-sensitive adhesive composition. It is preferable to comprise.
- the initial adhesive force is low by using, as an adhesive, a resin obtained by adding a predetermined amount of an epoxy thermosetting resin and a curing agent to the acrylic resin and curing the epoxy thermosetting resin. Therefore, even thin film adherends that are not self-supporting can be easily reattached, and after bonding to the adherend, there is no lifting or peeling, and in a high temperature environment. Even when it is placed, the adhesive force does not change and has excellent releasability, so that contamination of the adherend due to adhesive residue and the like can be reduced.
- the pressure-sensitive adhesive composition according to the present invention is excellent in chemical resistance because it contains an epoxy thermosetting resin.
- the pressure-sensitive adhesive composition according to the present invention does not contain a silicone pressure-sensitive adhesive and is silicone-free, it can be used as a pressure-sensitive adhesive sheet (masking sheet) for various electronic devices.
- the pressure-sensitive adhesive composition according to the present invention contains an acrylic resin, an epoxy thermosetting resin, and a curing agent as essential components.
- an acrylic resin an epoxy thermosetting resin
- a curing agent as essential components.
- the acrylic resin which comprises the adhesive composition by this invention can use suitably the acrylic resin which has (meth) acrylic acid ester as a main component.
- (meth) acrylic acid shall mean acrylic acid and / or methacrylic acid.
- (meth) acrylic acid esters examples include methyl ester, ethyl ester, propyl ester, isopropyl ester, butyl ester, isobutyl ester, s-butyl ester, t-butyl ester, pentyl ester, isopentyl ester, hexyl ester, heptyl ester, Octyl ester, 2-ethylhexyl ester, isooctyl ester, nonyl ester, isononyl ester, decyl ester, isodecyl ester, undecyl ester, dodecyl ester, tridecyl ester, tetradecyl ester, hexadecyl ester, octadecyl ester, eicosyl (Meth) acrylic acid alkyl esters such as esters having 1 to 30 carbon atoms, particularly linear or branched alkyl esters
- the functional group-containing (meth) acrylate copolymerizable with the above (meth) acrylic acid ester acrylic acid, methacrylic acid, carboxyethyl (meth) acrylate, carboxypentyl (meth) acrylate, itaconic acid, maleic acid , Carboxyl group-containing monomers such as fumaric acid and crotonic acid, acid anhydride group-containing monomers such as maleic anhydride and itaconic anhydride, 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, ( 4-hydroxybutyl (meth) acrylate, 6-hydroxyhexyl (meth) acrylate, 8-hydroxyoctyl (meth) acrylate, 10-hydroxydecyl (meth) acrylate, 12-hydroxylauryl (meth) acrylate, ( 4-hydroxymethylcyclohexyl) me Hydroxyl group-containing monomers such as ru (meth)
- monomers containing nitrogen atoms such as cyano group-containing monomers such as acrylonitrile, amide group-containing monomers such as acrylamide, amino group-containing monomers such as N, N-dimethylaminoethyl (meth) acrylate, and isocyanate group-containing monomers may be used. It may be used as a polymerization component.
- the acrylic resin (copolymer) used in the present invention can be obtained by polymerizing the above monomers by a method such as ordinary solution polymerization, bulk polymerization, emulsion polymerization or suspension polymerization.
- the acrylic resin is preferably produced by solution polymerization obtained as a solution. By obtaining the acrylic resin as a solution, it can be used as it is for producing the pressure-sensitive adhesive composition of the present invention.
- Examples of the solvent used for the solution polymerization include organic solvents such as ethyl acetate, toluene, n-hexane, acetone, and methyl ethyl ketone.
- Examples of the polymerization initiator used in the polymerization include peroxides such as benzoyl peroxide and lauryl peroxide, azobis compounds such as azobisisobutyronitrile and azobisvaleronitrile, and polymer azo polymerization initiators. These can be used alone or in combination.
- polymerization in order to adjust the molecular weight of an acrylic resin, a conventionally well-known chain transfer agent can be used.
- the mass average molecular weight of the acrylic copolymer described above is preferably in the range of 100,000 to 2 million, more preferably in the range of 200,000 to 1 million. If the weight average molecular weight is less than 100,000, the pressure-sensitive adhesive composition may be inferior in tackiness. On the other hand, if the weight average molecular weight exceeds 2,000,000, the coating property of the pressure-sensitive adhesive composition may be deteriorated. In some cases, the compatibility with the thermosetting resin is lowered, making it difficult to obtain desired tackiness.
- the mass average molecular weight can be measured by GPC (gel permeation chromatography) using a polystyrene standard sample.
- the epoxy thermosetting resin used in the pressure-sensitive adhesive composition according to the present invention is a prepolymer having at least one epoxy group or glycidyl group, and can be cured by a crosslinking polymerization reaction in combination with a curing agent. If there is, it can be used without any particular limitation.
- a thermosetting epoxy resin By using such a thermosetting epoxy resin, the chemical resistance of the pressure-sensitive adhesive composition can be improved. As a result, even if chemical treatment is performed after bonding to the adherend, The occurrence of peeling can be suppressed.
- an epoxy thermosetting resin means the precursor or composition before resin hardens
- Epoxy equivalent is 100 g / eq. If the epoxy thermosetting resin is less than 1, the cross-linking density becomes too high, and the tackiness may decrease from the desired range, while 2000 g / eq. In the case of an epoxy thermosetting resin exceeding 1, when the pressure-sensitive adhesive composition is cured to form a pressure-sensitive adhesive layer, the heat resistance of the pressure-sensitive adhesive layer may be insufficient.
- an epoxy equivalent is the gram number of resin containing the epoxy group of 1 gram equivalent measured by the method based on JISK7236.
- epoxy thermosetting resins include bisphenol type epoxy resins such as bisphenol A type epoxy resins and bisphenol F type epoxy resins, novolac type epoxy resins such as novolac epoxy resins and cresol novolac epoxy resins, biphenyl type epoxy resins, and stilbene.
- Type epoxy resin triphenolmethane type epoxy resin, alkyl-modified triphenolmethane type epoxy resin, triazine nucleus-containing epoxy resin, dicyclopentadiene-modified phenol type epoxy resin, etc., phenol novolac resin, cresol novolak Resin, novolac phenol resin such as bisphenol A novolac resin, phenol resin such as resol phenol resin, urea (urea) resin, melamine resin, etc.
