JP2835401B2 - Two-component adhesive - Google Patents

Description

Description: TECHNICAL FIELD The present invention relates to a two-part adhesive.

Conventional technology and its problems having a hydroxyl group or a hydrolyzable group bonded to a silicon atom,
A cured positive resin composition mainly composed of a rubber organic polymer having at least one silicon atom-containing group capable of crosslinking by forming a siloxane bond (hereinafter referred to as “reactive silicon group”) and an epoxy resin, It is known before the filing of the present application (JP-A-61-268720).

However, according to the study of the present inventor, when the resin composition is used as a two-part adhesive, that is, the rubber organic polymer is used as one component, and a curing catalyst for an epoxy resin and a rubber organic polymer is used. When used as a two-component adhesive as the other component, the following disadvantages have been found to occur. That is, the latter component has poor storage stability, and therefore, when the composition is used as one component of a two-part adhesive after being left for a long period of time, the curing speed of the adhesive becomes slow, and the curing reaction is rapid. It was found that it was impossible to proceed. This tendency is remarkable when a filler, particularly an inorganic filler, is contained in the component containing the epoxy resin.

Means for Solving the Problems In view of this situation, the present inventors have intensively studied to develop a two-part adhesive having excellent storage stability. As a result, it has been found that the intended object of the present invention can be achieved when an acidic filler is blended with the epoxy resin-containing component. The present invention has been completed based on such findings.

That is, the present invention provides (A) a composition containing (1) a rubber-based organic polymer having at least one reactive silicon group and (2) an epoxy resin curing agent (hereinafter, referred to as “composition A”); (B) A two-component adhesive comprising a composition containing (1) an epoxy resin, (2) a curing catalyst for the rubber-based organic polymer, and (3) an acidic filler (hereinafter referred to as “composition B”). According to.

In the present invention, the composition A contains a rubber organic polymer having at least one reactive silicon group and an epoxy resin curing agent.

Examples of the polymer constituting the skeleton of the rubber-based organic polymer having at least one reactive silicon group include polyethers obtained by polymerization of cyclic ethers such as propylene oxide, ethylene oxide and tetrahydrofuran; dibasic acids such as adipic acid Polyesters obtained by condensation of ethylene with glycol or ring-opening polymerization of lactones; ethylene-propylene copolymers; polyisobutylene or copolymers of isobutylene and isoprene; polychloroprene; polyisoprene or isoprentobutadiene, styrene, Copolymers with acronitrile and the like; polybutadienes or copolymers with butadiene and styrene, acrylonitrile and the like; polyisoprenes, polybutadienes or polyolefins obtained by hydrogenating copolymers of isoprene and butadiene; Relate, polyacrylic acid ester or the acrylic ester and vinyl acetate monomer such as butyl acrylate obtained by radical polymerization,
Copolymers such as acrylonitrile, styrene, ethylene, etc .; graft polymers obtained by polymerizing vinyl monomers in the rubber organic polymer used in the present invention; polymers such as polysulfides; Among them, a general formula such as a polypropylene oxide-based polyether or the like: -RO- wherein R represents a divalent alkylene group having 2 to 4 carbon atoms. A copolymer such as a graft polymer obtained by polymerizing a vinyl monomer such as an acrylate, styrene, acrylonitrile, or vinyl acetate in the presence of a polyether having a repeating unit represented by A polymer, a copolymer of alkyl polyacrylate or alkyl acrylate containing 50% by weight or more of alkyl acrylate and vinyl acetate, acrylonitrile, styrene, ethylene, etc., introduces a reactive silicon group into a molecular terminal. It is preferable from the viewpoints of easy production and easy production of a liquid polymer without solvent.

In the present invention, the reactive silicon group is not particularly limited, but typical examples thereof include those represented by the general formula (1) Wherein R ¹ and R ² are each a hydrocarbon group having 1 to 20 carbon atoms or (R ′) ₃ SiO— (R ′ is a monovalent hydrocarbon group having 1 to 20 carbon atoms; R ′ may be the same or different), and when two or more R ¹ or R ² are present, they may be the same; It may be different. X represents a hydroxyl group or a hydrolyzable group, and when two or more Xs are present,
They may be the same or different. a
Represents 0, 1, 2 or 3, and b represents 0, 1 or 2. Also m B need not be the same. m is 0 or 1 to 19
Indicates an integer. However, it is assumed that a + (sum of b) ≧ 1 is satisfied. ] The group represented by these is mentioned.

