WO2017037951A1 - Composition adhésive, composition adhésive électroconductrice de façon anisotrope, matériau de connexion de circuit, et objet connecté - Google Patents

Composition adhésive, composition adhésive électroconductrice de façon anisotrope, matériau de connexion de circuit, et objet connecté Download PDF

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Publication number
WO2017037951A1
WO2017037951A1 PCT/JP2015/075253 JP2015075253W WO2017037951A1 WO 2017037951 A1 WO2017037951 A1 WO 2017037951A1 JP 2015075253 W JP2015075253 W JP 2015075253W WO 2017037951 A1 WO2017037951 A1 WO 2017037951A1
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WIPO (PCT)
Prior art keywords
circuit
adhesive composition
meth
epoxy resin
adhesive
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PCT/JP2015/075253
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English (en)
Japanese (ja)
Inventor
直 工藤
藤縄 貢
暁黎 杜
伊藤 彰浩
智樹 森尻
Original Assignee
日立化成株式会社
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Application filed by 日立化成株式会社 filed Critical 日立化成株式会社
Priority to PCT/JP2015/075253 priority Critical patent/WO2017037951A1/fr
Priority to CN201580082812.8A priority patent/CN107922817B/zh
Priority to KR1020187008753A priority patent/KR102376223B1/ko
Priority to JP2017537184A priority patent/JP6631631B2/ja
Publication of WO2017037951A1 publication Critical patent/WO2017037951A1/fr

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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J163/00Adhesives based on epoxy resins; Adhesives based on derivatives of epoxy resins
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J9/00Adhesives characterised by their physical nature or the effects produced, e.g. glue sticks
    • C09J9/02Electrically-conducting adhesives
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J11/00Features of adhesives not provided for in group C09J9/00, e.g. additives
    • C09J11/02Non-macromolecular additives
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J201/00Adhesives based on unspecified macromolecular compounds
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B1/00Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
    • H01B1/20Conductive material dispersed in non-conductive organic material
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01RELECTRICALLY-CONDUCTIVE CONNECTIONS; STRUCTURAL ASSOCIATIONS OF A PLURALITY OF MUTUALLY-INSULATED ELECTRICAL CONNECTING ELEMENTS; COUPLING DEVICES; CURRENT COLLECTORS
    • H01R11/00Individual connecting elements providing two or more spaced connecting locations for conductive members which are, or may be, thereby interconnected, e.g. end pieces for wires or cables supported by the wire or cable and having means for facilitating electrical connection to some other wire, terminal, or conductive member, blocks of binding posts
    • H01R11/01Individual connecting elements providing two or more spaced connecting locations for conductive members which are, or may be, thereby interconnected, e.g. end pieces for wires or cables supported by the wire or cable and having means for facilitating electrical connection to some other wire, terminal, or conductive member, blocks of binding posts characterised by the form or arrangement of the conductive interconnection between the connecting locations

Definitions

  • the present invention relates to an adhesive composition, an anisotropic conductive adhesive composition, a circuit connection material, and a connection body.
  • various adhesive compositions are conventionally used as a circuit connection material for the purpose of bonding various members in the element.
  • the adhesive composition is required to have various properties such as adhesiveness, heat resistance, reliability in a high temperature and high humidity state, and the like.
  • the adherends to be bonded are various surfaces formed from various materials such as printed wiring boards, organic materials such as polyimide films, metals such as copper and aluminum, and metal compounds such as ITO, SiN and SiO 2. Have Therefore, the adhesive composition is designed according to each adherend.
  • thermosetting resin composition containing a thermosetting resin such as an epoxy resin having high adhesion and high reliability is known (for example, Patent Document 1). reference).
  • Such an adhesive composition generally contains an epoxy resin, a curing agent such as a phenol resin that reacts with the epoxy resin, and a thermal latent catalyst that promotes the reaction between the epoxy resin and the curing agent.
  • the thermal latent catalyst is an important factor that determines the curing temperature and the curing rate. For this reason, various compounds are used as thermal latent catalysts from the viewpoint of storage stability at room temperature and curing rate during heating.
  • This adhesive composition is generally cured by heating at a temperature of 170 to 250 ° C. for 1 to 3 hours to exhibit a desired adhesive property.
  • radical curable adhesive containing a (meth) acrylate derivative and a peroxide has attracted attention (see, for example, Patent Document 2).
  • the radical curable adhesive is advantageous in terms of short-time curing because radicals which are reactive active species are rich in reactivity.
  • Patent Document 3 discloses a radical curable adhesive containing a (meth) acrylate compound having an epoxy group in the molecule.
  • thermosetting resin composition In order to achieve low temperature rapid curing of the adhesive composition, for example, in the above thermosetting resin composition, a thermal latent catalyst having a low activation energy may be used. It is very difficult to maintain storage stability.
  • radical curing type adhesives can achieve low temperature rapid curing relatively easily.
  • a connection body obtained using a radical curable adhesive is exposed to a high-temperature and high-humidity environment, the interface between the circuit member and the adhesive often peels off and bubbles are often generated.
  • the radical curable adhesive tends to cause large curing shrinkage as compared with an adhesive containing an epoxy resin.
  • Patent Document 3 discloses a radical curable adhesive containing a (meth) acrylate compound having an epoxy group in the molecule.