- Resins having an azine ring unsaturated polyester resins, bismaleimide resins, polyurethane resins, diallyl phthalate resins, alkoxy group-containing silane-modified epoxy resins, resins having a benzoxazine ring, cyanate ester resins.
- an epoxy resin having a rigid structure such as a biphenyl skeleton, a bisphenol skeleton, or a stilbene skeleton in the main chain is preferable, more preferably a bisphenol type epoxy resin, and particularly preferably a bisphenol A type epoxy. Resin.
- the above-mentioned bisphenol A type epoxy resin may be liquid at room temperature or solid at room temperature depending on the number of repeating units of the bisphenol skeleton.
- the bisphenol A type epoxy resin having 1 to 3 carbon atoms in the main chain is liquid at normal temperature
- the bisphenol A type epoxy resin having 2 to 10 carbon atoms in the main chain is solid at normal temperature.
- Such a relatively low molecular weight bisphenol A type epoxy resin has crystallinity, and even if it is a solid substance that is crystallized at room temperature, it rapidly melts and changes to a low viscosity liquid. .
- Such a relatively low molecular weight bisphenol A type epoxy resin is characterized by high curability and low hygroscopicity (because the free volume is small) because the crosslink density is high upon curing.
- the bisphenol A type epoxy resin solid at normal temperature those having a glass transition temperature in the range of 50 ° C. or higher and 150 ° C. or lower are preferable from the viewpoint of mechanical strength and heat resistance.
- JER828 manufactured by Japan Epoxy Resin Co., Ltd. is a bisphenol A type epoxy having a main chain of 2 to 10 which is solid at normal temperature.
- Examples of the resin include JER1001 manufactured by Japan Epoxy Resin Co., Ltd.
- the above-described epoxy thermosetting resin needs to be contained in the range of 20% by mass to 60% by mass with respect to the acrylic resin.
- an adhesive composition having a low initial adhesive force and capable of maintaining the adhesive force even when placed in a high temperature environment, and having little adhesive residue. It can be a thing.
- the amount of the epoxy thermosetting resin is less than 20% by mass, the initial adhesive force tends to increase, and when the adhesive is placed in a high temperature environment, the adhesive force tends to increase.
- the epoxy thermosetting resin is added in an amount exceeding 60% by mass, the initial adhesive strength (tack) is lowered, and it may be difficult to bond the adhesive sheet to the adherend at room temperature.
- a preferable content of the epoxy thermosetting resin is in a range of 30% by mass to 50% by mass with respect to the acrylic resin.
- ⁇ Curing agent> The epoxy thermosetting resin described above is cured by heating and the like, but in the present invention, a curing agent for promoting the curing reaction is included in the pressure-sensitive adhesive composition.
- a curing agent that reacts with an epoxy resin in an equivalent amount for example, an amine-based curing agent, an acid anhydride-based curing agent, and a phenol-based curing agent can be suitably used, and an epoxy resin can be used alone.
- an epoxy resin can be used alone.
- a curing agent that can be cured (polymerized) with imidazole for example, an imidazole curing agent or a cationic curing agent can be preferably used.
- amine curing agents examples include aliphatic polyamines such as diethylenetriamine (DETA), triethylenetetramine (TETA), and metaxylylenediamine (MXDA), diaminodiphenylmethane (DDM), m-phenylenediamine (MPDA), and diaminodiphenylsulfone.
- DETA diethylenetriamine
- TETA triethylenetetramine
- MXDA metaxylylenediamine
- DDM diaminodiphenylmethane
- MPDA m-phenylenediamine
- diaminodiphenylsulfone examples include aliphatic polyamines such as diethylenetriamine (DETA), triethylenetetramine (TETA), and metaxylylenediamine (MXDA), diaminodiphenylmethane (DDM), m-phenylenediamine (MPDA), and diaminodiphenylsulfone.
- DDS di
- the acid anhydride curing agent examples include alicyclic acid anhydrides (liquid acid anhydrides) such as hexahydrophthalic anhydride (HHPA) and methyltetrahydrophthalic anhydride (MTHPA), trimellitic anhydride (TMA), And aromatic acid anhydrides such as pyromellitic anhydride (PMDA) and benzophenone tetracarboxylic acid (BTDA).
- alicyclic acid anhydrides liquid acid anhydrides
- HHPA hexahydrophthalic anhydride
- MTHPA methyltetrahydrophthalic anhydride
- trimellitic anhydride TMA
- aromatic acid anhydrides such as pyromellitic anhydride (PMDA) and benzophenone tetracarboxylic acid (BTDA).
- phenolic curing agent examples include phenol novolac resin, bisphenol novolac resin, poly p-vinylphenol, and the like. The aforementioned curing agents may be used
- imidazole curing agents include imidazole, 2-methylimidazole, 2-ethylimidazole, 2-ethyl-4-methylimidazole, 2-isopropylimidazole, 2-phenylimidazole, carboxylic acid salts of imidazole compounds, and epoxy compounds. And adducts.
- cationic curing agents include sulfonic acid esters, imide sulfonates, dialkyl-4-hydroxysulfonium salts, arylsulfonic acid-p-nitrobenzyl esters, silanol-aluminum complexes, aromatic iodonium salts, aromatic sulfonium salts, aromatic diazonium. And salts, aromatic phosphonium salts, triazine compounds, iron arene complexes, and the like.
- the aforementioned curing agents may be used alone or in combination of two or more.
- the blending amount of the above-mentioned crosslinking agent is not particularly limited, but if the blending amount with respect to the epoxy thermosetting resin is small, the epoxy composition is cured when the pressure-sensitive adhesive composition is cured to form the pressure-sensitive adhesive layer. Insufficient curing such as an increase in the curing time of the thermosetting resin tends to be difficult, and it tends to be difficult to obtain desired tackiness. On the other hand, when the compounding amount of the curing agent is excessive, the storage stability of the pressure-sensitive adhesive composition may be reduced, or the curing density of the epoxy thermosetting resin may become too high to obtain desired tackiness.
- the curing agent when using a curing agent capable of curing (polymerizing) an epoxy resin alone, the curing agent may be blended within a range of 1% by mass to 20% by mass with respect to the epoxy thermosetting resin. Moreover, what is necessary is just to mix
- the pressure-sensitive adhesive composition according to the present invention may contain a crosslinking agent.
- a crosslinking agent By adding a crosslinking agent, stickiness can be improved while maintaining the adhesive strength.
- a conventionally well-known thing can be used as a crosslinking agent, For example, a polyfunctional epoxy compound and an isocyanate compound are mentioned.
