Classifications

• • 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
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
  • C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
  • C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
  • C08G59/22—Di-epoxy compounds
  • C08G59/223—Di-epoxy compounds together with monoepoxy compounds
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
  • C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
  • C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
  • C08G59/50—Amines
  • C08G59/5046—Amines heterocyclic
  • C08G59/5053—Amines heterocyclic containing only nitrogen as a heteroatom
  • C08G59/5073—Amines heterocyclic containing only nitrogen as a heteroatom having two nitrogen atoms in the ring
• • 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
• • 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
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G2170/00—Compositions for adhesives
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
  • C08K5/0025—Crosslinking or vulcanising agents; including accelerators

Definitions

• the present invention relates to a one-component epoxy resin composition, and more specifically, to a one-component epoxy resin composition containing a specific epoxy compound, an epoxy resin, and an amine curing agent.
• Epoxy resins exhibit excellent properties in a wide range of applications such as adhesives, paints, electrical insulation materials, and civil engineering and construction materials.
• Epoxy resins commonly used, such as bisphenol-type epoxy resins often have high viscosity, and depending on the intended use, there may be problems with workability.
• Plasticizers can be used to improve workability, but plasticizers that do not participate in the reaction of epoxy resins will significantly reduce the physical properties after curing, so reactive diluents with epoxy groups are used in combination. It is often done.
• a reactive diluent having an epoxy group is required not to reduce the performance of the epoxy resin before dilution.
• Reactive diluents have been provided that suppress the physical properties of the cured product and reduce the viscosity of the resin.
• JP2006-083306A Japanese Patent Application Publication No. 2004-231787
• the problem to be solved by the present invention is to reduce the viscosity of epoxy resin without degrading its original performance as much as possible, and to provide reactivity that can provide new effects such as adhesiveness and storage stability.
• An object of the present invention is to provide an epoxy resin composition containing a diluent.
• the inventors of the present invention conducted extensive studies, discovered a one-component epoxy resin composition containing a specific epoxy compound, an epoxy resin, and an amine curing agent, and arrived at the present invention. That is, the present invention provides a one-component epoxy resin composition comprising (A) component: a compound represented by the following general formula (1), (B) component: epoxy resin, and (C) component: amine curing agent. It is.
• R 1 represents a hydrogen atom or a methyl group
• R 2 and R 3 each independently represent a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, or a carbon atom number. It represents an alkoxy group of 1 to 6, and n represents an integer of 1 to 3.
• the one-component epoxy resin composition of the present invention has a low viscosity and has excellent storage stability when used in combination with an amine curing agent, and is also resistant to gold and engineering plastics, which are difficult to adhere to with conventional techniques. Since it has excellent adhesive properties, it can be suitably used in electronic material applications where such materials are used.
• the component (A) in the one-component epoxy resin composition of the present invention is a compound represented by the following general formula (1).
• R 1 represents a hydrogen atom or a methyl group
• R 2 and R 3 each independently represent a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, or a carbon atom number. It represents an alkoxy group of 1 to 6, and n represents an integer of 1 to 3.
• R 1 in general formula (1) is preferably a hydrogen atom from the viewpoint of reactivity.
• Examples of the alkyl group having 1 to 6 carbon atoms represented by R 2 and R 3 in general formula (1) include methyl group, ethyl group, propyl group, iso-propyl group, butyl group, sec-butyl group, tert -butyl group, iso-butyl group, amyl group, iso-amyl group, tert-amyl group, hexyl group, and the like.
• examples of the alkoxy group having 1 to 6 carbon atoms represented by R 2 and R 3 in general formula (1) include groups in which the alkyl group listed above is bonded to an oxygen atom.
• R 2 and R 3 in general formula (1) are preferably a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, from the viewpoint of more easily exerting the effects of the present invention, and are hydrogen atoms. is more preferable. Further, R 2 and R 3 may be the same or different, but are preferably the same from the viewpoint of more easily exerting the effects of the present invention.
• the method for producing the compound represented by the general formula (1) used in the present invention is not particularly limited, but for example, styrenated phenol is epoxied by epichlorohydrin or methylepichlorohydrin (hereinafter referred to as epichlorohydrin).
• epichlorohydrin methylepichlorohydrin
• Styrenated phenol can be obtained by adding styrene to phenol in combination with an acidic catalyst such as AlCl 3 .