  • this adhesive for example, in connection conditions at a low temperature of 140 ° C.
  • the adhesiveness to the adherend was insufficient, and the generation of bubbles due to peeling of the interface between the circuit member and the adhesive could not be completely suppressed after the high temperature and high humidity test.
  • the present invention has been made in view of the above-mentioned problems of the prior art. Even though it is a radical curable adhesive, it can be used even at low temperature (for example, 140 ° C. or less) and for a short time (for example, 5 seconds or less). It is an object of the present invention to provide an adhesive composition that can maintain sufficient adhesive strength and connection reliability and can suppress peeling from an adherend under high temperature and high humidity conditions.
  • the present invention includes (a) a thermoplastic resin, (b) a radical polymerizable compound, (c) a radical polymerization initiator, and (d) an epoxy resin having no (meth) acryloyloxy group,
  • An adhesive composition substantially free from the cationic polymerization curing agent is provided. According to such an adhesive composition, sufficient adhesive strength and connection reliability are maintained even under low temperature (for example, 140 ° C. or less) and short time (for example, 5 seconds or less) connection conditions, and high temperature and high humidity conditions. It becomes possible to suppress peeling from the adherend.
  • the epoxy resin preferably has a biphenyl skeleton. By including an epoxy resin having such a skeleton, the above-described effects are further increased.
  • the adhesive composition of the present invention may further contain (e) conductive particles.
  • the adhesive composition can be imparted with conductivity or anisotropic conductivity, so that the adhesive composition can be more suitably used as a circuit connection material.
  • the connection resistance between the circuit electrodes electrically connected via the adhesive composition can be more easily reduced.
  • the present invention also includes (a) a thermoplastic resin, (b) a radically polymerizable compound, (c) a radical polymerization initiator, (d) an epoxy resin having no (meth) acryloyloxy group, and (e) a conductive material.
  • a thermoplastic resin e.g., polyethylene glycol dimethacrylate copolymer
  • a radical polymerization initiator e.g., a radical polymerization initiator
  • an epoxy resin having no (meth) acryloyloxy group e.
  • An anisotropic conductive adhesive composition containing particles and substantially free of an epoxy resin cationic polymerization curing agent is provided.
  • the epoxy resin preferably has a biphenyl skeleton.
  • the present invention also includes the above-described adhesive composition or anisotropic conductive adhesive composition, and circuit members having circuit electrodes are electrically connected to each other.
  • the circuit connection material used for bonding is provided.
  • the present invention also includes a first circuit member having a first circuit electrode formed on the main surface of the first circuit board, and a second circuit electrode formed on the main surface of the second circuit board.
  • a second circuit member disposed so that the second circuit electrode and the first circuit electrode face each other; and the first circuit member provided between the first circuit member and the second circuit member.
  • a connection member that electrically connects the second circuit member, and the connection member is a cured product of the adhesive composition or the anisotropic conductive adhesive composition of the present invention.
  • one of the first circuit board and the second circuit board is a glass substrate.
  • connection member that electrically connects the first circuit member and the second circuit member is a cured product of the adhesive composition or anisotropic conductive adhesive composition of the present invention. Therefore, sufficient adhesive strength and connection reliability are maintained, and peeling of the adhesive is sufficiently suppressed under high temperature and high humidity conditions.
  • the present invention although it is a radical curable adhesive, sufficient adhesive strength and connection reliability are maintained even at low temperature (for example, 140 ° C. or lower) and for a short time (for example, 5 seconds or shorter).
  • An adhesive composition capable of suppressing peeling from an adherend under high temperature and high humidity conditions can be provided.
  • (meth) acrylic acid means acrylic acid or methacrylic acid corresponding to it.
  • the adhesive composition according to this embodiment contains (a) a thermoplastic resin, (b) a radical polymerizable compound, (c) a radical polymerization initiator, and (d) an epoxy resin having no (meth) acryloyloxy group. To do.
  • the adhesive composition does not substantially contain an epoxy resin cationic polymerization curing agent.
  • the fact that the cation polymerization curing agent of the epoxy resin is not substantially contained means that the content of the cation polymerization curing agent of the epoxy resin is 1 with respect to 100 parts by mass of the total amount of the component (a) and the component (b). Although it is less than 5 parts by mass, it is preferably less than 1.0 part by mass, more preferably less than 0.5 part by mass, and it does not contain an epoxy resin cationic polymerization curing agent. preferable.
  • An epoxy resin cationic polymerization curing agent is a Bronsted acid, a Lewis acid, and a compound capable of generating these acids by energy such as heat and light.
  • Examples of the cationic polymerization curing agent for the epoxy resin include onium salts.
  • thermoplastic resin (a) examples include one or more selected from polyimide resin, polyamide resin, phenoxy resin, poly (meth) acrylic resin, polyester resin, polyurethane resin, polyester urethane resin, and polyvinyl butyral resin. These resins are mentioned.
  • the lower limit of the weight average molecular weight of the thermoplastic resin may be 5000 or more, or 10,000 or more. There exists a tendency for the adhesive strength of an adhesive composition to improve that the weight average molecular weight of a thermoplastic resin is 5000 or more.