- Polyfunctional epoxy compounds include sorbitol polyglycidyl ether, polyglycerol polyglycidyl ether, pentaerythritol polyglycidyl ether, diglycerol polyglycidyl ether, glycerol polyglycidyl ether, trimethylolpropane polyglycidyl ether, neopentyl glycol diglycidyl ether, 1 , 6-hexanediol diglycidyl ether, hydrogenated bisphenol A diglycidyl ether, polyethylene glycol diglycidyl ether, polypropylene glycol diglycidyl ether, polybutadiene diglycidyl ether, and the like.
- the isocyanate compound a polyisocyanate compound, a trimer of a polyisocyanate compound, a urethane prepolymer having an isocyanate group at a terminal obtained by reacting a polyisocyanate compound and a polyol compound, a trimer of the urethane prepolymer Etc.
- polyisocyanate compound examples include 2,4-tolylene diisocyanate, 2,5-tolylene diisocyanate, 1,3-xylylene diisocyanate, 1,4-xylylene diisocyanate, diphenylmethane-4,4′-diisocyanate, 3 -Methyldiphenylmethane diisocyanate, hexamethylene diisocyanate, isophorone diisocyanate, dicyclohexylmethane-4,4'-diisocyanate, dicyclohexylmethane-2,4'-diisocyanate, lysine isocyanate and the like.
- crosslinking agents may be used alone or in combination of two or more.
- the pressure-sensitive adhesive composition according to the present invention can be applied to, for example, processability, heat resistance, weather resistance, mechanical properties, dimensional stability, antioxidant properties, slipperiness, releasability, and flame retardancy as necessary.
- processability heat resistance, weather resistance, mechanical properties, dimensional stability, antioxidant properties, slipperiness, releasability, and flame retardancy as necessary.
- lubricants plasticizers, fillers, fillers, antistatic agents, antiblocking agents, crosslinking agents, light stabilizers, dyes
- a colorant such as a pigment, and the like may be added.
- a coupling agent such as silane, titanium, and aluminum can be further included.
- the pressure-sensitive adhesive composition according to the present invention can be prepared by mixing the above-described components and kneading and dispersing as necessary.
- the mixing or dispersing method is not particularly limited, and a conventional kneading and dispersing machine such as a two-roll mill, a three-roll mill, a pebble mill, a tron mill, a Szegvari attritor, a high-speed impeller disperser, a high-speed stone mill, A high speed impact mill, a desper, a high speed mixer, a ribbon blender, a kneader, an intensive mixer, a tumbler, a blender, a desperser, a homogenizer, an ultrasonic disperser, and the like can be applied.
- a diluent solvent may be added to mix each component.
- the pressure-sensitive adhesive sheet according to the present invention comprises a base material and a pressure-sensitive adhesive layer provided on one surface side of the base material, and the pressure-sensitive adhesive layer is obtained by thermosetting the above-mentioned pressure-sensitive adhesive composition. It is what you use.
- the base material various forms such as a film, a sheet, or a tape can be used according to the intended use.
- the material for the substrate can be appropriately selected depending on the intended use, and is not particularly limited.
- low density polyethylene linear low density polyethylene, high density polyethylene, ethylene-propylene copolymer, polypropylene, polybutene, polybutadiene, polymethylpentene, ethylene-vinyl acetate copolymer
- Polyolefin resins such as polyethylene terephthalate and polyethylene naphthalate, polyamide resins such as nylon 6,6 and nylon 1,12, polyimide, ethylene- (meth) acrylic acid copolymer, ethylene- (meth) acrylic Acrylic copolymer such as methyl acid copolymer, ethylene-ethyl (meth) acrylate copolymer, etc.
- polyvinyl chloride resin vinyl chloride vinyl acetate copolymer, ethylene-vinyl chloride
- the base material composed of polyimide resin, polyphenylene sulfide resin, polyester resin has heat resistance, strength and flexibility, dimensional stability, energy ray permeability, stiffness, extensibility, Since it is excellent in lamination suitability and chemical resistance, it is preferably used as a base material for temporarily fixing or protecting the electronic component in the manufacturing process of the electronic component.
- These resins can be made into various forms such as film, sheet, or tape by forming into a sheet or film by extrusion molding and processing into a predetermined shape. Alternatively, two or more kinds of resins may be used in combination.
- the sheet or film formed by extrusion molding may be uniaxially stretched or biaxially stretched from the viewpoint of mechanical strength, or may be a laminated structure of two or more layers by a technique such as coextrusion. .
- the thickness of the base material is not particularly limited, and when the adhesive sheet is used as a protective sheet for an electronic circuit board or the like, it may be a thickness required according to the application, for example, 5 ⁇ m or more and 500 ⁇ m or less. Can be used.
- the base material may be subjected to corona treatment or primer treatment on the surface side of the base material on which the pressure-sensitive adhesive composition is applied in order to enhance the adhesion with the pressure-sensitive adhesive layer.
- the pressure-sensitive adhesive sheet according to the present invention can be obtained by forming the pressure-sensitive adhesive layer by applying the above-mentioned pressure-sensitive adhesive composition to one side of the substrate and heating and curing the pressure-sensitive adhesive composition.
- the method for applying the pressure-sensitive adhesive composition to the substrate is not particularly limited. For example, roll coating, reverse roll coating, transfer roll coating, gravure coating, gravure reverse coating, comma coating, rod coating, blade coating Bar coat, wire bar coat, die coat, lip coat, dip coat, etc. can be applied.
- the pressure-sensitive adhesive composition is cured by heating to form a pressure-sensitive adhesive layer.
- the heating temperature at the time of curing is about 50 to 150 ° C., preferably 90 to 120 ° C.
- the heating time may be appropriately adjusted depending on the heating temperature, but when the heating temperature is 90 ° C. or higher and 150 ° C. or lower, it is 1 to 240 minutes, preferably several minutes to 60 minutes.
- the heating temperature is 50 ° C. or more and 90 ° C. or less, it is 1 day (24 hours) to 7 days (168 hours), preferably 2 days (48 hours) to 5 days (120 hours).
- cohesive force improves by hardening an adhesive layer beforehand before using an adhesive sheet, and the heat resistance and chemical resistance of an adhesive sheet improve.
- a release sheet may be provided on the surface of the pressure-sensitive adhesive layer opposite to the base material side in consideration of its handleability.