• an acidic catalyst such as AlCl 3 .
• the number of n represented by general formula (1) is determined.
• n is an integer from 1 to 3, preferably from 1 to 2.
• the compound represented by the general formula (1) may be a mixture of compounds in which n is different, and in that case, from the viewpoint of low viscosity, the average value of n is 1.2 to 1.5. It is preferable. Further, from the viewpoint of developing high adhesiveness, it is preferable that the average value of n is 2.8 to 3.0. Furthermore, from the viewpoint of achieving both low viscosity and high adhesiveness, it is preferable that the average value of n is 2.2 to 2.6.
• phase transfer catalyst examples include tetramethylammonium salt, tetrabutylammonium salt, and the like.
• phase transfer catalyst it is preferable to use 0.001 to 0.1 mol of the phase transfer catalyst per 1 mol of styrenated phenol.
• the compound represented by the general formula (1) obtained by the above method etc. can be obtained by oil/water separation using water or an organic solvent, filtration, concentration, distillation, extraction, crystallization, recrystallization, adsorption, column chromatography, etc. Separation and purification may be performed by means of separation and purification, or a combination of these means.
• the epoxy equivalent of the compound represented by general formula (1) is 250 to 500 g/eq. is preferably 280 to 480 g/eq. It is more preferable that Note that the epoxy equivalent can be measured in accordance with JIS K 7236:2001 (corresponding to ISO3001:1999). From the viewpoint of low viscosity, the epoxy equivalent of the compound represented by general formula (1) is 250 to 350 g/eq. is preferably 280 to 330 g/eq. It is more preferable that In addition, from the viewpoint of achieving both low viscosity and high adhesiveness, the epoxy equivalent of the compound represented by general formula (1) is 330 to 450 g/eq. is preferably 350 to 420 g/eq. It is more preferable that Furthermore, from the viewpoint of developing high adhesiveness, the epoxy equivalent of the compound represented by general formula (1) is 400 to 500 g/eq. is preferably 420 to 480 g/eq. It is more preferable that
• the viscosity of the compound represented by general formula (1) at 25° C. is preferably 10 mPa ⁇ s to 300 Pa ⁇ s, more preferably 100 mPa ⁇ s to 200 Pa ⁇ s.
• the viscosity may be appropriately selected depending on the application, but when low viscosity is preferred, the viscosity of the compound represented by general formula (1) at 25 ° C. is preferably 50 to 500 mPa s, More preferably, it is 100 to 250 mPa ⁇ s. Further, when it is desirable to have both low viscosity and high adhesiveness, the viscosity at 25° C. is preferably 1000 to 5000 mPa ⁇ s, more preferably 1500 to 3000 mPa ⁇ s.
• the viscosity at 25° C. is preferably 10 to 300 Pa ⁇ s, more preferably 50 to 200 Pa ⁇ s.
• the viscosity can be measured with a cone-plate rotational viscometer (E-type viscometer).
• the viscosity measurement conditions differ depending on the target sample. Specifically, when measuring 50 to 500 mPa, an E-type viscometer (using a 1° 34' x R24 cone rotor) and a microwave oven are used. H, rotation speed 20 rpm, and 25°C. When measuring 1000 to 5000 mPa, use an E-type viscometer (using a 3° x R14 cone rotor), range H, rotation speed 10 rpm, and 25°C. When measuring 50 to 200 Pa, use an E-type viscometer (using a 3° x R14 cone rotor), range U, rotation speed 2.5 rpm, and 25°C.
• the total amount of chlorine in the compound represented by general formula (1) is preferably 0 to 3000 ppm, more preferably 0 to 1500 ppm. Note that the total chlorine amount can be measured by a combustion-coulometric method.