  • the upper limit of the weight average molecular weight of the thermoplastic resin may be 400000 or less, 200000 or less, or 150,000 or less. If the weight average molecular weight of the thermoplastic resin is 400000 or less, good compatibility with other components tends to be easily obtained, and the fluidity of the adhesive tends to be easily obtained.
  • the weight average molecular weight of the thermoplastic resin is preferably from 5,000 to 400,000, more preferably from 5,000 to 200,000, particularly preferably from 10,000 to 150,000.
  • thermoplastic resin a rubber component can also be used for the purpose of stress relaxation and adhesion improvement.
  • the content of the thermoplastic resin is preferably 20 to 80 parts by mass, more preferably 30 to 70 parts by mass with respect to 100 parts by mass of the total amount of the components (a) and (b). More preferably, it is ⁇ 65 parts by mass. If the content of the thermoplastic resin is 20 parts by mass or more, the adhesive strength tends to be improved or the film formability of the adhesive composition tends to be improved, and if it is 80 parts by mass or less, the adhesive It tends to be easy to obtain fluidity.
  • the adhesive composition according to the present embodiment may contain any (b) radical polymerizable compound.
  • the radical polymerizable compound may be, for example, any of the monomer and oligomer of the compound described later, or may be a combination of both.
  • one or more polyfunctional (meth) acrylate compounds having two or more (meth) acryloyloxy groups are preferable.
  • examples of such (meth) acrylate compounds include epoxy (meth) acrylate, urethane (meth) acrylate, polyether (meth) acrylate, polyester (meth) acrylate, trimethylolpropane tri (meth) acrylate, and polyethylene glycol diester.
  • Polyalkylene glycol di (meth) acrylate such as (meth) acrylate, dicyclopentenyl (meth) acrylate, dicyclopentenyloxyethyl (meth) acrylate, neopentyl glycol di (meth) acrylate, dipentaerythritol hexa (meth) Examples include acrylate, isocyanuric acid-modified bifunctional (meth) acrylate, and isocyanuric acid-modified trifunctional (meth) acrylate.
  • Examples of the epoxy (meth) acrylate include, for example, an epoxy (meth) acrylate obtained by adding (meth) acrylic acid to two glycidyl groups of bisphenol fluorenediglycidyl ether and ethylene glycol in two glycidyl groups of bisphenol fluorenediglycidyl ether. And / or the compound which introduce
  • the adhesive composition may contain a monofunctional (meth) acrylate compound as the (b) radical polymerizable compound for the purpose of controlling fluidity.
  • monofunctional (meth) acrylate compounds include pentaerythritol (meth) acrylate, 2-cyanoethyl (meth) acrylate, cyclohexyl (meth) acrylate, dicyclopentenyl (meth) acrylate, and dicyclopentenyloxyethyl (meth).
  • the adhesive composition contains a compound having a radical polymerizable functional group such as an allyl group, a maleimide group, and a vinyl group as the (b) radical polymerizable compound for the purpose of improving the crosslinking rate. Also good.
  • the adhesive composition preferably contains a radical polymerizable compound having a phosphate group as the (b) radical polymerizable compound for the purpose of improving the adhesive strength.
  • a radical polymerizable compound having a phosphate group as the (b) radical polymerizable compound for the purpose of improving the adhesive strength.
  • examples of the radically polymerizable compound having a phosphoric acid group include compounds represented by the following formula (1), (2) or (3).
  • R 5 represents a hydrogen atom or a methyl group
  • R 6 represents a (meth) acryloyloxy group
  • w and x each independently represents an integer of 1 to 8.
  • a plurality of R 5 , R 6 , w and x in the same molecule may be the same or different.
  • R 7 represents a (meth) acryloyloxy group
  • y and z each independently represents an integer of 1 to 8.
  • a plurality of R 7 , y and z in the same molecule may be the same or different.
  • R 8 represents a hydrogen atom or a methyl group
  • R 9 represents a (meth) acryloyloxy group
  • b and c each independently represent an integer of 1 to 8.
  • a plurality of R 8 and b in the same molecule may be the same or different.
  • radical polymerizable compound having a phosphoric acid group examples include acid phosphooxyethyl (meth) acrylate, acid phosphooxypropyl (meth) acrylate, acid phosphooxypolyoxyethylene glycol mono (meth) acrylate, and acid phosphooxypolyoxy.
  • Propylene glycol mono (meth) acrylate, 2,2'-di (meth) acryloyloxydiethyl phosphate, EO (ethylene oxide) modified di (meth) acrylate, phosphoric acid modified epoxy (meth) acrylate and vinyl phosphate Can be mentioned. These compounds can be used individually by 1 type or in combination of 2 or more types.
  • the content of the radically polymerizable compound having a phosphoric acid group is preferably 0.1 to 15 parts by mass with respect to 100 parts by mass of the total amount of the components (a) and (b), and 0.5 to 10 More preferably, it is more preferably 1 to 5 parts by mass. If the content of the radically polymerizable compound having a phosphoric acid group is 0.1 parts by mass or more, high adhesive strength tends to be obtained, and if it is 15 parts by mass or less, It is difficult to cause deterioration in physical properties, and the effect of improving reliability is good.