- the adhesive composition is applied to one side of the substrate and dried, and the release sheet is applied to the surface of the adhesive composition (the side opposite to the side with the substrate). After being provided, the pressure-sensitive adhesive composition may be thermally cured to form a pressure-sensitive adhesive layer.
- the release sheet conventionally known ones such as a release film, a separate paper, a separate film, a separate paper, a release film, and a release paper can be suitably used. Moreover, you may use what formed the release layer in the single side
- the release layer is not particularly limited as long as it has a releasability, and examples thereof include silicone resins, organic resin-modified silicone resins, fluororesins, aminoalkyd resins, melamine resins, acrylic resins, and polyester resins. It is done. These resins can be used in any of emulsion type, solvent type and solventless type.
- the release sheet is formed by applying a coating liquid in which a release layer component is dispersed and / or dissolved to one side of a release paper base film, followed by heating and drying and / or curing.
- a coating method of the coating liquid a known and arbitrary coating method can be applied, for example, roll coating, gravure coating, spray coating and the like.
- the pressure-sensitive adhesive sheet having a release sheet is attached by peeling the release sheet from the pressure-sensitive adhesive sheet and bonding the release surface of the pressure-sensitive adhesive sheet to the adherend before bonding the pressure-sensitive adhesive sheet to the adherend.
- An adhesive sheet can be applied to the surface of the body. Therefore, the pressure-sensitive adhesive sheet according to the present invention can be used as a masking sheet for an electronic circuit board, etc., and can be easily reapplied even if the circuit board is extremely thin. After joining, there is no floating or peeling, and even when placed in a high temperature environment, the adhesive strength does not change and it has excellent peelability, so circuit boards etc. due to adhesive residue etc. Contamination can also be reduced. Moreover, even if a chemical treatment or the like is performed after bonding to the adherend, the occurrence of floating or peeling can be suppressed.
- Example 1 Preparation of pressure-sensitive adhesive composition> Acrylic copolymer resin (mass average molecular weight of 20) containing, as monomer units, methyl acrylate, 2-ethylhexyl acrylate, acrylic acid, and 2-hydroxyethyl acrylate in a mass ratio of 50: 40: 0.5: 9.5, respectively. And a glass transition temperature of 6 ° C.).
- the obtained pressure-sensitive adhesive composition was subjected to an easy release treatment of a 38 ⁇ m thick polyester film (trade name: SP-PET-01, manufactured by Mitsui Chemicals, Inc.) on which one side was subjected to an easy release treatment using a silicone release agent. After coating the entire surface using an applicator, it was dried in a drying oven at 110 ° C. for 1 minute to form an adhesive layer having a thickness of 10 ⁇ m.
- a pressure-sensitive adhesive sheet 1 was obtained by laminating a polyimide film substrate (trade name: Kapton 100H, manufactured by Toray DuPont) with a thickness of 25 ⁇ m on the surface of the formed pressure-sensitive adhesive layer and curing at 60 ° C. for 120 hours.
- Example 3 Instead of the liquid epoxy resin used in Example 1, a solid epoxy resin (bisphenol A type epoxy resin, epoxy equivalent: 480 g / eq., Molecular weight: 900, trade name: jER1001, manufactured by Mitsubishi Chemical Corporation) was used, and an epoxy was used. Except having changed the compounding quantity of resin and a hardening
- bisphenol A type epoxy resin epoxy equivalent: 480 g / eq., Molecular weight: 900, trade name: jER1001, manufactured by Mitsubishi Chemical Corporation
- Example 4 A pressure-sensitive adhesive sheet 4 was obtained in the same manner as in Example 3 except that the blending amounts of the solid epoxy resin and the curing agent were changed according to Table 1 below.
- Example 5 In place of the liquid epoxy resin used in Example 1, an alkoxy group-containing silane-modified epoxy resin (solid content 57% by mass, epoxy equivalent: 1420 g / eq., Molecular weight: 2400, trade name: Composelan E103D, manufactured by Arakawa Chemical Industries) was used, and the pressure-sensitive adhesive sheet 5 was obtained in the same manner as in Example 1 except that the blending amounts of the epoxy resin and the curing agent were changed according to Table 1.
- an alkoxy group-containing silane-modified epoxy resin solid content 57% by mass, epoxy equivalent: 1420 g / eq., Molecular weight: 2400, trade name: Composelan E103D, manufactured by Arakawa Chemical Industries
- Example 6 Except having changed the compounding quantity of an epoxy resin and a hardening
- Example 7 In Example 4, Example 4 was added except that 0.2 parts by mass of an epoxy crosslinking agent (solid content: 50% by mass, trade name: E-5C, manufactured by Soken Chemical Co., Ltd.) was added as a crosslinking agent to the adhesive composition. In the same manner as above, an adhesive sheet 7 was obtained.
- an epoxy crosslinking agent solid content: 50% by mass, trade name: E-5C, manufactured by Soken Chemical Co., Ltd.
- Example 8 In place of the polyimide film substrate having a thickness of 25 ⁇ m used in Example 4, a polyester film substrate having a thickness of 50 ⁇ m (trade name: A4100, manufactured by Toyobo Co., Ltd.) was used. Sheet 8 was obtained.
- Example 9 A portion of the solid epoxy resin used in Example 8 was added to an alkoxy group-containing silane-modified epoxy resin (solid content 57% by mass, epoxy equivalent: 1420 g / eq., Molecular weight: 2400, trade name: The adhesive was changed in the same manner as in Example 8 except that the composition was changed to Composelan E103D (Arakawa Chemical Industries, Ltd.) and the curing agent was changed to 1-benzyl-2-methylimidazole (trade name: Casol 1B2MZ, Shikoku Kasei Co., Ltd.). Sheet 9 was obtained.
- Composelan E103D Arakawa Chemical Industries, Ltd.
- 1-benzyl-2-methylimidazole trade name: Casol 1B2MZ, Shikoku Kasei Co., Ltd.
- Example 10 A portion of the solid epoxy resin used in Example 8 was added to an alkoxy group-containing silane-modified epoxy resin (solid content 57% by mass, epoxy equivalent: 1420 g / eq., Molecular weight: 2400, trade name:
- the adhesive was changed in the same manner as in Example 8 except that the composition was changed to Composelan E103D (Arakawa Chemical Industries, Ltd.) and the curing agent was changed to 1-benzyl-2-methylimidazole (trade name: Casol 1B2MZ, Shikoku Kasei Co., Ltd.). Sheet 10 was obtained.
