JP2008156570A - Method of manufacturing latent hardening agent particle, method of manufacturing adhesive, and method of manufacturing adhesive film - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide latent hardening agent particles high in storing stability and also high in hardening property. <P>SOLUTION: In the invention, the content of a main hardening agent of the latent hardening agent particle is increased by impregnating resin particles with the main hardening agent, and an adhesive is hardened at a low temperature. The latent hardening agent particles having undecomposed main hardening agent can be prepared by impregnating the resin particles with the main hardening agent after manufacturing of the resin particles even if the main hardening agent is such an agent decomposing in a manufacturing process. The latent hardening agent particles containing both of an auxiliary hardening agent and the main hardening agent can be prepared by making an impregnating liquid contain the auxiliary hardening agent. In the latent hardening agent particle like this, the adhesive can be hardened even when the auxiliary hardening agent is not added into a binder of the adhesive. <P>COPYRIGHT: (C)2008,JPO&INPIT

Description

  The present invention relates to a method for producing an adhesive and a method for producing latent curing agent particles used in the adhesive.

Generally, a curing agent for curing a thermosetting resin is added to the adhesive, and latent curing agent particles encapsulating the curing agent are conventionally used to improve the storage stability of the adhesive.
As latent curing agent particles, for example, those in which a curing agent such as aluminum chelate is held in polyurea resin particles are known (see, for example, Patent Document 3).

However, since the polyurea resin particles are easily penetrated into the particles by the organic solvent in the adhesive and the low molecular thermosetting resin, when using the latent curing agent particles, the type and amount of the organic solvent, There were limitations on the type of thermosetting resin.
In addition, since the polyurea resin particles have high thermal responsiveness, the polyurea resin particles are efficient when thermally curing the adhesive, but there is also a problem that a large amount of the curing agent cannot be retained.
JP-A-6-238158 JP-A-8-131816 International Publication No. 2005/033173 Pamphlet JP 2004-246231 A JP 2005-114325 A

  The present invention has been made to solve the above-mentioned problems, and its purpose is to provide latent curing agent particles and an adhesive that are highly reactive when curing an adhesive and have excellent storage stability. is there.

In order to solve the above problems, the present invention is a latent curing agent particle to be dispersed in an adhesive, wherein the reaction product with an auxiliary curing agent contains a main curing agent that cures the adhesive. A method for producing latent curing agent particles for producing curing agent particles, a raw material liquid production step for producing a raw material liquid having a reactive resin capable of polymerization reaction and the main curing agent, and heating the raw material liquid A resin particle production step of polymerizing the reactive resin to produce resin particles containing the main curing agent, and bringing the resin particles into contact with an impregnating liquid to which the main curing agent is added. A method for producing latent curing agent particles, comprising impregnating the resin particles with a curing agent and increasing the content of the main curing agent in the resin particles.
The present invention is a method for producing latent curing agent particles, wherein the auxiliary curing agent is a substance that inhibits polymerization of the reactive resin, and the impregnating liquid contains latent auxiliary curing agent particles. It is a manufacturing method.
The present invention is a method for producing latent curing agent particles, wherein the raw material liquid production step includes a dispersion step in which the reactive resin and the main curing agent are dispersed in a main solvent that decomposes the main curing agent. This is a method for producing a conductive curing agent particle.
The present invention is a method for producing latent curing agent particles, wherein the reactive resin is a reactive monomer that can be polymerized by reacting with the main solvent, and a thermally polymerizable monomer that forms droplets in the main solvent. The latent curing agent particles are dispersed in the main solvent together with the main curing agent.
The present invention is a method for producing latent curing agent particles, wherein the auxiliary curing agent is a method for producing latent curing agent particles that inhibits a polymerization reaction of the reactive monomer.
This invention is a manufacturing method of latent hardener particle | grains, Comprising: It is a manufacturing method of latent hardener particle | grains using what has water as a main component as said main solvent.
The present invention is a method for producing latent curing agent particles, wherein the reactive monomer is an isocyanate.
This invention is a manufacturing method of latent hardener particle | grains, Comprising: The said thermopolymerizable monomer is a manufacturing method of latent hardener particle | grains which are any one or both of a vinyl monomer and an acrylic monomer.
The present invention is a method for producing latent curing agent particles, wherein the main curing agent is a metal chelate and the auxiliary curing agent is a silane compound.
The present invention is a method for producing latent curing agent particles, wherein the latent curing agent particles are immersed in a cleaning solution that dissolves the main curing agent and does not penetrate into the resin particles. It is a manufacturing method of the latent hardener particle | grains provided after the process.
The present invention is a method for producing latent curing agent particles, wherein the polymer of the reactive monomer is a polar resin, and the cleaning liquid is a nonpolar solvent.
The present invention is a method for producing latent curing agent particles, wherein the polymer of the reactive monomer is a polyurea resin, and the cleaning liquid is one kind selected from the group consisting of cyclohexane, hexane, and toluene. This is a method for producing latent curing agent particles containing the above polar solvent.
The present invention is a method for producing an adhesive, wherein the latent curing agent particles are dispersed in a binder containing a resin and an organic solvent.
The present invention is a method for producing an adhesive, wherein the binder contains the auxiliary curing agent.
This invention is a manufacturing method of an adhesive film, Comprising: After forming the coating layer of the said adhesive agent, the said organic solvent is removed from the said coating layer, and it is a manufacturing method of the adhesive film which makes the said coating layer into a film.

  In the present invention, the decrease in latency means that the latent curing agent particles are dissolved, swollen, or destroyed by heating or physical impact, so that the curing component contained in the latent curing agent particles is an adhesive. It becomes possible to come into contact with the component contained in the adhesive, and the curing reaction of the adhesive is started.

  The curing component in the latent particle is a main curing agent when only the main curing agent is contained in the latent curing agent particle, and both the main curing agent and the auxiliary curing agent are contained in the latent curing agent particle. When contained, they are a main curing agent, an auxiliary curing agent, and a reaction product of the main curing agent and the auxiliary curing agent.

  The present invention is configured as described above. A reactive resin (monomer) and a mixture of a main curing agent, or a reactive resin and a main curing agent are separately put in a main solvent, and the reactive resin and the main curing agent are mixed. The droplets of the raw material liquid having the above form droplets dispersed in the main solvent. When the reactive resin in the droplets is polymerized by heating, the droplets are cured to produce resin particles containing the main curing agent.