  • the total content of the (b) radical polymerizable compound contained in the adhesive composition is preferably 20 to 80 parts by mass with respect to 100 parts by mass of the total amount of the components (a) and (b). More preferably, it is ⁇ 70 parts by mass, and still more preferably 35-65 parts by mass. If the total content is 20 parts by mass or more, the heat resistance tends to be improved, and if it is 80 parts by mass or less, the effect of suppressing peeling after leaving in a high temperature and high humidity environment tends to increase.
  • the radical polymerization initiator can be arbitrarily selected from compounds such as peroxides and azo compounds. From the viewpoint of stability, reactivity, and compatibility, a peroxide having a one-minute half-life temperature of 90 to 175 ° C. and a molecular weight of 180 to 1000 is preferred. “1 minute half-life temperature” refers to a temperature at which the half-life of the peroxide is 1 minute. “Half-life” refers to the time taken for the concentration of a compound to decrease to half of its initial value at a given temperature.
  • radical polymerization initiator examples include 1,1,3,3-tetramethylbutylperoxyneodecanoate, di (4-tert-butylcyclohexyl) peroxydicarbonate, di (2-ethylhexyl) peroxydi Carbonate, cumylperoxyneodecanoate, 1,1,3,3-tetramethylbutylperoxyneodecanoate, dilauroyl peroxide, 1-cyclohexyl-1-methylethylperoxyneodecanoate, t- Hexyl peroxyneodecanoate, t-butyl peroxyneodecanoate, t-butyl peroxypivalate, 1,1,3,3-tetramethylbutylperoxy-2-ethylhexanoate, 2,5 -Dimethyl-2,5-di (2-ethylhexanoylperoxy) hexane, t-hexyl
  • the content of the radical polymerization initiator is preferably 1 to 15 parts by mass and more preferably 2.5 to 10 parts by mass with respect to 100 parts by mass of the total amount of the components (a) and (b).
  • the amount is preferably 3 to 8 parts by mass.
  • Examples of the epoxy resin having no (meth) acryloyloxy group include bisphenol A type epoxy resin, bisphenol F type epoxy resin, bisphenol S type epoxy resin, phenol novolac type epoxy resin, cresol novolac type epoxy resin, and bisphenol.
  • an aromatic polycyclic epoxy resin and an epoxy resin having a biphenyl skeleton are preferable, and an epoxy resin having a biphenyl skeleton is more preferable.
  • These can be used individually by 1 type or in combination of 2 or more types.
  • the lower limit of the molecular weight of the epoxy resin having no (meth) acryloyloxy group may be 250 or more, 300 or more, or 350 or more.
  • the upper limit of the molecular weight of the epoxy resin having no (meth) acryloyloxy group may be 5000 or less, 3000 or less, or 1000 or less.
  • the molecular weight of the epoxy resin having no (meth) acryloyloxy group is preferably 250 to 5000, more preferably 300 to 3000, and further preferably 350 to 1000.
  • the lower limit value of the epoxy equivalent of the epoxy resin having no (meth) acryloyloxy group may be 100 or more, 150 or more, or 180 or more. If the epoxy equivalent is 100 or more, the connection reliability of the adhesive composition tends to be further improved.
  • the upper limit of the epoxy equivalent of an epoxy resin having no (meth) acryloyloxy group may be 300 or less, 275 or less, or 270 or less. There exists a tendency for the adhesiveness with respect to glass to increase that an epoxy equivalent is 300 or less. From the above viewpoint, the epoxy equivalent of the epoxy resin having no (meth) acryloyloxy group is preferably 100 to 300, more preferably 150 to 275, and still more preferably 180 to 270.
  • the lower limit of the content of the epoxy resin having no (meth) acryloyloxy group may be 1 part by mass or more with respect to 100 parts by mass of the total amount of the components (a) and (b), and 2.5 masses. Or 3 parts by mass or more. If the content is 1 part by mass or more, the effect of the present invention tends to be easily obtained at a higher level.
  • the upper limit of the content of the epoxy resin having no (meth) acryloyloxy group may be 15 parts by mass or less with respect to 100 parts by mass of the total amount of the component (a) and the component (b), and 10 masses. Or less. When the content is 15 parts by mass or less, radical polymerization tends to be difficult to inhibit when used under low temperature and short time conditions.
  • the content of the epoxy resin having no (meth) acryloyloxy group is preferably 1 to 15 parts by mass with respect to 100 parts by mass as the total of the components (a) and (b). More preferably, it is 5 to 10 parts by mass, and further preferably 3 to 10 parts by mass.
  • the adhesive composition according to this embodiment may contain a silane coupling agent.
  • the silane coupling agent is preferably a compound represented by the following formula (4).
  • R 1 , R 2 and R 3 are each independently a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, an alkoxy group having 1 to 5 carbon atoms, an alkoxycarbonyl group having 1 to 5 carbon atoms or An aryl group is shown. At least one of R 1 , R 2 and R 3 is an alkoxy group.
  • R 4 is a (meth) acryloyl group, a (meth) acryloyloxy group, a vinyl group, an isocyanate group, an imidazole group, a mercapto group, an amino group optionally substituted with an aminoalkyl group, a methylamino group, a dimethylamino group, A benzylamino group, a phenylamino group, a cyclohexylamino group, a morpholino group, a piperazino group, a ureido group, a glycidyl group or a glycidoxy group; a represents an integer of 0 to 10.