• Examples of the epoxy resin as component (B) in the one-component epoxy resin composition of the present invention include polyglycidyl etherified mononuclear polyhydric phenol compounds such as hydroquinone, resorcinol, pyrocatechol, and phloroglucinol; dihydroxynaphthalene; , biphenol, methylene bisphenol (bisphenol F), methylene bis (orthocresol), ethylidene bisphenol, isopropylidene bisphenol (bisphenol A), isopropylidene bis (orthocresol), tetrabromo bisphenol A, 1,3-bis(4-hydroxycresol) milbenzene), 1,4-bis(4-hydroxycumylbenzene), 1,1,3-tris(4-hydroxyphenyl)butane, 1,1,2,2-tetra(4-hydroxyphenyl)ethane, Polyglycidyl etherified products of polynuclear polyhydric phenol compounds such as thiobis
• Polyglycidyl ethers of polyhydric alcohols maleic acid, fumaric acid, itaconic acid, succinic acid, glutaric acid, suberic acid, adipic acid, azelaic acid, sebacic acid, dimer acid, trimer acid, phthalic acid, isophthalic acid, terephthalic acid , glycidyl esters of aliphatic, aromatic or alicyclic polybasic acids such as trimellitic acid, trimesic acid, pyromellitic acid, tetrahydrophthalic acid, hexahydrophthalic acid, endomethylenetetrahydrophthalic acid, and homopolymerized glycidyl methacrylate.
• N,N-diglycidylaniline bis(4-(N-methyl-N-glycidylamino)phenyl)methane, diglycidyl orthotoluidine, N,N-bis(2,3-epoxypropyl) -4-(2,3-epoxypropoxy)-2-methylaniline, N,N-bis(2,3-epoxypropyl)-4-(2,3-epoxypropoxy)aniline, N,N,N', Epoxy compounds having a glycidylamino group such as N'-tetra(2,3-epoxypropyl)-4,4'-diaminodiphenylmethane; vinylcyclohexene diepoxide, dicyclopentanediene diepoxide, 3,4-epoxycyclohexylmethyl- Epoxy of cyclic olefin compounds such as 3,4-epoxycyclohexanecarboxylate, 3,4-
• Examples include epoxidized polybutadiene, epoxidized conjugated diene polymers such as epoxidized styrene-butadiene copolymer, and heterocyclic compounds such as triglycidyl isocyanurate. These may be used alone or in combination of two or more.
• bisphenol-type epoxy resins are preferred because they are easily available and the cured product has good physical properties.
• component (A) has the effect of reducing the viscosity and also has the effect of improving the performance as an adhesive for various base materials, but if the content is too small, There is a possibility that the effects of viscosity reduction and adhesive performance cannot be obtained, and if the content is too large, other performances (heat resistance and elastic modulus) of the composition may decrease.
• the content of component (A) is preferably 1 to 50% by mass, more preferably 10 to 50% by mass, and 20 to 40% by mass based on the total mass of components (A) and (B). Mass % is even more preferred.
• amine curing agent which is component (C) in the one-component epoxy resin composition of the present invention
• known ones can be used, such as ethylenediamine, 1,2-diaminopropane, 1,3-diaminopropane.
• Component (C) is preferably an amine-based latent curing agent in order to further improve the storage stability of the composition.
• An amine-based latent curing agent is a curing agent that has an amino group in its structure and exhibits small changes in viscosity and physical properties at room temperature when mixed with a compound containing an epoxy group.
• the one-component epoxy resin composition of the present invention has excellent storage stability compared to conventional compositions containing an epoxy resin and an amine-based latent curing agent. .
• Examples of the amine-based latent curing agent include dicyandiamide type, imidazole type, polyamine type and polyurea type latent curing agents.
• Examples of the dicyandiamide-type latent curing agent include dicyandiamide alone, or, if necessary, in combination with a curing accelerator described below.
• the imidazole-type latent curing agent can be obtained, for example, by reacting an epoxy compound with an imidazole compound containing active hydrogen at 50 to 150°C for 1 to 20 hours using a solvent as necessary. Can be done. When a solvent is used, after the reaction is completed, the solvent is removed at 80 to 200° C. under normal pressure or reduced pressure.
• imidazole compounds used in the production of imidazole-type latent curing agents include 2-methylimidazole, 2-ethyl-4-methylimidazole, 2-undecylimidazole, 2-heptadecylimidazole, and 2-phenylimidazole. Can be mentioned.
• Examples of the epoxy compound used in the production of the imidazole type latent curing agent include the epoxy compounds exemplified as component (B).