  If the main curing agent is a hydrolyzable material such as a metal chelate, create an impregnation solution in which the main curing agent is dissolved alone or in a solvent that does not contain water, and impregnate the resin particles with the impregnation solution. If the latent curing agent particles are prepared, the main curing agent is impregnated inside the resin particles without being hydrolyzed.

  Further, when the oil phase liquid is dispersed in the aqueous phase liquid in the production process of the resin particles, a part of the main curing agent in the oil phase liquid reacts with the water of the aqueous phase liquid and is hydrolyzed. Then, since the resin particles are impregnated with the main curing agent after the production process of the resin particles, the latent curing agent particles contain an unhydrolyzed main curing agent.

Since the main curing agent is held inside the resin particles, when the latent curing agent particles are added to the adhesive, the main curing agent comes into contact with the resin in the adhesive (for example, thermosetting resin) or moisture. Thus, not only does the adhesive not cure, but the main curing agent remains unhydrolyzed.
Therefore, the latent curing agent particles produced according to the present invention do not cure the adhesive during storage and reduce the potential of the unhydrolyzed main curing agent when heated during use.

  When the reaction product of the main curing agent and the auxiliary curing agent polymerizes the resin, the reaction product is not generated if the main curing agent is hydrolyzed, but the main curing agent inside the resin particles in the adhesive is not hydrolyzed. Since it is not decomposed, a reaction product with the auxiliary curing agent is generated, and the polymerization reaction of the resin proceeds.

  When the resin particles not containing the main curing agent are impregnated with the impregnating liquid, latent curing agent particles in which the main curing agent is held inside the resin particles are obtained. However, since it is difficult to contain a large amount of the main curing agent inside the resin particles only by impregnating the impregnating solution, in order to increase the content of the main curing agent, the resin particles are mainly used in the process of producing the resin particles. It is desirable to include a curing agent.

  Since the latent curing agent particles produced according to the present invention have a large content of the main curing agent, the effect speed when curing the adhesive is fast. The latent curing agent particles prepared using the impregnating liquid containing the auxiliary curing agent have an auxiliary curing agent in the inside thereof, and if such latent curing agent particles are used, the auxiliary curing agent is added to the adhesive. Since it is not necessary to add, the composition of the adhesive can be freely designed, and the properties such as tackiness can be controlled. If the latent curing agent particles impregnated with the impregnating liquid are washed, the main curing agent is removed from the surface, so that the storage stability of the adhesive when used as an adhesive is enhanced.

A process for producing an anisotropic conductive film by the production method of the present invention will be described.
In the case of producing an anisotropic conductive film, the latent curing agent particles for polymerizing the resin are dispersed in a liquid binder in which the resin is dissolved in an organic solvent and the conductive particles are dispersed, as described later. Create an adhesive.

The latent curing agent particles contain a main curing agent inside the resin particles, and even if an auxiliary curing agent that reacts with the main curing agent to polymerize the resin is added to the binder, it is latent curing at room temperature. Since the potential of the main curing agent in the agent particles does not decrease, the liquid adhesive does not cure.
A liquid adhesive is applied to the surface of the release film to form a coating layer, and then dried to evaporate and remove the organic solvent, whereby the coating layer becomes a film and an anisotropic conductive film is obtained.

When the coating layer is formed into a film, the concentration of the latent curing agent particles increases. However, as described above, the latent curing agent particles in the latent curing agent particles do not have a lower potential at room temperature. Does not cure.
When this anisotropically conductive film is heated during use, the latent curing agent in the latent curing agent particles has a reduced potential, and the primary curing agent and the auxiliary curing agent react to produce a reaction product. The resin in the binder is polymerized by the reaction product.

Next, the process of forming the latent curing agent particles will be described.
An oil obtained by mixing the main curing agent described above, a water-reactive monomer (reactive monomer) that decomposes upon contact with water, a lipophilic monomer (thermopolymerizable monomer) that polymerizes by heating, and a poorly water-soluble organic solvent. A phase liquid (raw material liquid) is prepared.
An aqueous phase liquid (main solvent) in which a dispersant and a surfactant are added to water is prepared, and the oil phase liquid is added to a larger amount of the aqueous phase liquid than the oil phase liquid and stirred.

  The main curing agent is a hydrolyzable substance, and when a large amount of the main curing agent is added to the oil phase liquid, the oil phase liquid gels due to the exothermic decomposition of the main curing agent. Hydrolysis is suppressed by the lipophilic monomer and the organic solvent in the phase liquid, and the oil phase liquid is not gelled but becomes droplets and is uniformly dispersed in the aqueous phase liquid.

  Since the water-reactive monomer is in contact with water on the surface of the droplet, the water-reactive monomer is hydrolyzed to produce an intermediate product, which reacts with the water-reactive monomer before hydrolysis. Then, a polymer of a water reactive monomer is generated on the surface of the droplet (interfacial polymerization).

When the suspension is heated, the lipophilic monomer is polymerized inside the droplet, and the polymerization of the water-reactive monomer is promoted, and the droplet is cured while the main curing agent is held inside.
At this time, if the heating temperature of the suspension is set to be higher than the boiling point of the organic solvent added to the oil phase liquid (for example, the heating temperature is 80 ° C. with respect to the boiling point of ethyl acetate of 77 ° C.), the organic solvent evaporates from the droplets. Resin particles are obtained which are composed of a polymer of water-reactive monomer which is removed and generated on the surface and a polymer of lipophilic monomer generated inside, and in which the main curing agent is retained.

In the interfacial polymerization method in which the droplets in the suspension are cured to form resin particles, the particle size of the droplets cannot be reduced if the oil phase liquid has poor dispersibility. Also grows. As described above, in the present application, since the oil phase liquid is uniformly dispersed in the aqueous phase liquid, the particle size of the resin particles can be reduced to a few μm unit.
Distilled water is added to the resin particles, washed and filtered to separate from the distilled water, and the aqueous liquid adhering to the surface is removed (pre-cleaning step).

Dissolve the main curing agent in a polar solvent that can dissolve the main curing agent to create an impregnation liquid, immerse the resin particles after removing the aqueous phase liquid in the impregnation liquid, and heat at a temperature at which the resin particles do not dissolve. Stir while stirring.
In the present invention, the water-reactive monomer is selected such that the polymer becomes a polar resin. For example, when the water-reactive monomer is isocyanate, the polymer is polyurea, and polyurea is a polar resin.