  • silane coupling agent of the formula (4) examples include vinyltrimethoxysilane, vinyltriethoxysilane, 3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropylmethyldiethoxysilane, 3- (meth) Acryloxypropylmethyldimethoxysilane, 3- (meth) acryloxypropyltrimethoxysilane, 3- (meth) acryloxypropylmethyldiethoxysilane, 3- (meth) acryloxypropyltriethoxysilane, N-2- (amino Ethyl) -3-aminopropylmethyldimethoxysilane, N-phenyl-3-aminopropyltrimethoxysilane, 3-ureidopropyltriethoxysilane, 3-mercaptopropyltrimethoxysilane and 3-isocyanatopropyltriethoxysilane. That. These compounds can be used individually by 1 type or in combination of
  • the content of the silane coupling agent is preferably 0.1 to 10 parts by mass and preferably 0.25 to 5 parts by mass with respect to 100 parts by mass of the total amount of the components (a) and (b). Is more preferable. If the content of the silane coupling agent is 0.1 parts by mass or more, the effect of suppressing the separation of the interface between the circuit member and the circuit connecting material and the generation of bubbles tends to increase. When the content is 10 parts by mass or less, the pot life of the adhesive composition tends to be long.
  • a silane coupling agent has radically polymerizable functional groups, such as an acryloyl group (acryloyloxy group), it shall be contained in (b) component as a radically polymerizable compound.
  • the adhesive composition according to this embodiment may further contain (e) conductive particles.
  • the adhesive composition containing conductive particles can be particularly suitably used as an anisotropic conductive adhesive composition.
  • the conductive particles include metal particles such as Au, Ag, Pd, Ni, Cu, and solder, and carbon particles.
  • the conductive particles are composite particles having core particles made of a non-conductive material such as glass, ceramic, and plastic, and conductive layers such as metal, metal particles, and carbon that coat the core particles. May be.
  • the metal particles may be copper particles and particles having a silver layer covering the copper particles.
  • the core particle of the composite particle is preferably a plastic particle.
  • the composite particles having the plastic particles as the core particles have a deformability that is deformed by heating and pressurization. Therefore, when the circuit members are bonded to each other, the contact area between the circuit electrodes of the circuit members and the conductive particles Can be increased. Therefore, according to the adhesive composition containing these composite particles as conductive particles, a connection body that is more excellent in terms of connection reliability can be obtained.
  • the adhesive composition may contain insulating coated conductive particles having the conductive particles and an insulating layer or insulating particles covering at least a part of the surface of the conductive particles.
  • the insulating layer can be provided by a method such as hybridization.
  • the insulating layer or the insulating particles are formed from an insulating material such as a polymer resin.
  • the average particle diameter of the conductive particles is preferably 1 to 18 ⁇ m from the viewpoint of obtaining good dispersibility and conductivity.
  • the content of the conductive particles is preferably 0.1 to 30% by volume, more preferably 0.1 to 10% by volume, based on the total volume of the adhesive composition, and 0.5 to More preferably, it is 7.5 volume%. If content of electroconductive particle is 0.1 volume% or more, there exists a tendency for electroconductivity to improve. There exists a tendency for it to become difficult to produce the short circuit between circuit electrodes as content of electroconductive particle is 30 volume% or less. Content (volume%) of electroconductive particle is determined based on the volume in 23 degreeC of each component which comprises the adhesive composition before hardening. The volume of each component can be determined by converting mass to volume using specific gravity. Put an appropriate solvent (water, alcohol, etc.) that can wet the component well without dissolving or swelling the component whose volume is to be measured. The increased volume can be obtained as the volume of the component.
  • an appropriate solvent water, alcohol, etc.
  • the adhesive composition may contain insulating organic or inorganic fine particles in addition to the conductive particles.
  • the inorganic fine particles include metal fine particles such as silica fine particles, alumina fine particles, silica-alumina fine particles, titania fine particles, zirconia fine particles, and nitride fine particles.
  • the organic fine particles include silicone fine particles, methacrylate-butadiene-styrene fine particles, acryl-silicone fine particles, polyamide fine particles, and polyimide fine particles. These fine particles may have a uniform structure or a core-shell type structure.
  • the content of the organic fine particles and the inorganic fine particles is preferably 5 to 30 parts by mass, and preferably 7.5 to 20 parts by mass with respect to 100 parts by mass of the total amount of the components (a) and (b). More preferred. If the content of the organic fine particles and the inorganic fine particles is 5 parts by mass or more, it tends to be relatively easy to maintain the electrical connection between the opposing electrodes, and if it is 30 parts by mass or less, the adhesive composition There is a tendency for the fluidity of things to improve.
  • the adhesive composition may contain various additives.
  • the adhesive composition according to the present embodiment can be used as a paste adhesive when it is liquid at normal temperature (25 ° C.). When the adhesive composition is solid at normal temperature, it may be used by heating, or it may be used by pasting it by adding a solvent.
  • the solvent used for pasting is not particularly limited as long as it has substantially no reactivity with the adhesive composition (including additives) and can sufficiently dissolve the adhesive composition. Not.
  • the adhesive composition according to the present embodiment can be formed into a film and used as a film adhesive.
  • a film adhesive is obtained by applying a solution obtained by adding a solvent or the like to an adhesive composition as necessary on a peelable support such as a fluororesin film, a polyethylene terephthalate film, or a release paper. It can be obtained by a method of removing a solvent or the like.