• Solvents used in the production of imidazole-type latent curing agents include ketones such as methyl ethyl ketone, methyl amyl ketone, diethyl ketone, acetone, methyl isopropyl ketone, propylene glycol monomethyl ether acetate, and cyclohexanone; tetrahydrofuran, 1,2-dimethoxyethane , 1,2-diethoxyethane, propylene glycol monomethyl ether, and other ethers; ethyl acetate, n-butyl acetate, and other esters; benzene, toluene, xylene, and other aromatic hydrocarbons; carbon tetrachloride, chloroform, trichloroethylene, Examples include halogenated aliphatic hydrocarbons such as methylene chloride; halogenated aromatic hydrocarbons such as chlorobenzene.
• a polyamine-type latent curing agent can be obtained, for example, by reacting an epoxy compound with a polyamine at 50 to 150°C for 1 to 20 hours, using a solvent as necessary. When a solvent is used, after the reaction is completed, the solvent is removed at 80 to 200° C. under normal pressure or reduced pressure.
• Examples of the polyamine used in the production of the polyamine-type latent curing agent include those having two or more active hydrogens among the amine compounds exemplified as amine-based curing agents. These may be used alone or in combination of two or more.
• Examples of the epoxy compound used in the production of the polyamine type latent curing agent include the epoxy compounds exemplified as component (B).
• a polyurea-type latent curing agent can be obtained, for example, by reacting a polyisocyanate with a polyamine at 50 to 150°C for 1 to 20 hours, using a solvent if necessary. When a solvent is used, after the reaction is completed, the solvent is removed at 80 to 200° C. under normal pressure or reduced pressure.
• Examples of the polyamine used in the production of the polyurea-type latent curing agent include those having two or more active hydrogens among the amine compounds exemplified as amine-based curing agents.
• Polyisocyanates used in the production of polyurea-type latent curing agents include aromatic diisocyanates such as phenylene diisocyanate, tolylene diisocyanate, diphenylmethane diisocyanate, naphthalene diisocyanate, and xylylene diisocyanate, hexamethylene diisocyanate, lysine diisocyanate, cyclohexane diisocyanate, and isophorone.
• NCO group blocking agents include active methylene compounds such as malonate diesters (diethyl malonate, etc.), acetylacetone, acetoacetate (ethyl acetoacetate, etc.); acetoxime, methyl ethyl ketoxime (MEK oxime), methyl isobutyl ketox.
• active methylene compounds such as malonate diesters (diethyl malonate, etc.), acetylacetone, acetoacetate (ethyl acetoacetate, etc.); acetoxime, methyl ethyl ketoxime (MEK oxime), methyl isobutyl ketox.
• Oxime compounds such as oxime (MIBK oxime); monohydric alcohols such as methyl alcohol, ethyl alcohol, propyl alcohol, butyl alcohol, heptyl alcohol, hexyl alcohol, octyl alcohol, 2-ethylhexyl alcohol, isononyl alcohol, stearyl alcohol, etc.; Isomers; glycol derivatives such as methyl glycol, ethyl glycol, ethyl diglycol, ethyl triglycol, butyl glycol, butyl diglycol; amine compounds such as dicyclohexylamine; phenol, cresol, ethylphenol, n-propylphenol, isopropylphenol, Monophenols such as butylphenol, tert-butylphenol, octylphenol, nonylphenol, dodecylphenol, cyclohexylphenol, chlorophenol, and bromophenol; diphenols such as
• phenolic resins may be used in combination to improve the storage stability of the composition.
• the amount of phenolic resin used in combination is, for example, 10 to 50% by mass based on the total mass of the amine latent curing agent.
• phenolic resins include phenol novolak resin, cresol novolak resin, aromatic hydrocarbon formaldehyde resin-modified phenol resin, dicyclopentadiene phenol addition type resin, phenol aralkyl resin (Zyrock resin), naphthol aralkyl resin, and trisphenylolmethane.
• Resin tetraphenylolethane resin, naphthol novolak resin, naphthol-phenol co-condensed novolak resin, naphthol-cresol co-condensed novolak resin, biphenyl-modified phenol resin (polyhydric phenol compound with phenol cores linked by bismethylene groups), biphenyl-modified resin Naphthol resin (a polyvalent naphthol compound in which a phenol nucleus is linked with a bismethylene group), aminotriazine-modified phenol resin (a compound having a phenol skeleton, a triazine ring, and a primary amino group in its molecular structure), and an alkoxy group-containing aromatic ring
• Polyhydric phenol compounds such as modified novolac resins (polyhydric phenol compounds in which a phenol nucleus and an alkoxy group-containing aromatic ring are linked with formaldehyde) are mentioned.