As described above, since the water-reactive monomer is on the surface portion of the resin particle, when the resin particle is immersed in the impregnating liquid, the main curing agent passes through the surface of the resin particle together with the polar solvent and enters the inside. The particles are swollen with the impregnation liquid.
Therefore, when the resin particles are separated from the impregnating liquid, latent curing agent particles in which a larger amount of the main curing agent is retained inside the resin particles than before being immersed in the impregnating liquid are obtained. In a state separated from the impregnating liquid, the impregnating liquid adheres to the surface of the latent curing agent resin particles.

If the concentration of the main curing agent in the impregnating liquid is high and the latent curing agent particles are added to the adhesive as they are, there is a risk that the resin in the binder will polymerize without heating, before adding to the adhesive, The latent curing agent particles are washed with a solvent capable of dissolving the main curing agent.
Specifically, when a nonpolar solvent capable of dissolving the main curing agent is prepared as a cleaning liquid, and the latent curing agent particles are immersed in the cleaning liquid, the main curing agent adhering to the resin particle surface of the latent curing agent particles is the cleaning liquid. Dissolved in and removed.

As described above, there is a polar resin on the surface of the resin particles, and the polar resin does not permeate the nonpolar solvent, so that the cleaning liquid does not permeate the resin particles. Therefore, the main curing agent inside the resin particles remains without being eluted in the cleaning liquid.
When the latent curing agent particles are filtered off from the cleaning liquid and dried, the cleaning liquid adhering to the surface of the resin particles and the polar solvent of the impregnating liquid impregnated inside the resin particles are removed by evaporation.

Since the latent curing agent particles after washing have the impregnating liquid removed from the surface of the resin particles as described above, no main curing agent remains on the surface of the resin particles, and the main curing agent is contained inside the resin particles. Only contained.
Therefore, when the latent curing agent particles after washing are added to the adhesive, the main curing agent does not come into contact with the auxiliary curing agent or the resin unless it is heated, so that the storage stability of the adhesive is further improved.

The above describes the case where the resin particles are impregnated with the impregnating liquid composed of the main curing agent and the polar solvent, but the present invention is not limited to this.
For example, when the auxiliary curing agent is a liquid and is a polar compound having a polar group in the chemical structure, the auxiliary curing agent is contained in the impregnation liquid instead of the polar solvent or together with the polar solvent. When the resin particles are immersed in the impregnating solution, the auxiliary curing agent enters the resin particles, and latent curing agent particles containing the main curing agent and the auxiliary curing agent are obtained.

The latent curing agent particles can be added to the adhesive as they are, but the non-polar solvent capable of dissolving the main curing agent and the auxiliary curing agent is used as a cleaning liquid, and the latent curing agent particles are immersed in the cleaning liquid for cleaning. Then, the main curing agent and auxiliary curing agent adhering to the surface of the resin particles are removed, so that the storage stability of the adhesive is improved. As described above, since the nonpolar solvent does not enter the resin particles, the main curing agent and the auxiliary curing agent inside the resin particles remain without being removed.
In addition, when it is desired to contain the auxiliary curing agent in the latent curing agent particles at a high concentration, the impregnation liquid may be composed of only the main curing agent and the auxiliary curing agent without adding an organic solvent to the impregnation liquid. .

  The latent curing agent particles containing both the main curing agent and the auxiliary curing agent can cure the adhesive even when no auxiliary curing agent is added to the adhesive. For example, when the main curing agent is a metal chelate or metal alcoholate and the auxiliary curing agent is a silane compound such as a silane coupling agent, if a silane compound is contained in a large amount in a binder, the tackiness of the adhesive decreases and handling becomes difficult. However, if a silane compound is added to the latent curing agent particles, there is no need to add a silane compound to the binder. Can be controlled.

  Silane compounds not only react with metal chelates and metal alcoholates to polymerize resins such as epoxy resins, but also have a high affinity for inorganic substances (eg glass substrates), so silane compounds can be used as latent curing agent particles. By containing, the adhesiveness of the adhesive is also improved.

  Even if the auxiliary curing agent is preliminarily contained in the oil phase liquid, the suspension containing the auxiliary curing agent and the main curing agent is contained inside the resin particles even if the suspension is prepared by the above-described method and the droplets are cured. Hardener particles are obtained.

However, if the auxiliary curing agent is hydrolyzable and the hydrolysis product inhibits the polymerization of the water-reactive monomer or lipophilic monomer, the mechanical strength of the resin particles can be increased by adding the auxiliary curing agent to the oil phase liquid. become weak. Specifically, when the auxiliary curing agent is a silane compound and the water-reactive monomer is an isocyanate, a hydroxyl group is released as a hydrolysis product, and the polymerization of the isocyanate is inhibited by the hydroxyl group.
In the present invention, since the auxiliary curing agent is impregnated after the resin particles are manufactured, the mechanical strength of the resin particles is not weakened, and the auxiliary curing agent is not deteriorated.

The case where the resin particles containing the main curing agent are impregnated with the impregnating liquid has been described above, but the present invention is not limited to this.
For example, it contains no main curing agent, water-reactive monomer polymer, or resin particles composed of water-reactive monomer polymer and lipophilic monomer polymer, and contains main curing agent and auxiliary curing agent. It is also possible to produce latent curing agent particles in which both the main curing agent and the auxiliary curing agent are held on the resin particles by dipping in the impregnation liquid.

The method of impregnating the resin particles with the impregnating liquid is not limited to the method of immersing the resin particles in the impregnating liquid, and the impregnating liquid may be sprayed onto the resin particles.
In this case as well, the latent curing agent particles separated from the impregnating liquid have the main curing agent and the auxiliary curing agent attached to the surface of the resin particles. For example, since the main curing agent and the auxiliary curing agent are removed from the surface of the resin particles, the storage stability of the adhesive is improved when added to the adhesive.
Although the polar solvent used for a washing | cleaning liquid is not specifically limited, For example, cyclohexane, hexane, and toluene can be used individually or in mixture of 2 or more types.

In the impregnating solution, if the solvent that does not decompose the main curing agent is used, or if the main curing agent is liquid, the impregnating solution is prepared without containing any solvent, the impregnating solution is impregnated with resin particles. Neither the main curing agent nor the main curing agent in the resin particles is decomposed.
The polar solvent used for the impregnation liquid is not particularly limited, and for example, ethanol, isopropyl alcohol, ethyl acetate, and methyl ethyl ketone can be used alone or in combination of two or more.