  • a film adhesive is more convenient in terms of handling and the like.
  • FIG. 1 is a schematic cross-sectional view showing an embodiment of a film adhesive comprising the adhesive composition according to the present embodiment.
  • a laminated film 100 shown in FIG. 1 includes a support 8 and a film adhesive 40 laminated on the support 8 in a peelable manner.
  • the film adhesive 40 is composed of an insulating adhesive layer 5 and conductive particles 7 dispersed in the insulating adhesive layer 5.
  • the insulating adhesive layer 5 is comprised from components other than electroconductive particle among the above-mentioned adhesive compositions. According to this film adhesive, it is easy to handle, can be easily installed on the adherend, and can be easily connected.
  • the film adhesive may have a multilayer structure composed of two or more layers. When the film adhesive contains conductive particles, the film adhesive can be suitably used as an anisotropic conductive film.
  • the adherends can usually be bonded together using heating and pressurization together.
  • the heating temperature is preferably 100 to 250 ° C.
  • the pressure is not particularly limited as long as it does not damage the adherend, but it is generally preferably 0.1 to 10 MPa. These heating and pressurization are preferably performed in the range of 0.5 to 120 seconds.
  • the adherends are sufficiently bonded to each other even when heated and pressed for a short time of 5 seconds under conditions of 140 ° C. and 1 MPa. It is possible.
  • the adhesive composition and film adhesive according to this embodiment can be used as an adhesive for different types of adherends having different thermal expansion coefficients.
  • the adhesive composition and the film-like adhesive according to the present embodiment include an anisotropic conductive adhesive, a circuit connecting material such as a silver paste and a silver film, an elastomer for CSP, an underfill material for CSP, It can be used as a semiconductor element adhesive material such as LOC tape.
  • the circuit connection material according to the present embodiment contains the above-described adhesive composition or anisotropic conductive adhesive composition.
  • Such a circuit connection material can be used for bonding circuit members having circuit electrodes so that the circuit electrodes of the respective circuit members are electrically connected to each other.
  • connection body using the film adhesive according to the present embodiment as an anisotropic conductive film, connecting circuit members having circuit electrodes formed on the main surface of the circuit board and the circuit board as adherends, An example of manufacturing the connection body will be described.
  • FIG. 2 is a schematic cross-sectional view showing an embodiment of a connection body including a connection member made of a cured product of the adhesive composition according to this embodiment.
  • the connection body 1 shown in FIG. 2 includes a first circuit member 20 and a second circuit member 30 that are arranged to face each other.
  • a connecting member 10 is provided between the first circuit member 20 and the second circuit member 30 to bond and connect them.
  • the first circuit member 20 includes a first circuit board 21 and a first circuit electrode 22 formed on the main surface 21 a of the first circuit board 21.
  • An insulating layer may be formed on the main surface 21 a of the first circuit board 21.
  • the second circuit member 30 includes a second circuit board 31 and a second circuit electrode 32 formed on the main surface 31 a of the second circuit board 31.
  • An insulating layer may also be formed on the main surface 31 a of the second circuit board 31.
  • the first circuit member 20 and the second circuit member 30 are not particularly limited as long as they have circuit electrodes that require electrical connection.
  • a substrate made of an inorganic material such as a semiconductor, glass or ceramic
  • a substrate made of an organic material such as polyimide or polycarbonate
  • an inorganic material such as glass / epoxy
  • an organic material such as polyimide or polycarbonate
  • an inorganic material such as glass / epoxy
  • an organic material are used.
  • the first circuit board 21 may be a glass substrate
  • the second circuit board 31 may be a flexible substrate (preferably a resin film such as a polyimide film).
  • circuit members to be connected include glass or plastic substrates, printed wiring boards, ceramic wiring boards, flexible wiring boards on which electrodes such as ITO (indium tin oxide) films are formed, which are used in liquid crystal displays. And a semiconductor silicon chip. These are used in combination as necessary.
  • a member having a surface formed from an organic material such as a printed wiring board and a polyimide film
  • a metal such as copper or aluminum, ITO, silicon nitride
  • connection body obtained by connecting them is a solar cell, It is a solar cell module provided with a tab wire and a connecting member (cured product of the adhesive composition) for bonding them.
  • the connecting member 10 is made of a cured product of the adhesive composition according to the present embodiment.
  • the connecting member 10 contains an insulating layer 11 and conductive particles 7 dispersed in the insulating layer 11.
  • the electroconductive particle 7 is arrange
  • the connection member does not contain conductive particles, the first circuit electrode 22 and the second circuit electrode 32 come into contact with each other to be electrically connected.
  • connection member 10 is formed of a cured product of the adhesive composition according to this embodiment, the bonding strength of the connection member 10 to the first circuit member 20 and the second circuit member 30 is sufficiently high. Therefore, even after a reliability test (high temperature and high humidity test), it is possible to sufficiently suppress a decrease in adhesive strength and an increase in connection resistance.
  • connection body 1 includes, for example, a step of disposing a pair of circuit members having circuit electrodes disposed opposite to each other with a film adhesive made of an adhesive composition interposed therebetween, a pair of circuit members, and a film adhesive A step of bonding a pair of circuit members via a cured product of the adhesive composition (main connection step) by heating and curing the agent while pressing in the thickness direction of the film adhesive. Can be manufactured.