• a commercially available amine-based latent curing agent may be used, such as ADEKA HARDNER EH-3636AS (manufactured by ADEKA Corporation; dicyandiamide type latent hardening agent), ADEKA HARDNER EH-4351S (manufactured by ADEKA Corporation; dicyandiamide-type latent hardener), ADEKA Hardener EH-5011S (manufactured by ADEKA Corporation; imidazole-type latent hardener), ADEKA Hardner EH-5046S (manufactured by ADEKA Corporation; imidazole-type latent hardener), ADEKA HARDNER EH-4357S (manufactured by ADEKA Co., Ltd.; polyamine type latent curing agent), ADEKA Hardener EH-5057P (manufactured by ADEKA Co., Ltd.; polyamine type latent curing agent), ADEKA Hardener EH-5057PK (manufactured
• the content of component (C) in the one-component epoxy resin composition of the present invention is preferably 1 to 100 parts by mass, and 5 to 70 parts by mass based on 100 parts by mass of the total mass of components (A) and (B). part is more preferable.
• the one-component epoxy resin composition of the present invention may contain a curing accelerator.
• a curing accelerator By using component (C) and a curing accelerator together, the curing speed can be improved.
• the curing accelerator include phosphines such as triphenylphosphine; phosphonium salts such as tetraphenylphosphonium bromide; amines such as benzyldimethylamine and 2,4,6-tris(dimethylaminomethyl)phenol; trimethylammonium chloride.
• Quaternary ammonium salts such as; 3-(p-chlorophenyl)-1,1-dimethylurea, 3-(3,4-dichlorophenyl)-1,1-dimethylurea, 3-phenyl-1,1-dimethylurea, Examples include ureas such as isophorone diisocyanate-dimethylurea and tolylene diisocyanate-dimethylurea; and complex compounds of boron trifluoride and amines, ether compounds, etc.
• These curing accelerators may be used alone or in combination of two or more.
• the content of the curing accelerator is not particularly limited and can be appropriately set depending on the use of the one-component epoxy resin composition of the present invention.
• the curing accelerator may be of a core-shell type, and specifically, as described in Japanese Patent Publication No. 07-005708, Japanese Patent No. 4405741, etc., a solid tertiary amine is used as a core component and an epoxy resin is used.
• Examples include masterbatch-type curing accelerators in which a shell made of a reaction product of an amine compound and an amine compound is dispersed in an epoxy resin. From the viewpoint of storage stability of the epoxy resin composition, these curing accelerators are preferably used in combination with a thiol curing agent or an acid anhydride.
• masterbatch type curing accelerator commercially available products may be used, such as HX-3742, HX-3721, HXA9322HP, HXA3922HP, HXA3932HP, HXA5945HP, HXA9382HP, etc. in the Novacure series manufactured by Asahi Kasei Corporation. It will be done.
• An inorganic filler may be added to the one-component epoxy resin composition of the present invention, if necessary.
• examples of such inorganic fillers include silica such as fused silica, crystalline silica, and fumed silica, magnesium hydroxide, aluminum hydroxide, zinc borate, zinc molybdate, calcium carbonate, silicon nitride, silicon carbide, and boron nitride.
• examples include powders of calcium silicate, potassium titanate, aluminum nitride, beryllia, zirconia, zircon, forsterite, steatite, spinel, mullite, titania, beads made of these powders, and glass fibers.
• the one-component epoxy resin composition of the present invention may contain additives other than the above-mentioned inorganic filler, if necessary.
• additives include, for example, silane coupling agents; non-reactive diluents (plasticizers) such as dioctyl phthalate, dibutyl phthalate, benzyl alcohol, and coal tar; glass fibers, pulp fibers, synthetic fibers, ceramic fibers, etc.
• Fibrous fillers such as glass cloth, aramid cloth, and carbon fiber; pigments; candelilla wax, carnauba wax, Japanese wax, privet wax, beeswax, lanolin, spermaceti wax, montan wax, petroleum wax, aliphatic wax, Lubricants such as aliphatic esters, aliphatic ethers, aromatic esters, and aromatic ethers; thickeners; thixotropic agents; antioxidants; light stabilizers; ultraviolet absorbers; flame retardants; antifoaming agents; rust inhibitors ;Commonly used additives such as colloidal silica and colloidal alumina can be mentioned.