  The lipophilic monomer used in the present invention is not particularly limited as long as it is not reactive with a water-reactive monomer and polymerizes by heating alone or in the presence of a polymerization initiator. Specifically, when the water-reactive monomer is an isocyanate, a bifunctional or more lipophilic monomer having no reactivity with the isocyanate (for example, having a hydroxyl group or the like in the chemical structure) can be widely used.

  Examples of such lipophilic monomers include vinyl monomers such as divinylbenzene, divinyl adipate, vinyl esters and vinyl acetate, and acrylic monomers such as epoxy acrylate, melamine acrylate, urethane acrylate and ester acrylate. When a vinyl monomer or an acrylic monomer is used as the lipophilic monomer, it is desirable to add to the oil phase liquid a radical polymerization initiator that radically polymerizes the monomer by heating.

If resin particles of latent curing agent particles are produced by an interfacial polymerization method, the shape becomes spherical. The particle diameter of the resin particles is preferably 0.5 μm or more and 100 μm or less from the viewpoint of curability and dispersibility.
In terms of curing stability, the latent curing agent particles are substantially free of the organic solvent used during the interfacial polymerization, and specifically, the residual amount of the organic solvent is 1 ppm or less. preferable.

The main curing agent used in the present invention is not particularly limited. For example, when a silane compound is used as the auxiliary curing agent, a metal chelate or a metal alcoholate is used as the main curing agent.
The central metal of the metal chelate and the metal alcoholate is not particularly limited, and various metals such as aluminum, zirconium, and titanium can be used as the central metal, and among these, it is preferable to use an aluminum chelate with particularly high reactivity.
Examples of the aluminum chelating agent used for the main curing agent include complex compounds in which three β-keto enolate anions are represented by the following general formula (1) and coordinated to aluminum.

Here, R ¹ , R ² and R ³ are each independently an alkyl group or an alkoxyl group. Examples of the alkyl group include a methyl group and an ethyl group. Examples of the alkoxyl group include a methoxy group, an ethoxy group, and an oleyloxy group.

  Specific examples of the aluminum chelating agent represented by the chemical formula (1) include aluminum tris (acetylacetonate), aluminum tris (ethylacetoacetate), aluminum monoacetylacetonate bis (ethylacetoacetate), and aluminum monoacetylacetonate. Examples thereof include bisoleyl acetoacetate, ethyl acetoacetate aluminum diisopropylate, and alkyl acetoacetate aluminum diisopropylate.

  The main curing agent contained in the resin particles in advance and the main curing agent contained in the impregnation liquid may be the same type or different types. The resin particles and the impregnation liquid may contain one type of main curing agent, or two or more types of main curing agents.

The water-reactive monomer is not particularly limited as long as it reacts with water and undergoes interfacial polymerization on the surface of the droplet, but specifically, an isocyanate compound is used. The isocyanate compound reacts with water on the droplet surface to produce an intermediate amine, and the amine reacts with the isocyanate to polymerize to produce polyurea. Therefore, when an isocyanate is used for the oil phase liquid, polyurea is generated on the surface of the resin particles.
Among the isocyanate compounds, a polyfunctional isocyanate compound having 2 or more isocyanate groups, preferably 3 isocyanate groups in one molecule is particularly preferable.

  More preferable examples of the trifunctional isocyanate compound include a TMP adduct of the following chemical formula (1) obtained by reacting 3 mol of a diisocyanate compound with 1 mol of trimethylolpropane (TMP), and a chemical formula (2 ) And an isocyanurate body of 3), and a biuret body of the chemical formula (3) obtained by condensing the remaining 1 mole of diisocyanate with diisocyanate urea obtained from 2 moles of 3 moles of the diisocyanate compound.

  In the chemical formulas (1) to (3), the substituent R is a portion excluding the isocyanate group of the diisocyanate compound. Specific examples of such diisocyanate compounds include toluene 2,4-diisocyanate, toluene 2,6-diisocyanate, m-xylylene diisocyanate, hexamethylene diisocyanate, hexahydro-m-xylylene diisocyanate, isophorone diisocyanate, methylene diphenyl-4. , 4'-diisocyanate.

  A resin obtained by interfacial polymerization of such a polyfunctional isocyanate compound is a part of the isocyanate group that undergoes hydrolysis during the interfacial polymerization to become an amino group, which reacts with the amino group to react with the urea bond. It is a polyurea resin that forms a polymer by forming.

  The resin particles composed of a polymer of a water-reactive monomer and a polymer of a lipophilic monomer form a uniform phase inside, and a latent phase composed of such resin particles and a main curing agent held in the phase. When the hardener particles are heated for curing, the clear reason is unknown, but the potential of the retained main curing agent decreases and reacts with the auxiliary curing agent to cause the polymerization reaction of the resin. Can be advanced.

  The latent curing agent particles produced according to the present invention are considered to have a main curing agent also on the outermost surface due to the structure thereof, but the main curing agent present on the outermost surface is a system during interfacial polymerization. It is thought that the activity is weakened by the water present inside. Therefore, the latent hardener particles before washing are considered to have some potential, but in order to further improve the storage stability of the adhesive, before adding the latent hardener particles to the adhesive as described above. It is preferable to wash with a washing solution.

  An organic solvent can be added to the oil phase liquid as necessary. The organic solvent is preferably a volatile organic solvent having a low boiling point. Here, the reason for using the volatile organic solvent is as follows. That is, when a high boiling point solvent having a boiling point exceeding 300 ° C. as used in a normal interfacial polymerization method is used, the organic solvent does not volatilize during the interfacial polymerization, so the contact probability with isocyanate-water does not increase. This is because the degree of progress of interfacial polymerization between them becomes insufficient.

  Therefore, it is difficult to obtain a polymer having good shape retention even when interfacial polymerization is performed, and even when it is obtained, a high boiling point solvent is still taken into the polymer, and when blended in an adhesive, it has a high boiling point. This is because the solvent adversely affects the physical properties of the cured product of the adhesive. For this reason, in this manufacturing method, a volatile thing is used as an organic solvent used when preparing an oil phase.

  Such a volatile organic solvent is a good solvent for each of the main curing agent, the water-reactive monomer, and the lipophilic monomer (the solubility of each is preferably 0.1 g / ml (organic solvent) or more), In particular, it is preferable that it does not substantially dissolve (the solubility of water is 0.5 g / ml (organic solvent) or less) and has a boiling point of 100 ° C. or less under atmospheric pressure. Specific examples of such volatile organic solvents include alcohols, acetate esters, ketones and the like. Among these, ethyl acetate is preferable in terms of high polarity, low boiling point, and poor water solubility.