- Example 11 Part of the solid epoxy resin used in Example 8 was a liquid epoxy resin (polycondensate of bisphenol A / epichlorohydrin / dimer acid, epoxy equivalent: 600 to 700 g / eq., Trade name: adhesive sheet 11 in the same manner as in Example 8 except that the curing agent was changed to 1-benzyl-2-methylimidazole (trade name: Cyasol 1B2MZ, manufactured by Shikoku Kasei Co., Ltd.). Got.
- a liquid epoxy resin polycondensate of bisphenol A / epichlorohydrin / dimer acid, epoxy equivalent: 600 to 700 g / eq.
- Trade name adhesive sheet 11 in the same manner as in Example 8 except that the curing agent was changed to 1-benzyl-2-methylimidazole (trade name: Cyasol 1B2MZ, manufactured by Shikoku Kasei Co., Ltd.).
- Comparative Example 1 A pressure-sensitive adhesive sheet 12 was obtained in the same manner as in Example 3 except that the blending amounts of the solid epoxy resin and the curing agent were changed according to Table 2 below.
- Comparative Example 3 A pressure-sensitive adhesive sheet 14 was obtained in the same manner as in Example 5 except that the blending amounts of the epoxy resin and the curing agent were changed according to Table 2 below.
- Comparative Example 4 100 parts by mass of an acrylic pressure-sensitive adhesive (trade name: SK1439U, manufactured by Soken Chemical Co., Ltd.) and 0.6 mass of an epoxy crosslinking agent (solid content: 50% by mass, product name: E-5C, manufactured by Soken Chemical Co., Ltd.) as a curing agent Are dissolved in 151.5 parts by mass of a mixed solvent of toluene and methyl ethyl ketone (trade name: KT-11, mass ratio 1: 1, manufactured by DIC Graphics) and stirred with a disper at a rotation speed of 500 rpm for 30 minutes.
- the pressure-sensitive adhesive composition was obtained by allowing to stand until air bubbles disappeared at room temperature.
- the obtained pressure-sensitive adhesive composition was subjected to an easy release treatment of a 38 ⁇ m thick polyester film (trade name: SP-PET-01, manufactured by Mitsui Chemicals, Inc.) on which one side was subjected to an easy release treatment using a silicone release agent. After coating the entire surface using an applicator, it was dried in a drying oven at 100 ° C. for 2 minutes to form an adhesive layer having a thickness of 10 ⁇ m.
- a pressure-sensitive adhesive sheet 15 was obtained by laminating a polyimide film substrate (trade name: Kapton 100H, manufactured by Toray DuPont) having a thickness of 25 ⁇ m on the surface of the formed pressure-sensitive adhesive layer.
- Comparative Example 5 100 parts by mass of an acrylic pressure-sensitive adhesive (trade name: SK1439U, manufactured by Soken Chemical Co., Ltd.) and 0.6 mass of an epoxy crosslinking agent (solid content: 50% by mass, product name: E-5C, manufactured by Soken Chemical Co., Ltd.) as a curing agent And 6 parts by mass of a solid epoxy resin (bisphenol A type epoxy resin, trade name: jER1001, manufactured by Mitsubishi Chemical Corporation), a mixed solvent of toluene and methyl ethyl ketone (trade name: KT-11, mass ratio 1: 1) The product was dissolved in 157.5 parts by mass of DIC Graphics Co., Ltd., stirred with a disper at 500 rpm for 30 minutes, and then allowed to stand at room temperature until there were no air bubbles to obtain an adhesive composition. A pressure-sensitive adhesive sheet 16 was obtained in the same manner as in Comparative Example 4 using the obtained pressure-sensitive adhesive composition.
- an acrylic pressure-sensitive adhesive trade name: SK1439U, manufactured by Soken
- Comparative Example 6 Preparation of pressure-sensitive adhesive composition> 100 parts by weight of a silicone adhesive having a solid content of 60% by mass (trade name: SD4600, manufactured by Toray Dow Corning) and two curing catalysts (trade names: SRX212 and BY24-741, both of which are Toray Dow Corning) 0.9 parts by weight and 1.5 parts by weight, respectively, were dissolved in 100 parts by weight of a mixed solvent of toluene and methyl ethyl ketone (trade name: KT-11, weight ratio 1: 1, manufactured by DIC Graphics). The mixture was stirred with a disper at 500 rpm for 30 minutes, and then allowed to stand at room temperature until there were no bubbles, thereby obtaining a pressure-sensitive adhesive composition.
- a silicone adhesive having a solid content of 60% by mass trade name: SD4600, manufactured by Toray Dow Corning
- two curing catalysts trade names: SRX212 and BY24-741, both of which are Toray Dow Corning
- the obtained pressure-sensitive adhesive composition was coated on the entire surface of a polyimide film substrate (trade name: Kapton 100H, manufactured by Toray DuPont) with a thickness of 25 ⁇ m using an applicator, and then dried at 100 ° C. in a drying oven. It was dried for 2 minutes to form an adhesive layer having a thickness of 10 ⁇ m.
- a pressure-sensitive adhesive sheet 17 was obtained by laminating a polypropylene film (trade name: Treffan BO-2500 # 40) having a thickness of 40 ⁇ m on the surface of the formed pressure-sensitive adhesive layer.
- Comparative Example 7 In place of the polyimide film substrate having a thickness of 25 ⁇ m used in Comparative Example 4, a polyester film substrate having a thickness of 50 ⁇ m (trade name: A4100, manufactured by Toyobo Co., Ltd.) was used. Sheet 18 was obtained.
- the obtained pressure-sensitive adhesive sheets 1 to 7 and 12 to 17 were cut out to a size of 25 mm ⁇ 150 mm, and the polyester film that had been easily peeled off was peeled from the pressure-sensitive adhesive sheet to expose the pressure-sensitive adhesive layer.
- the layer is bonded to a copper foil (trade name: RCF-T58, manufactured by Fukuda Metal Foil Powder Industry Co., Ltd.) and pressure-bonded using a 2 kg roller, at room temperature and normal pressure (about 23 ° C., about 60% RH).
- the obtained pressure-sensitive adhesive sheets 8 to 11 and 18 were cut into a size of 25 mm ⁇ 150 mm, the polyester film subjected to the easy peeling treatment was peeled from the pressure-sensitive adhesive sheet to expose the pressure-sensitive adhesive layer, and the pressure-sensitive adhesive of the pressure-sensitive adhesive sheet
- the layer was bonded to a glass epoxy material having a thickness of 1.6 t (trade name: R1700, FR-4, manufactured by Panasonic Corporation), pressure-bonded using a 2 kg roller, and normal temperature and normal pressure (about 23 ° C., about 60%). RH) After leaving in an environment for 20 minutes, the adhesive force when the adhesive sheet was peeled from the glass epoxy material was measured under the same measurement conditions as above (initial adhesive force).