• adhesive resins such as xylene resins and petroleum resins can also be used in combination.
• the one-component epoxy resin composition of the present invention preferably has a small total chlorine amount from the viewpoint of reliability under high temperature and high humidity conditions.
• the total chlorine amount is preferably 3000 ppm or less, and 1500 ppm or less. It is more preferable that it is below. Since it is preferable that the total amount of chlorine is small, the ideal value of the total amount of chlorine is 0 ppm.
• the total chlorine amount can be measured by combustion-coulometric method.
• the one-component epoxy resin composition of the present invention preferably has a viscosity of 2.0 to 50 Pa ⁇ s at 25°C, more preferably 2.0 to 30 Pa ⁇ s. Note that the viscosity can be measured with a cone-plate rotational viscometer (E-type viscometer).
• the one-component epoxy resin composition of the present invention is produced by stirring, melting, mixing, and dispersing components (A) to (C) and any optional components added as necessary, with heat treatment as necessary. can do.
• the equipment used for stirring, melting, mixing, and dispersion is not particularly limited, and in the present invention, a Raikai machine equipped with a stirrer and a heating device, a three-roll mill, a ball mill, a planetary mixer, Bead mills, planetary stirrers, etc. can be used. Further, these devices may be used in combination as appropriate.
• the one-component epoxy resin composition of the present invention can be suitably used as an adhesive.
• base materials to which adhesives can be applied include base materials made of glass, metal, leather, wood materials, thermoplastic resins, fiber-reinforced plastics, and the like.
• base materials metal base materials and thermoplastic resin base materials are preferred, and metal base materials are more preferred.
• metals include iron, aluminum, steel, copper, magnesium, and titanium, and alloys of these metals with other non-ferrous metals.
• aluminum is preferred.
• the surface of the metal base material may be plated.
• Examples of the types of plating include chrome plating, hard chrome plating, nickel plating, electroless nickel plating, zinc plating, gold plating, and silver plating.
• the one-component epoxy resin composition of the present invention can be particularly suitably used as an adhesive for nickel-plated or gold-plated metal substrates.
• thermoplastic resin examples include vinyl chloride resin, polystyrene, polyester, polyamide, polyurethane, polyethylene, polypropylene, polyphenylene ether, polycarbonate, polyether sulfone, polysulfone, polyphenylene sulfone, polyphenylene sulfide, polyether ether ketone, and liquid crystal.
• examples include polymers.
• the adhesive made of the one-component epoxy resin composition of the present invention has good adhesion to various base materials, it can be used between the same type of base materials selected from the above-mentioned base materials or between different base materials. It can be used as an adhesive for joining.
• the one-component epoxy resin composition of the present invention can be used as laminates for printed wiring boards, interlayer insulation materials for build-up boards, adhesive films for build-ups, die attach agents, and underfills for flip-chip mounting.
• Resin materials for electronic circuit boards such as materials, grab top materials, liquid sealants for TCP, conductive adhesives, liquid crystal sealants, coverlays for flexible boards, and resist inks; Semiconductor sealing materials; optical waveguides and optical films, etc. optical materials; resin casting materials; various optical semiconductor devices such as LEDs, phototransistors, photodiodes, photocouplers, CCDs, EPROMs, and photosensors; applicable to various uses such as fiber-reinforced resin molded products such as CFRP can do.
• the internal pressure was reduced to 150 to 200 hPa, and 166.88 g of a 48% aqueous sodium hydroxide solution (sodium hydroxide: 0.96 mol) was placed in the dropping device.
• a 48% aqueous sodium hydroxide solution was added dropwise over 1 hour, and water generated by the reaction during the addition and water present in the aqueous sodium hydroxide solution was removed by azeotropic dehydration.
• the reaction was continued for another 2 hours, and after confirming that the water in the system had been completely removed, the solution was heated to 120 to 130°C, and excess epichlorohydrin was removed by applying normal pressure and reduced pressure.
• the epoxy equivalent of the reactant in the system was 317 g/eq, and the amount of saponifiable chlorine was 0.65%.
• the inside of the system was cooled to 60° C., 300 g of toluene and 200 g of ion-exchanged water were added, and oil and water were separated.