The amount of the volatile organic solvent used is not particularly limited, but if it is too much, not only will the work environment be adversely affected, but the amount of the main curing agent in the particle will eventually become smaller. It is desirable that the amount be less than the double amount (part by weight) of the functional monomer.
In addition to such a volatile organic solvent, additives such as a surfactant and an antioxidant can be added to the oil phase liquid.

  As the dispersant used in the aqueous phase liquid, in addition to polyvinyl alcohol, those used in usual interfacial polymerization methods such as carboxymethyl cellulose and gelatin can be used. The amount of the dispersant used is usually 0.1% by mass or more and 10.0% by mass or less of the aqueous phase.

  The emulsification conditions for preparing the suspension are, for example, stirring conditions (stirring device homogenizer; stirring speed of 8000 rpm or more) such that the size of the oil phase is preferably 0.5 μm or more and 100 μm or less. Below, the temperature is 30 ° C. or more and 80 ° C. or less, and the stirring time is 2 hours or more and 12 hours or less.

  The latent curing agent particles produced according to the present invention can be used in the same applications as conventional imidazole-based latent curing agent particles. As described above, the auxiliary curing agent, the silane compound, and the main curing agent When used in combination with a resin that is polymerized by the reaction product of the auxiliary curing agent, a low-temperature fast-curing adhesive can be provided.

  As described in paragraphs 0007 to 0010 of JP-A No. 2002-212537, a silane compound that is an auxiliary curing agent is a resin (for example, a thermosetting resin such as an epoxy resin) in cooperation with an aluminum chelating agent. ) To initiate cationic polymerization.

  Such a silane compound has one or more and three or less lower alkoxy groups in the molecule, and a group having reactivity in the molecule with respect to the functional group of the resin in the binder, for example, a vinyl group , Styryl group, acryloyloxy group, methacryloyloxy group, epoxy group, amino group, mercapto group and the like.

  A coupling agent having an amino group or a mercapto group is used when the latent curing agent particle is a cationic main curing agent, so that the amino group or mercapto group does not substantially trap the generated cationic species. be able to.

  Specific examples of such silane compounds include vinyltris (β-methoxyethoxy) silane, vinyltriethoxysilane, vinyltrimethoxysilane, γ-styryltrimethoxysilane, γ-methacryloxypropyltrimethoxysilane, and γ-acryloxy. Propyltrimethoxysilane, β- (3,4-epoxycyclohexyl) ethyltrimethoxysilane, γ-glycidoxypropyltrimethoxysilane, γ-glycidoxypropylmethyldiethoxysilane, N-β- (aminoethyl)- γ-aminopropyltrimethoxysilane, N-β- (aminoethyl) -γ-aminopropylmethyldimethoxysilane, γ-aminopropyltriethoxysilane, N-phenyl-γ-aminopropyltrimethoxysilane, γ-mercaptopropyltri Methoxysilane , Γ-chloropropyltrimethoxysilane and the like.

  As the resin used for the binder of the adhesive, a thermosetting resin, particularly a thermosetting epoxy resin, a thermosetting urea resin, a thermosetting melamine resin, a thermosetting phenol resin, or the like can be used. All of these resins are cationically polymerized by cations that are reaction products. Among these, a thermosetting epoxy resin can be preferably used in consideration of a good adhesive strength after curing.

  Such a thermosetting epoxy resin may be liquid or solid, and preferably has an epoxy equivalent of usually 100 or more and 4000 or less and having two or more epoxy groups in the molecule. For example, a bisphenol A type epoxy compound, a phenol novolac type epoxy compound, a cresol novolac type epoxy compound, an ester type epoxy compound, an alicyclic epoxy compound, or the like can be preferably used. These compounds include monomers and oligomers.

The adhesive can contain a filler such as silica and mica, a pigment, an antistatic agent, and the like as necessary. In addition, the adhesive includes conductive particles having a particle size on the order of several μm, such as metal particles, a resin core surface coated with a metal plating layer, a surface further coated with an insulating thin film, etc. It is preferable to mix | blend with the compounding quantity of 1 mass% or more and 10 mass% or less. Thereby, it becomes possible to use the adhesive manufactured by the manufacturing method of the present invention as an anisotropic conductive adhesive paste and an anisotropic conductive film.
Moreover, the latent hardener particle | grains manufactured by this invention can also be added to the adhesive agent and adhesive film which do not contain electroconductive particle.

<Amount of lipophilic monomer>
As shown in Table 5 to be described later, three types of oil phase liquids were prepared by changing the blending amount of the lipophilic monomer, and three types of suspensions in which the respective oil phase liquids were dispersed in the aqueous phase liquids were 80 ° C. The mixture was stirred while heating to obtain three types of resin particles. The resin particles had a particle size of 5 μm or less (mode diameter of about 2.3 μm). The compositions of the oil phase liquid and the aqueous phase liquid are shown in Tables 1 and 2 below.

  After separating the resin particles from the aqueous phase liquid, each of the three types of resin particles was immersed in an impregnating liquid having the composition shown in Table 3 below, and heated and stirred at 30 ° C. for 6 hours to impregnate the resin particles with the impregnating liquid. The latent curing agent particles of Examples 1 to 3 were obtained.

  The latent curing agent particles were separated from the impregnating solution, immersed in cyclohexane, which is a nonpolar solvent, and washed, and then the latent curing agent particles were separated from the nonpolar solvent and dried to remove the organic solvent. Using the latent curing agent particles of Examples 1 to 3 after drying, three types of adhesives were prepared at the blending ratios shown in Table 4 below.

Next, the three types of resin particles before impregnating the latent curing agent particles of Examples 1 to 3 with the impregnating liquid were used as latent curing agent particles of Comparative Examples 1 to 3, respectively. Using the curing agent particles, among the compositions in Table 4 above, only 3 parts by weight of the auxiliary curing agent was used to prepare three types of adhesives.
About these 6 types of adhesive agents, DSC analysis (Differential scanning calorimetry, differential scanning calorimetry) was performed on the conditions of the temperature increase rate of 5 degree-C / min.