  • FIG. 3 is a process diagram showing a schematic cross-sectional view of one embodiment for producing a connection body using the adhesive composition according to the present embodiment.
  • the film adhesive 40 is placed on the main surface of the first circuit member 20 on the first circuit electrode 22 side.
  • the laminate of the film adhesive and the support is a circuit member in such a direction that the film adhesive 40 is positioned on the first circuit member 20 side. It is put on.
  • the film adhesive 40 is easy to handle because it is in the form of a film. For this reason, the film adhesive 40 can be easily interposed between the first circuit member 20 and the second circuit member 30, and the connection between the first circuit member 20 and the second circuit member 30 is possible. Work can be done easily.
  • the film adhesive 40 is the above-described adhesive composition (circuit connection material) formed in a film shape, and includes the conductive particles 7 and the insulating adhesive layer 5. Even when the adhesive composition does not contain conductive particles, it can be used as a circuit connection material for electrical connection by directly connecting the circuit electrodes.
  • the circuit connection material that does not contain conductive particles is sometimes called NCF (Non-Conductive-FILM) or NCP (Non-Conductive-Paste).
  • NCF Non-Conductive-FILM
  • NCP Non-Conductive-Paste
  • ACF isotropic Conductive FILM
  • ACP Analogenotropic Conductive Paste
  • the thickness of the film adhesive 40 is preferably 10 to 50 ⁇ m. If the thickness of the film adhesive 40 is 10 ⁇ m or more, the space between the first circuit electrode 22 and the second circuit electrode 32 tends to be easily filled with the adhesive. If the thickness of the film adhesive is 50 ⁇ m or less, the adhesive composition between the first circuit electrode 22 and the second circuit electrode 32 can be sufficiently eliminated, and the first circuit electrode 22 and the second circuit electrode The conduction between the two circuit electrodes 32 can be easily ensured.
  • the film adhesive 40 is temporarily connected to the first circuit member 20 (FIG. 3). (See (b) of). At this time, you may pressurize, heating. However, the heating temperature is set to a temperature sufficiently lower than the temperature at which the adhesive composition in the film adhesive 40 is not cured, that is, the temperature at which the radical polymerization initiator rapidly generates radicals.
  • the second circuit member 30 is placed on the film adhesive 40 in such a direction that the second circuit electrode is positioned on the first circuit member 20 side.
  • the second circuit member 30 is placed on the film adhesive 40 after the support is peeled off.
  • the film adhesive 40 is heated while applying pressures A and B in the thickness direction.
  • the heating temperature at this time is set to a temperature at which the radical polymerization initiator sufficiently generates radicals.
  • radicals are generated from the radical polymerization initiator, and polymerization of the radical polymerizable compound is started.
  • the connection shown in FIG. 2 is obtained by this connection.
  • the insulating adhesive is cured to form the insulating layer 11 in a state where the distance between the first circuit electrode 22 and the second circuit electrode 32 is sufficiently small. .
  • the first circuit member 20 and the second circuit member 30 are firmly connected via the connection member 10 including the insulating layer 11.
  • connection is preferably performed under the conditions of a heating temperature of 100 to 250 ° C., a pressure of 0.1 to 10 MPa, and a pressurization time of 0.5 to 120 seconds. These conditions are appropriately selected depending on the intended use, the adhesive composition, and the circuit member. According to the adhesive composition according to this embodiment, a connection body having sufficient reliability can be obtained even under a low temperature condition such as 140 ° C. or lower. After the connection, post-curing may be performed as necessary.
  • the reaction was continued for 15 hours after completion of the dropping, and when the NCO content was confirmed to be 0.2% by mass using an automatic potentiometric titrator (trade name AT-510, manufactured by Kyoto Electronics Industry Co., Ltd.) And urethane acrylate was obtained.
  • an automatic potentiometric titrator trade name AT-510, manufactured by Kyoto Electronics Industry Co., Ltd.
  • urethane acrylate was obtained.
  • the weight average molecular weight of urethane acrylate was 8500 (standard polystyrene conversion value).
  • the analysis by GPC was performed under the same conditions as the analysis of the weight average molecular weight of the polyurethane resin described above.
  • the reaction solution was returned to room temperature, and 300 parts by mass of benzene was added to dissolve the product. Subsequently, an aqueous sodium carbonate solution and distilled water were added thereto in this order, and the solution was washed three times. Thereafter, benzene was sufficiently distilled off to obtain a crude product.
  • a crude product was analyzed by liquid phase chromatography, in addition to the acrylate compound having one epoxy group as the target compound, a bifunctional acrylate compound having no epoxy group and the raw material bisphenol F type epoxy resin were crude products. It was found to be included. Therefore, the crude product was purified to obtain acrylate compound A having an epoxy group and an acryloyloxy group one by one and a bisphenol F type basic skeleton.
  • a flexible circuit board having 2200 copper circuits having a line width of 75 ⁇ m, a pitch of 150 ⁇ m and a thickness of 18 ⁇ m, a glass substrate and a thickness of 0 formed on the glass substrate
  • An ITO substrate (thickness 1.1 mm, surface resistance 20 ⁇ / ⁇ ) having a thin layer of 2 ⁇ m indium oxide (ITO) was connected.