• a toluene solution of the crude epoxy compound was obtained after performing the oil/water separation three times.
• a toluene solution of the obtained crude epoxy compound was placed in a flask equipped with a reflux device, a stirring device, and a dropping device, and 11.46 g of a 48% aqueous sodium hydroxide solution and 15 g of ion-exchanged water were added thereto, and the mixture was heated at 65°C for 30 minutes. Stir for 1 minute. Thereafter, 0.18 g (0.81 mmol) of benzyltriethylammonium chloride was added to the reaction solution, and the reaction was further carried out at 65° C. for 2 hours. Thereafter, oil and water separation using toluene/ion-exchanged water, solvent removal, and filtration were performed to obtain epoxy compound 1.
• Epoxy compound 1 contains, as a main component, a compound in which R 1 , R 2 , and R 3 are all hydrogen atoms and the average value of n is 1.3 in general formula (1).
• the epoxy equivalent of epoxy compound 1 was 305 g/eq, the viscosity at 25° C. was 186 mPa ⁇ s, the saponifiable chlorine amount was 143 ppm, and the total chlorine amount was 755 ppm.
• the viscosity was measured using a cone-plate rotational viscometer (E-type viscometer), the saponifiable chlorine amount was measured in accordance with JIS K 7243, and the total chlorine amount was measured by combustion-coulometric method.
• Epoxy compound 2 includes, as a main component, a compound in which R 1 , R 2 , and R 3 are all hydrogen atoms and the average value of n is 2.4 in general formula (1).
• the epoxy equivalent of epoxy compound 2 was 378 g/eq, the viscosity at 25° C. was 2332 mPa ⁇ s, the saponifiable chlorine amount was 290 ppm, and the total chlorine amount was 730 ppm.
• Epoxy compound 3 includes, as a main component, a compound in which R 1 , R 2 , and R 3 are all hydrogen atoms and the average value of n is 3 in general formula (1).
• the epoxy equivalent of epoxy compound 2 was 460 g/eq, the viscosity at 25° C. was 95 Pa ⁇ s, the saponifiable chlorine amount was 210 ppm, and the total chlorine amount was 640 ppm.
• Example 1 One-component epoxy resin compositions were prepared with the formulations (parts by mass) shown in Table 1, and the storage stability of each composition at 25°C and 40°C was evaluated. The evaluation method was to calculate the rate of increase in viscosity (%) after storage for 1 day and 7 days in a constant temperature bath at the respective temperature, based on the viscosity of each composition immediately after blending. .
• the materials used in the formulation are as follows.
• B) Component EP-4100E: Bisphenol A epoxy resin, manufactured by ADEKA Co., Ltd.
• Component EP-4088L Dicyclopentadiene epoxy resin
• Component (C) EH-5046S Imidazole type latent curing agent, manufactured by ADEKA Co., Ltd.
• the one-component epoxy resin composition of the present invention was compared with Comparative Example 1 in which EP-4088L, a dicyclopentadiene-type epoxy resin known as a material that has the effect of diluting epoxy resin, was blended. It was found that they had the same viscosity and had excellent storage stability in both the 25°C and 40°C temperature ranges.
• the shear strength was measured as follows. A silicone sheet with holes of 4 mm in diameter and 1 mm in height was placed on each base material, and the resin composition was poured into the holes. This was cured at 150° C. for 2 hours to produce a cylindrical molded product with a diameter of 4 mm and a height of 1 mm. Thereafter, the shear strength (MPa) was measured using a 4000Plus bond tester (manufactured by Nordson DAGE). The following materials were used for each base material.
• Au base material Gold plated SPCC-SB (manufactured by Engineering Test Service Co., Ltd.)
• PPS base material Susteel GS-40 (manufactured by Test Piece Co., Ltd.)
• Ni base material Ni plating SPCC-SB (manufactured by Test Piece Co., Ltd.)
• Al base material A5052P (manufactured by Test Piece Co., Ltd.)
• Cu base material C1100 (manufactured by Engineering Test Service Co., Ltd.)
• the one-component epoxy resin composition of the present invention has superior shear strength on any of the base materials of Au, PPS, Ni, Al, and Cu, compared to the resin composition that does not use epoxy compound 1. I found out that

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• 2023
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