The DSC chart of the adhesive using the latent curing agent particles of Comparative Examples 1 to 3 is not shown in FIG. 1, and the DSC chart of the adhesive using the latent curing agent particles of Examples 1 to 3 is not occupied in FIG. . Incidentally, reference numerals C _1, C _2, C ₃ in Figure 1 is a DSC chart of the case of using a latent curing agent particles of Comparative Examples 1 to 3 respectively, the sign of FIG. 2 E _1, E _2, E ₃ is a DSC chart when the latent curing agent particles of Examples 1 to ₃ are used, respectively.

The rise of the DSC chart indicates that the polymerization reaction of the resin has started, and the peak of the DSC chart indicates that the polymerization reaction has reached the peak.
Table 5 below shows the temperature at which the DSC chart rises (curing start temperature), the temperature at which the chart reaches a peak (exothermic peak temperature), and the maximum intensity (exothermic peak intensity) of the DSC chart together with the DVB substitution rate.

  The DVB substitution rate is a value obtained by dividing the blending amount (weight) of DVB (divinylbenzene) by the sum of the blending amount of DVB and the blending amount of isocyanate by 100, and the DVB substitution rate is that of Example 1. Comparative Example 1 is 0%, Example 2 and Comparative Example 2 are 30%, Example 3 and Comparative Example 3 are 40%.

  As is clear from FIGS. 1 and 2 above, when the latent curing agent particles of Examples 1 to 3 are used, the DSC chart is sharp and the exothermic peak intensity is high compared to Comparative Examples 1 to 3. . The higher the exothermic peak intensity of the DSC chart, the faster the curing rate of the adhesive. It can be seen that the curing rate of the adhesive is increased by impregnating the resin particles with the main curing agent.

  The resin particles before impregnating the impregnating liquid had a tendency to increase the curing start temperature and the exothermic peak temperature as the divinylbenzene content increased. The variation is gone. This is probably because the resin particles containing the main curing agent are impregnated with the main curing agent in advance, so that a uniform distribution of the main curing agent is formed at the center portion and the surface portion of the resin particles. .

  Moreover, when the curing start temperature of Examples 1 to 3 is seen, the curing start temperature is higher than room temperature, but is in a relatively low temperature region, and has storage stability at room temperature, but is cured at a relatively low temperature when heated. I understand.

Since the latent curing agent particles produced according to the present invention contain a main curing agent that is not hydrolyzed inside the resin particles, the resin can be polymerized even if the amount of the auxiliary curing agent added to the adhesive is small. .
For example, as described above, the adhesive was cured at a low temperature with 1 part by weight of the auxiliary curing agent with respect to 2 parts by weight of the latent curing agent particles in Examples 1 to 3, but the resin particles not impregnated were cured at a low temperature. Required 12 parts by weight of auxiliary curing agent for 2 parts by weight of the resin particles.

<Main curing agent concentration>
The latent curing agent of Examples 4 and 5 under the same conditions as in Example 2 (DVB substitution rate 30%) except that the aluminum chelate concentration in the impregnation liquid was changed from 30% by weight to 20% by weight and 40% by weight. Particles were created.

  Using the latent curing agent particles of Examples 4 and 5, two types of adhesives were prepared with the composition shown in Table 4 above, and the latent curing agent particles of Examples 1 to 3 were used for these adhesives. DSC analysis was performed under the same conditions. The DSC chart is shown in FIG. 3, and “curing start temperature”, “exothermic peak temperature”, and “exothermic peak intensity” are shown in Table 6 below together with the measurement results of Example 2.

  As is clear from FIG. 3 and Table 6 above, increasing the concentration of the main curing agent decreases the curing start temperature and the exothermic peak temperature, and the low temperature curability of the adhesive is advanced. From these facts, it is understood that the curing temperature of the adhesive can be controlled by changing the main curing agent concentration in the impregnating liquid.

<Auxiliary curing agent-containing latent curing agent particles>
The same as in Example 2 except that four types of impregnating liquids were prepared by changing the content of the auxiliary curing agent in the impregnating liquid having the composition described in Table 7 below, and the impregnating liquids were respectively changed to these four types of impregnating liquids. Under the conditions, the latent curing agent particles of Examples 6 to 9 were prepared.

  Using the latent curing agent particles of Examples 6 to 9 and Example 2 above, a total of 10 types of adhesives were prepared with the compositions described in Table 4 and the compositions described in Table 8 below.

  DSC analysis was performed using these 10 types of adhesives. FIG. 4 shows a DSC chart of an adhesive (composition of Table 4) in which an auxiliary curing agent is added to the binder, and FIG. 5 shows a DSC chart of an adhesive (composition of Table 8) in which no auxiliary curing agent is added to the binder. The “curing start temperature”, “exothermic peak temperature”, and “exothermic peak intensity” of each adhesive are shown in Table 9 below together with the content of the auxiliary curing agent in the impregnating liquid.

  In Table 9, the “curing start temperature”, “exothermic peak temperature”, and “exothermic peak intensity” columns are the values outside the parentheses, which are values of the adhesive in which an auxiliary curing agent is added to the binder. The numerical value of is the value of the adhesive in which no auxiliary curing agent was added to the binder.

  As can be seen from Table 9 and FIGS. 4 and 5, as the content of the auxiliary curing agent in the impregnating solution increases, both the curing start temperature and the exothermic peak temperature are lowered, and the effect of the lowering is shown in FIG. 5. As shown, it was remarkable when an auxiliary curing agent was not contained in the binder.

  The potential of Example 9 using the impregnating liquid consisting of the main curing agent, the diluting solvent originally added to the main curing agent product, and the auxiliary curing agent without adding the diluting solvent shown in Table 7 to the impregnating liquid. The functional hardener particles were able to achieve a low temperature of 61 ° C. as a curing start temperature even in a binder containing no auxiliary hardener.

On the contrary, in Example 2 in which the auxiliary curing agent was not added to the impregnation liquid, the adhesive was not cured when the auxiliary curing agent was not added to the binder. From this result, it was confirmed that by adding an auxiliary curing agent to the impregnating solution, a curing reaction of the adhesive occurs without adding an auxiliary curing agent to the binder.
Further, in the electron micrograph of the latent curing agent particles of Example 9 above, the resin particles were not deformed or aggregated, and it was confirmed that the particle state after the impregnation liquid immersion treatment was good.

<Type of auxiliary curing agent>
Four types of impregnating solutions were prepared by changing the type of the auxiliary curing agent of the impregnating solution described in Table 7 above, and Examples 10 to 13 were performed under the same conditions as in Example 9 except that these four types of impregnating solutions were used. Latent curing agent particles were made. The product name of the auxiliary curing agent (silane compound) and the type of functional group are shown in Table 10 below.