- the obtained pressure-sensitive adhesive sheets 8 to 11 and 18 were cut into a size of 100 mm ⁇ 100 mm, the polyester film subjected to the easy peeling treatment was peeled off from the pressure-sensitive adhesive sheet to expose the pressure-sensitive adhesive layer, and a glass having a thickness of 0.7 t. (Product name: Eagle XG, manufactured by Corning). 2. In a mixed acid of 50 ° C. (phosphoric acid 55%, acetic acid 30%, inorganic acid 5% or less, trade name: SEA-5, manufactured by Kanto Chemical Co., Inc.) so that the adhesive sheet / glass laminate is completely immersed.
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Abstract
Description
前記エポキシ熱硬化性樹脂が、前記アクリル樹脂に対して20質量%以上、60質量%以下の範囲で含まれてなることを特徴とするものである。
前記エポキシ熱硬化性樹脂が、前記アクリル樹脂に対して20質量%以上、60質量%以下の範囲で含まれてなることを特徴とするものである。
基材の一方の面側に、粘着剤組成物を塗布し、
前記粘着剤組成物を加熱して硬化させることにより粘着剤層を形成する、
ことを含んでなり、
前記粘着剤組成物が、アクリル樹脂と、エポキシ熱硬化性樹脂と、前記エポキシ熱硬化性樹脂を硬化させるための硬化剤と、を含んでなり、
前記エポキシ熱硬化性樹脂が、前記アクリル樹脂に対して20質量%以上、60質量%以下の範囲で含まれてなることを特徴とするものである。
前記粘着剤組成物の表面に離型シートを設けて、積層体を形成し、
前記積層体を加熱して、前記粘着剤組成物を硬化させることにより粘着剤層を形成する、
ことを含んでなることが好ましい。
本発明による粘着剤組成物は、アクリル樹脂とエポキシ熱硬化性樹脂と硬化剤とを必須成分として含む。以下、粘着剤組成物を構成する各成分について説明する。
本発明による粘着剤組成物を構成するアクリル樹脂は、(メタ)アクリル酸エステルを主成分とするアクリル樹脂を好適に使用できる。なお、本明細書において、(メタ)アクリル酸とは、アクリル酸および/またはメタクリル酸をいうものとする。(メタ)アクリル酸エステルとしては、メチルエステル、エチルエステル、プロピルエステル、イソプロピルエステル、ブチルエステル、イソブチルエステル、s-ブチルエステル、t-ブチルエステル、ペンチルエステル、イソペンチルエステル、ヘキシルエステル、ヘプチルエステル、オクチルエステル、2-エチルヘキシルエステル、イソオクチルエステル、ノニルエステル、イソノニルエステル、デシルエステル、イソデシルエステル、ウンデシルエステル、ドデシルエステル、トリデシルエステル、テトラデシルエステル、ヘキサデシルエステル、オクタデシルエステル、エイコシルエステル等の炭素数1~30、特に炭素数1~18の直鎖状または分岐状のアルキルエステル等の(メタ)アクリル酸アルキルエステル、および、シクロペンチルエステル、シクロヘキシルエステル等(メタ)アクリル酸シクロアルキルエステルを使用することができる。これらアクリル酸エステルは1種または2種以上を含んでいてもよい。
本発明による粘着剤組成物に用いられるエポキシ熱硬化性樹脂は、少なくとも1つ以上のエポキシ基またはグリシジル基を有するプレポリマーであって、硬化剤との併用により架橋重合反応により硬化し得るものであれば、特に制限なく使用することができる。このような熱硬化性のエポキシ樹脂を使用することにより、粘着剤組成物の耐薬品性を向上させることができ、その結果、被着体への貼合後に薬品処理等を行っても、浮きや剥がれの発生を抑制することができる。なお、本発明において、エポキシ熱硬化性樹脂とは、樹脂が硬化する前の前駆体または組成物を意味し、加熱によって硬化せしめたものをエポキシ熱硬化樹脂というものとする。本発明においては、エポキシ熱硬化性樹脂として、エポキシ当量が100g/eq.以上、2000g/eq.以下の範囲内にあるものを使用することが好ましい。エポキシ当量が100g/eq.未満のエポキシ熱硬化性樹脂では、架橋密度が高くなりすぎて粘着性が所望の範囲から低下してしまう場合があり、一方、2000g/eq.を超えるエポキシ熱硬化性樹脂では、粘着剤組成物を硬化させて粘着剤層を形成した際に、粘着剤層の耐熱性が不十分となる場合がある。なお、エポキシ当量は、JIS K7236に準拠した方法により測定した1グラム当量のエポキシ基を含む樹脂のグラム数である。
上記したエポキシ熱硬化性樹脂は加熱等により反応が進行して硬化するものであるが、本発明においては、硬化反応を促進するための硬化剤が粘着剤組成物中に含まれる。本発明においては、エポキシ樹脂と当量で反応する硬化剤としては、例えば、アミン系硬化剤、酸無水物系硬化剤、フェノール系硬化剤を好適に使用することができ、また、エポキシ樹脂を単独で硬化(重合)させ得る硬化剤としては、例えばイミダゾール系硬化剤やカチオン系硬化剤を好適に使用することができる。本発明においては、エポキシ樹脂の骨格由来の性能を期待でき、添加量が少なくてもエポキシ樹脂を単独で硬化させ得るイミダゾール系硬化剤やカチオン系硬化剤を使用することが好ましい。
本発明による粘着シートは、基材と基材の一方の面側に設けられた粘着剤層とを備えたものであり、粘着剤層として、上記した粘着剤組成物を熱硬化させたものを使用するものである。
<粘着剤組成物の調製>