  • the connection was made by heating and pressurizing at 140 ° C. and 1 MPa for 5 seconds using a thermocompression bonding apparatus (heating method: constant heat type, manufactured by Toray Engineering Co., Ltd.).
  • a connection body in which the FPC and the ITO substrate were connected by a cured product of a film adhesive over a width of 1.5 mm was produced.
  • a SiN substrate (thickness 0.7 mm) having a glass substrate and a thin layer of 0.2 ⁇ m silicon nitride (SiN) formed on the glass substrate is used at 140 ° C. and 3 MPa.
  • a connection body between the FPC and the SiN substrate was produced by heating and pressurizing for 5 seconds.
  • connection resistance connection resistance
  • adhesive strength was measured by a 90-degree peeling method according to JIS-Z0237.
  • Tensilon UTM-4 manufactured by Toyo Baldwin Co., Ltd., trade name, peel strength 50 mm / min, 25 ° C. was used as an adhesive strength measuring device.
  • the connection resistance and the adhesive strength were measured for the connection body immediately after the connection and after being kept in a constant temperature and humidity chamber at 85 ° C. and 85% RH for 250 hours. The evaluation results are shown in Table 3.
  • connection resistance 5 ⁇ or less
  • adhesive strength 8 N / cm
  • Comparative Example 1 containing no epoxy resin and Comparative Example 2 containing 1 part by mass or more of the cationic polymerization curing agent of epoxy resin, the adhesive strength after the high-temperature and high-humidity test is sufficient as compared with each Example. Furthermore, when a SiN substrate was used, the occurrence of peeling was observed after the high-temperature and high-humidity test, and practical problems were also observed in the connection appearance.
  • SYMBOLS 1 Connection body, 5 ... Insulating adhesive layer, 7 ... Conductive particle, 8 ... Support body, 10 ... Connection member, 11 ... Insulating layer, 20 ... First circuit member, 21 ... First circuit board, 21a ... main surface, 22 ... first circuit electrode, 30 ... second circuit member, 31 ... second circuit board, 31a ... main surface, 32 ... second circuit electrode, 40 ... film adhesive, 100 ... Laminated film.

Abstract

La présente invention concerne une composition adhésive qui comprend (a) une résine thermoplastique, (b) un composé polymérisable par voie radicalaire, (c) un initiateur de polymérisation radicalaire, et (d) une résine époxy ne contenant pas de groupe (méth)acryloyloxy et qui ne contient sensiblement pas de durcisseur de polymérisation cationique pour la résine époxy.
PCT/JP2015/075253 2015-09-04 2015-09-04 Composition adhésive, composition adhésive électroconductrice de façon anisotrope, matériau de connexion de circuit, et objet connecté WO2017037951A1 (fr)

Priority Applications (4)

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PCT/JP2015/075253 WO2017037951A1 (fr) 2015-09-04 2015-09-04 Composition adhésive, composition adhésive électroconductrice de façon anisotrope, matériau de connexion de circuit, et objet connecté
CN201580082812.8A CN107922817B (zh) 2015-09-04 2015-09-04 粘接剂组合物、各向异性导电性粘接剂组合物、电路连接材料及连接体
KR1020187008753A KR102376223B1 (ko) 2015-09-04 2015-09-04 접착제 조성물, 이방 도전성 접착제 조성물, 회로 접속 재료 및 접속체
JP2017537184A JP6631631B2 (ja) 2015-09-04 2015-09-04 接着剤組成物、異方導電性接着剤組成物、回路接続材料及び接続体

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Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH10168412A (ja) * 1996-12-10 1998-06-23 Sumitomo Bakelite Co Ltd 異方導電性接着剤
JP2013138013A (ja) * 2009-11-16 2013-07-11 Hitachi Chemical Co Ltd 回路接続材料及びそれを用いた回路部材の接続構造
JP2015183118A (ja) * 2014-03-25 2015-10-22 日立化成株式会社 接着剤組成物、異方導電性接着剤組成物、回路接続材料及び接続体

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2610900B2 (ja) 1987-10-27 1997-05-14 ソニーケミカル 株式会社 熱硬化型異方性導電接着シート及びその製造方法
TWI229119B (en) 1997-03-31 2005-03-11 Hitachi Chemical Co Ltd Circuit-connecting material and circuit terminal connected structure and connecting method
US6225408B1 (en) * 1998-06-12 2001-05-01 Lord Corporation Adhesive formulations
JP5867508B2 (ja) 2011-09-06 2016-02-24 日立化成株式会社 回路接続材料及び接続体

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH10168412A (ja) * 1996-12-10 1998-06-23 Sumitomo Bakelite Co Ltd 異方導電性接着剤
JP2013138013A (ja) * 2009-11-16 2013-07-11 Hitachi Chemical Co Ltd 回路接続材料及びそれを用いた回路部材の接続構造
JP2015183118A (ja) * 2014-03-25 2015-10-22 日立化成株式会社 接着剤組成物、異方導電性接着剤組成物、回路接続材料及び接続体

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KR102376223B1 (ko) 2022-03-17
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CN107922817B (zh) 2021-05-28
JPWO2017037951A1 (ja) 2018-07-26
JP6631631B2 (ja) 2020-01-15

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