  Each silane compound described in Table 10 is a product of Shin-Etsu Chemical Co., Ltd.

Using Examples 10 to 13 and the latent curing agent particles of Example 9, a total of 10 types of adhesives having the compositions shown in Tables 4 and 8 were prepared, and DSC analysis was performed on each adhesive.
DSC analysis was performed using these 10 types of adhesives. FIG. 6 shows a DSC chart of an adhesive (composition of Table 4) in which an auxiliary curing agent is added to the binder, and FIG. 7 shows a DSC chart of an adhesive (composition of Table 8) in which no auxiliary curing agent is added to the binder. The “curing start temperature”, “exothermic peak temperature”, and “exothermic peak intensity” of each adhesive are shown in Table 10 above together with the type of auxiliary curing agent in the impregnating liquid.

  In Table 10, the “curing start temperature”, “exothermic peak temperature”, and “exothermic peak intensity” columns are the values outside the parentheses, which are values of the adhesive obtained by adding an auxiliary curing agent to the binder. The numerical value of is the value of the adhesive in which no auxiliary curing agent was added to the binder.

  As shown in FIG. 7, in the case of Example 11 using a silane compound having a glycidyl group, low temperature curability having a curing start temperature of 53 ° C. and an exothermic peak temperature of 86 ° C. could be achieved. This is thought to be due to the fact that the epoxy polymerization efficiency was increased by making the silane compound having a reactive epoxy group latent with the aluminum chelate as the main curing agent.

  Similarly, Example 13 using a silane compound having a cyclohexene oxide group which is an alicyclic epoxy group also had a tendency to cure at low temperature. Since both the cyclohexene oxide group and the glycidyl group are epoxy groups, and the latent curing agent particles impregnated with the silane compound having these epoxy groups are very active, an adhesive containing a small amount of the silane compound in the binder, As shown in FIG. 6, the curing start temperature decreased to the 40 ° C. range.

  In addition, when a vinyl type silane compound is used, the exothermic peak becomes a double peak because the difference in the ligand substitution amount of the aluminum chelating agent by the silane compound may have an effect. . That is, in a vinyl-type silane compound with small steric hindrance, ligand substitution is likely to occur, and two types of cationic species with different reactivity may be generated by reaction with an aluminum chelate.

<Reference test 1>
11 parts by weight of a 24% isopropanol solution of aluminum monoacetylacetonate bis (ethyl acetoacetate) (trade name “aluminum chelate D” manufactured by Kawaken Fine Chemical Co., Ltd.) and methylenediphenyl-4,4′-diisocyanate (3 Mole) of trimethylolpropane (1 mol) adduct (trade name “D-109” manufactured by Mitsui Takeda Chemical Co., Ltd.) was dissolved in 11 parts by weight of 30 parts by weight of ethyl acetate as an organic solvent. An oil phase solution was obtained.

  This oil phase liquid was mixed with the aqueous phase liquid described in Table 1 above, emulsified and mixed with a homogenizer (11000 rpm / 10 minutes), and then subjected to interfacial polymerization at 60 ° C. overnight. After the completion of the reaction, the polymerization reaction solution was allowed to cool to room temperature, and the interfacially polymerized particles were separated by filtration and naturally dried to obtain spherical resin particles having a particle size of about 10 μm.

The resin particles were impregnated in the impregnation liquid described in Table 3 above to prepare the latent curing agent particles of Example 14.
As a comparative control, the latent curing agent particles of Comparative Example 4 were prepared under the same conditions as in Example 14 except that the oil phase liquid did not contain aluminum chelate.

  Using the latent curing agent particles of Example 14 and Comparative Example 4, an adhesive was prepared with the composition of Table 4, and the DSC analysis was performed on the adhesive under the conditions of a heating rate of 5 ° C./min and a measurement amount of 10 mg. It was. As a result of DSC analysis, the obtained DSC chart is shown in FIG. 8, and the values of the curing start temperature, exothermic peak temperature and exothermic peak intensity read from the DSC chart are shown in Table 11 below.

  8 indicates a DSC chart when the latent hardener particles of Example 14 are used, and C4 in FIG. 8 indicates a DSC chart when the latent hardener particles of Comparative Example 4 are used. Yes.

  As is clear from Table 11 and the chart of FIG. 8, Comparative Example 4 has a higher heat generation start temperature and a higher thermosetting temperature than Example 14, and is inferior in the low-temperature curability of the adhesive. This is because there is a limit to the amount of the aluminum chelate impregnated even if the resin chelate containing no aluminum chelate is impregnated later, and compared with Example 14, the latent curing agent particles of Comparative Example 4 It is presumed that the aluminum chelate content was reduced.

<Reference test 2>
Five types of impregnating liquids having the compositions shown in Table 7 were prepared by changing the amount of the silane coupling agent. The blending amount of the silane coupling agent is shown in Table 12 below.

The latent curing agent particles of Examples 15 to 19 were produced by immersing the resin particles produced under the same conditions as in Example 14 in the five types of impregnation liquids.
In addition, since the lipophilic monomer is not added to the oil phase liquid used in Example 14, and the latent curing agent particles of Example 14 have a DVB substitution rate of zero, the potentials of Examples 15 to 19 are eliminated. The DVB substitution rate of the curing agent particles is also zero.

  Using the latent curing agent particles of Examples 15 to 19, an adhesive was produced with the composition shown in Table 4 above, and DSC analysis of the adhesive was performed. As a result of the DSC analysis, the obtained DSC chart is shown in FIG. 9, and the curing start temperature, exothermic peak temperature, and exothermic peak intensity values read from the DSC chart are shown in Table 12 above.

Symbols E _{15 to} E _{19 in} FIG. 9 show DSC charts when the latent curing agent particles of Examples 15 to ₁₉ are used, respectively.
As can be seen from FIG. 9 and Table 12, when the amount of the silane coupling agent is up to 20 parts by weight, the curing start temperature and the exothermic peak temperature are lowered as the amount of the silane coupling agent is increased. When the amount exceeds 20 parts by weight, the curing start temperature and the exothermic peak temperature shifted to the high temperature side.

  On the other hand, when the lipophilic monomer is contained in the oil phase liquid (Examples 2 to 6, Table 9, and FIG. 4), the curing start temperature is set even when the amount of the silane coupling agent exceeds 20 parts by weight. The exothermic peak temperature is decreasing.