モノマー単位として、メチルアクリレート、2-エチルヘキシルアクリレート、アクリル酸、2-ヒドロキシエチルアクリレートをそれぞれ質量基準で50:40:0.5:9.5の割合で含むアクリル共重合体樹脂(質量平均分子量20万、ガラス転移温度6℃)を用いた。このアクリル共重合体樹脂の酢酸エチル溶液(固形分35質量%)を100質量部と、液状エポキシ樹脂(ビスフェノールA型エポキシ樹脂、エポキシ当量:190g/eq.、分子量:370、商品名:jER828、三菱化学会社製)を14質量部と、硬化剤として2-エチル-4-メチルイミダゾール(商品名:キャアゾール2E4MZ、四国化成社製)を0.35質量部とを、トルエンおよびメチルエチルケトンの混合溶媒(商品名:KT-11,質量比1:1、DICグラフィクス社製)に溶解させ、ディスパーにて回転数500rpmで30分間撹拌した後、常温で気泡がなくなるまで放置することにより粘着剤組成物を得た。
モノマー単位として、メチルアクリレート、2-エチルヘキシルアクリレート、アクリル酸、2-ヒドロキシエチルアクリレートをそれぞれ質量基準で50:40:0.5:9.5の割合で含むアクリル共重合体樹脂(質量平均分子量20万、ガラス転移温度6℃)を用いた。このアクリル共重合体樹脂の酢酸エチル溶液(固形分35質量%)を100質量部と、固体状エポキシ樹脂(ビスフェノールA型エポキシ樹脂、エポキシ当量:480g/eq.、分子量:900、商品名:jER1001、三菱化学会社製)を14質量部と、硬化剤として2-メチル-4-エチルイミダゾール(商品名:キャアゾール2E4MZ、四国化成社製)を0.35質量部とを、トルエンおよびメチルエチルケトンの混合溶媒(商品名:KT-11,質量比1:1、DICグラフィクス社製)に溶解させ、ディスパーにて回転数500rpmで30分間撹拌した後、常温で気泡がなくなるまで放置することにより粘着剤組成物を得た。
得られた粘着剤組成物を、片面にシリコーン剥離剤による易剥離処理が施されている厚さ38μmのポリエステルフィルム(商品名:SP-PET-01、三井化学東セロ社製)の易剥離処理面上にアプリケータを用いて全面塗工した後、乾燥オーブンにより110℃で1分間乾燥し、厚さ10μmの粘着層を形成した。形成した粘着層の面に、厚さ25μmのポリイミドフィルム基材(商品名:カプトン100H、東レ・デュポン社製)をラミネートし、60℃で120時間養生することにより、粘着シート1を得た。
液状エポキシ樹脂および硬化剤の配合量を下記の表1に従って変更した以外は、実施例1と同様にして粘着シート2を得た。
実施例1で使用した液状エポキシ樹脂に代えて固体状エポキシ樹脂(ビスフェノールA型エポキシ樹脂、エポキシ当量:480g/eq.、分子量:900、商品名:jER1001、三菱化学会社製)を使用し、エポキシ樹脂および硬化剤の配合量を表1に従って変更した以外は、実施例1と同様にして粘着シート3を得た。
固体状エポキシ樹脂および硬化剤の配合量を下記の表1に従って変更した以外は、実施例3と同様にして粘着シート4を得た。
実施例1で使用した液状エポキシ樹脂に代えてアルコキシ基含有シラン変性エポキシ樹脂(固形分57質量%、エポキシ当量:1420g/eq.、分子量:2400、商品名:コンポセランE103D、荒川化学工業社製)を使用し、エポキシ樹脂および硬化剤の配合量を表1に従って変更した以外は、実施例1と同様にして粘着シート5を得た。
エポキシ樹脂および硬化剤の配合量を下記の表1に従って変更した以外は、実施例5と同様にして粘着シート6を得た。
実施例4において、粘着剤組成物に、架橋剤としてエポキシ架橋剤(固形分50質量%、商品名:E-5C、綜研化学社製)を0.2質量部加えた以外は、実施例4と同様にして粘着シート7を得た。
実施例4で使用した厚さ25μmのポリイミドフィルム基材に代えて、厚さ50μmのポリエステルフィルム基材(商品名:A4100、東洋紡社製)を使用した以外は、実施例4と同様にして粘着シート8を得た。
実施例8で使用した固体状エポキシ樹脂の一部を、下記の表1に従って、アルコキシ基含有シラン変性エポキシ樹脂(固形分57質量%、エポキシ当量:1420g/eq.、分子量:2400、商品名:コンポセランE103D、荒川化学工業社製)に変更し、硬化剤を1-ベンジル-2-メチルイミダゾール(商品名:キャアゾール1B2MZ、四国化成社製)に変更した以外は、実施例8と同様にして粘着シート9を得た。
実施例8で使用した固体状エポキシ樹脂の一部を、下記の表1に従って、アルコキシ基含有シラン変性エポキシ樹脂(固形分57質量%、エポキシ当量:1420g/eq.、分子量:2400、商品名:コンポセランE103D、荒川化学工業社製)に変更し、硬化剤を1-ベンジル-2-メチルイミダゾール(商品名:キャアゾール1B2MZ、四国化成社製)に変更した以外は、実施例8と同様にして粘着シート10を得た。
実施例8で使用した固体状エポキシ樹脂の一部を、下記の表1に従って、液状エポキシ樹脂(ビスフェノールA・エピクロルヒドリン・ダイマー酸の重縮合物、エポキシ当量:600~700g/eq.、商品名:jER872、三菱化学会社製)に変更し、硬化剤を1-ベンジル-2-メチルイミダゾール(商品名:キャアゾール1B2MZ、四国化成社製)に変更した以外は、実施例8と同様にして粘着シート11を得た。
固体状エポキシ樹脂および硬化剤の配合量を下記の表2に従って変更した以外は、実施例3と同様にして粘着シート12を得た。
固体状エポキシ樹脂および硬化剤の配合量を下記の表2に従って変更した以外は、実施例3と同様にして粘着シート13を得た。
エポキシ樹脂および硬化剤の配合量を下記の表2に従って変更した以外は、実施例5と同様にして粘着シート14を得た。
アクリル粘着剤(商品名:SK1439U、綜研化学社製)を100質量部と、硬化剤としてエポキシ架橋剤(固形分50質量%、商品名:E-5C、綜研化学社製)を0.6質量部とを、トルエンおよびメチルエチルケトンの混合溶媒(商品名:KT-11,質量比1:1、DICグラフィクス社製)151.5質量部に溶解させ、ディスパーにて回転数500rpmで30分間撹拌した後、常温で気泡がなくなるまで放置することにより粘着剤組成物を得た。
アクリル粘着剤(商品名:SK1439U、綜研化学社製)を100質量部と、硬化剤としてエポキシ架橋剤(固形分50質量%、商品名:E-5C、綜研化学社製)を0.6質量部と、固体状エポキシ樹脂(ビスフェノールA型エポキシ樹脂、商品名:jER1001、三菱化学会社製)を6質量部とを、トルエンおよびメチルエチルケトンの混合溶媒(商品名:KT-11,質量比1:1、DICグラフィクス社製)157.5質量部に溶解させ、ディスパーにて回転数500rpmで30分間撹拌した後、常温で気泡がなくなるまで放置することにより粘着剤組成物を得た。得られた粘着剤組成物を用いて、比較例4と同様にして粘着シート16を得た。
<粘着剤組成物の調製>
固形分が60質量%のシリコーン粘着剤(商品名:SD4600、東レ・ダウコーニング社製)を100質量部と、2種の硬化触媒(商品名:SRX212、およびBY24-741、いずれも東レ・ダウコーニング社製)をそれぞれ0.9質量部および1.5質量部とを、トルエンおよびメチルエチルケトンの混合溶媒(商品名:KT-11,質量比1:1、DICグラフィクス社製)100質量部に溶解させ、ディスパーにて回転数500rpmで30分間撹拌した後、常温で気泡がなくなるまで放置することにより粘着剤組成物を得た。
得られた粘着剤組成物を、厚さ25μmのポリイミドフィルム基材(商品名:カプトン100H、東レ・デュポン社製)の片面にアプリケータを用いて全面塗工した後、乾燥オーブンにより100℃で2分間乾燥し、厚さ10μmの粘着層を形成した。形成した粘着層の面に、厚さ40μmのポリプロピレンフィルム(商品名:トレファンBO-2500 #40)をラミネートすることにより、粘着シート17を得た。
比較例4で使用した厚さ25μmのポリイミドフィルム基材に代えて、厚さ50μmのポリエステルフィルム基材(商品名:A4100、東洋紡社製)を使用した以外は、比較例4と同様にして粘着シート18を得た。
得られた粘着シート1~7および12~17を、25mm×150mmのサイズに切り出し、易剥離処理が施されたポリエステルフィルムを粘着シートから剥離して粘着剤層を露出させ、粘着シートの粘着剤層を、銅箔(商品名:RCF-T58、福田金属箔粉工業社製)に貼合し、2kgのローラーを用いて圧着し、常温常圧(約23℃、約60%RH)環境下に20分間放置した後、引張試験機(型番:RTF-1150H、エー・アンド・デイ社製)を用いてJIS Z 0237に準拠した測定条件(引張速度:300mm/分、剥離距離:150mm、剥離角度:180度)により、粘着シートを銅箔から剥離する際の粘着力を測定した(初期粘着力)。また、粘着シートと銅箔とを貼合し、2kgのローラーを用いて圧着した後、230℃の環境下に60分間放置し、続いて常温常圧環境下に60分間放置した後の粘着力も上記と同様にして測定した(加熱処理後の粘着力)。さらに、銅箔に代えて板厚1.6tのガラスエポキシ材(商品名:R1700 FR-4、パナソニック社製)を使用し、上記と同様の条件にて初期粘着力および加熱処理後の粘着力を測定した。測定結果は下記の表1および2に示される通りであった。
得られた粘着シート8~11及び18を、100mm×100mmのサイズに切り出し、易剥離処理が施されたポリエステルフィルムを粘着シートから剥離して粘着剤層を露出させ、厚さ0.7tのガラス(商品名:Eagle XG、コーニング社製)に貼付した。その粘着シート/ガラス積層体が完全に浸漬するように、50℃の混酸(リン酸55%、酢酸30%、無機酸5%以下、商品名:SEA-5、関東化学社製)に2.5分間浸漬し、蒸留水で洗浄後に50℃の4%水酸化ナトリウムアルカリ水溶液に連続して各2.5間浸漬させた。その後、蒸留水により洗浄し、室温で乾燥させた。乾燥後の粘着シート/ガラス積層体における粘着シートの剥がれおよび粘着シート端部からの薬液の染み込みをマイクロスコープ(型番:VHX600、キーエンス社製)で確認した。剥がれが認められなかったものを○、剥がれが認められたものを×、薬液の染み込みが0.2mm未満であったものを○、薬液の染み込みが0.2mm以上であったものを×とした。評価結果は、下記の表1および2に示される通りであった。
Claims (8)
- アクリル樹脂と、エポキシ熱硬化性樹脂と、前記エポキシ熱硬化性樹脂を硬化させるための硬化剤と、を含んでなる粘着剤組成物であって、
前記エポキシ熱硬化性樹脂が、前記アクリル樹脂に対して20質量%以上、60質量%以下で含まれてなることを特徴とする、粘着剤組成物。 - 前記エポキシ熱硬化性樹脂のエポキシ当量が100g/eq.以上、2000g/eq.以下である、請求項1に記載の粘着剤組成物。
- 前記エポキシ熱硬化性樹脂の質量平均分子量が300以上、5000以下である、請求項1または2に記載の粘着剤組成物。
- 前記アクリル樹脂の質量平均分子量が10万以上、200万以下である、請求項1~3のいずれか一項に記載の粘着剤組成物。
- 基材と、前記基材の一方の面側に設けられた粘着剤層と、を備えてなる粘着シートであって、
前記粘着剤層が、アクリル樹脂と、エポキシ熱硬化性樹脂とを含んでなり、
前記エポキシ熱硬化性樹脂が、前記アクリル樹脂に対して20質量%以上、60質量%以下で含まれてなることを特徴とする、粘着シート。 - 前記粘着剤層の基材側とは反対の面側に、離型シートを備えてなる、請求項5に記載の粘着シート。
- 基材と、前記基材の一方の面側に設けられた粘着剤層と、を備えてなる粘着シートを製造する方法であって、
基材の一方の面側に、粘着剤組成物を塗布し、
前記粘着剤組成物を加熱して硬化させることにより粘着剤層を形成する、
ことを含んでなり、
前記粘着剤組成物が、アクリル樹脂と、エポキシ熱硬化性樹脂と、前記エポキシ熱硬化性樹脂を硬化させるための硬化剤と、を含んでなり、
前記エポキシ熱硬化性樹脂が、前記アクリル樹脂に対して20質量%以上、60質量%以下で含まれてなることを特徴とする、方法。 - 前記基材の一方の面側に粘着剤組成物を塗布して乾燥し、
前記粘着剤組成物の表面に離型シートを設けて、積層体を形成し、
前記積層体を加熱して、前記粘着剤組成物を硬化させることにより粘着剤層を形成する、
ことを含んでなる、請求項7に記載の方法。
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