  This is because when the resin particles are produced without containing the lipophilic monomer in the oil phase liquid, the crosslink density of the polyurea-urethane bond is too high compared to the case where the lipophilic monomer is contained, and the silane coupling agent is This is presumably because the amount of resin particles that can be impregnated becomes small.

<Reference test 3>
The latent curing agent particles of Examples 15 to 19 and a binder not containing a silane coupling agent were blended with the composition shown in Table 8 to prepare five types of adhesives.
DSC analysis was performed using these adhesives. As a result of DSC analysis, the obtained DSC chart is shown in FIG. 10, and the curing start temperature, exothermic peak temperature, and exothermic peak intensity read from the DSC chart of FIG. 10 are shown together with the amount of the silane coupling agent in the impregnating liquid. Are listed in Table 13 below.

Incidentally, it shows a DSC chart of the adhesive using the latent curing agent particles of the code E ₁₅ to E ₁₉ are examples 15 to 19 in FIG. 10.

  As can be seen from Table 13 and FIG. 10, the curing start temperature and the exothermic peak temperature are lower as the amount of the silane coupling agent in the impregnating solution is increased. In addition, since the latent curing agent particles of Example 15 did not contain a silane coupling agent, the curing reaction did not occur with an adhesive to which no silane coupling agent was added even in the binder.

  In addition, the measurement results (Tables 12 and 13) when the lipophilic monomer was not added to the oil phase liquid in the process of producing the resin particles, and the lipophilic monomer were added to the oil phase liquid in the process of producing the resin particles. In comparison with the case results (Table 9), even when the compounding amount of the silane coupling agent in the impregnating liquid is the same, the case where the lipophilic monomer is added to the oil phase liquid is compared with the case where it is not added. The exothermic peak intensity tended to be high.

  The higher the exothermic peak strength is, the faster the curing rate of the adhesive is. Therefore, it can be seen that the curing rate of the adhesive is faster when the lipophilic monomer is added to the oil phase liquid in the process of producing the resin particles. .

  The higher the content of the silane coupling agent, the faster the curing speed. Therefore, in the process of producing resin particles, adding lipophilic monomer to the oil phase liquid has the ability to penetrate and retain the silane coupling agent. It can be seen that high resin particles can be obtained.

  From the above, it can be seen that it is preferable to add a lipophilic monomer to the oil phase liquid in order to produce an adhesive that can be cured at a low temperature for a short time.

DSC chart when the latent curing agent particles of Comparative Examples 1 to 3 are added to the adhesive DSC chart when latent curing agent particles of Examples 1 to 3 are added to the adhesive DSC chart when latent curing agent particles of Examples 2, 4, and 5 are added to adhesive DSC chart when the latent curing agent particles of Examples 2 and 6 to 9 are added to an adhesive containing an auxiliary curing agent DSC chart when latent curing agent particles of Examples 2 and 6 to 9 are added to an adhesive containing no auxiliary curing agent DSC chart when latent curing agent particles of Examples 9 to 13 are added to an adhesive containing an auxiliary curing agent DSC chart when latent curing agent particles of Examples 9 to 13 are added to an adhesive containing no auxiliary curing agent DSC chart when the latent curing agent of Example 14 and Comparative Example 4 was added to the adhesive DSC chart when latent curing agent particles of Examples 15 to 19 are added to an adhesive containing an auxiliary curing agent DSC chart when latent curing agent particles of Examples 15 to 19 are added to an adhesive containing no auxiliary curing agent

Claims (15)

Latent curing agent particles for producing latent curing agent particles to be dispersed in an adhesive, wherein the reaction product with an auxiliary curing agent contains a main curing agent that cures the adhesive A manufacturing method of
A raw material liquid production process for producing a raw material liquid having a reactive resin capable of polymerization reaction and the main curing agent;
Resin particle production step of producing the resin particles containing the main curing agent by heating the raw material liquid to polymerize the reactive resin;
An impregnation step of bringing the resin particles into contact with an impregnation liquid to which the main curing agent is added, impregnating the resin particles with the main curing agent, and increasing the content of the main curing agent in the resin particles; A process for producing latent curing agent particles having The auxiliary curing agent is a substance that inhibits polymerization of the reactive resin,
The method for producing latent curing agent particles according to claim 1, wherein the impregnation liquid contains the auxiliary curing agent.   The latent material according to claim 1, wherein the raw material liquid production step includes a dispersion step of dispersing the reactive resin and the main curing agent in a main solvent that decomposes the main curing agent. A method for producing curing agent particles.   A reactive monomer that can be polymerized by reacting with the main solvent and a thermally polymerizable monomer that forms droplets in the main solvent are used as the reactive resin and dispersed in the main solvent together with the main curing agent. Item 4. A process for producing latent curing agent particles according to Item 3.   The method for producing latent curing agent particles according to claim 4, wherein the auxiliary curing agent inhibits a polymerization reaction of the reactive monomer.   The method for producing latent curing agent particles according to any one of claims 3 to 5, wherein a main component of water is used as the main solvent.   The method for producing latent curing agent particles according to claim 6, wherein the reactive monomer is an isocyanate.   The method for producing latent curing agent particles according to claim 4, wherein the thermally polymerizable monomer is one or both of a vinyl monomer and an acrylic monomer. The main curing agent is a metal chelate;
The method for producing latent curing agent particles according to any one of claims 1 to 8, wherein the auxiliary curing agent is a silane compound.   9. The cleaning step of immersing the latent curing agent particles in a cleaning solution that dissolves the main curing agent and does not penetrate into the resin particles is provided after the impregnation step. A process for producing latent curing agent particles according to claim 1.   The method for producing latent curing agent particles according to claim 10, wherein the polymer of the reactive monomer is a polar resin, and the cleaning liquid is a nonpolar solvent. The polymer of the reactive monomer is a polyurea resin,
The method for producing latent curing agent particles according to claim 11, wherein the cleaning liquid contains one or more polar solvents selected from the group consisting of cyclohexane, hexane, and toluene.   The manufacturing method of the adhesive agent which disperse | distributes the said latent hardener particle | grains manufactured with the manufacturing method of any one of Claim 1 thru | or 12 to the binder containing resin and the organic solvent.   The method for producing an adhesive according to claim 13, wherein the auxiliary curing agent is contained in the binder.   The adhesion | attachment which removes the said organic solvent from the said application layer, and forms the said application layer after forming the application layer of the said adhesive agent manufactured with the manufacturing method of any one of Claim 13 or Claim 14 A method for producing a film.

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