When X is a hydroxyl group, the reactive silicon group undergoes a silanol condensation reaction in the presence or absence of a silanol condensation catalyst to form a crosslink. When X is a hydrolyzable group, the reactive silicon group undergoes a hydrolysis reaction and a quilanol condensation reaction with moisture in the presence or absence of a silanol condensation catalyst to form a crosslink.

The hydrolyzable group represented by X is not particularly limited, and includes a conventionally known hydrolyzable group, and specifically includes, for example, a hydrogen atom, a halogen atom, an alkoxy group, an acyloxy group, a ketoximate group, an amino group Groups, amide groups, acid amide groups, aminooxy groups, mercapto groups, alkenyloxy groups and the like. Of these, a hydrogen atom, an alkoxy group, an acyloxy group, a ketoximate group, an amino group, an amide group, an aminooxy group, a mercapto group and an alkenyloxy group are preferred. Is particularly preferred.

The hydrolyzable group or hydroxyl group can be bonded to one silicon atom in the range of 1 to 3 and the sum of (a + b) is 1 to 5
Is preferable. When two or more hydrolyzable groups or hydroxyl groups are bonded to the reactive silicon group, they may be the same or different.

The number of silicon atoms forming the reactive silicon group may be one or two or more. In the case of silicon atoms connected by a siloxane bond or the like, the number may be up to about 20. In particular, general formula (2) Wherein R ² , X and a are the same as above. ] Is preferable from the viewpoint of availability.

In addition, the carbon number of R ¹ and R ² in the above general formula (1) is 1
Examples of the monovalent hydrocarbon group having from 20 to 20 include an alkyl group having 1 to 20 carbon atoms, an aryl group having 6 to 20 carbon atoms, an aralkyl group having 7 to 20 carbon atoms, and more specifically, a methyl group. And an alkyl group such as ethyl group, a silcoalkyl group such as cyclohexyl group, an aryl group such as phenyl group, and an aralkyl group such as benzyl group. Specific examples of the triorganosiloxy group include a triorganosiloxy group represented by (R ') ₃ SiO- wherein R' is a methyl group, a phenyl group, or the like. Of these, a methyl group is particularly preferred.

The reactive silicon group is chemically bonded to the rubber-based organic polymer main chain. In the bond between the reactive silicon group and the main chain of the rubber-based polymer, the presence of a bond such as a Si—O—C bond is not desirable because the bond may be broken by moisture. Among the reactive silicon groups, the silicon atom closest to the rubber-based organic polymer main chain is preferably bonded by a Si—O—C bond.

It is preferable that at least one, preferably 1.2 to 6 reactive silicon groups be present in one molecule of the rubber-based organic polymer. When the number of the opposite silicon groups contained in the molecule is less than one, the curability becomes insufficient, and it becomes difficult to exhibit good rubber elasticity behavior.

The reactive silicon group may be present at the terminal of the molecular chain of the rubber-based organic polymer, may be present internally, or may be present at both. In particular, when the reactive silicon group is present at the molecular chain end, the molecular chain length between the cross-linking points in the formed cured product becomes longer, so that the rubber elasticity characteristics are likely to appear effectively,
Therefore, the epoxy resin blended in the direct agent of the present invention is preferred in that the brittleness is easily improved, while a rubber cured product mainly composed of a rubber-based organic polymer is easily obtained in high strength.

The introduction of the reactive silicon group into the rubber-based organic polymer may be performed by a known method, for example, the following methods (1) to (4).

(1) Monomers having a copolymerizable unsaturated group and a reactive silicon group such as vinyl trialkoxysilane, methacryloyloxypropylmethyl dialkoxysilane, methacryloyloxypropyl trialkoxysilane and the like in the molecule are ethylene, propylene, Epoxy groups that can be copolymerized with polymerizable monomers such as isobutylene, chloroprene, isoprene, butadiene, and acrylic acid esters, and copolymerizable epoxy groups such as γ-glycidoxypropyltrimethoxysilane and γ-glycoxypropylmethyldimethoxysilane And a method of copolymerizing a monomer containing a reactive silicon group in a molecule with propylene oxide or ethylene oxide.

By this method, a reactive silicon group can be introduced into a molecular side chain.

(2) Chain transfer of a compound having a reactive silicon group and a mercapto group or a disulfide group such as mercaptopropyl trialkoxysilane or mercaptopropylmethyldialkoxysilane which can cause a chain transfer reaction in radical polymerization. A method of polymerizing a radically polymerizable monomer by using it as an agent.

(3) Azobis-2- (8-methyldiethoxysilyl-
A method of polymerizing a radically polymerizable monomer using an azo or peroxide polymerization initiator containing a reactive silicon group such as 2-cyanohexane).

In the methods (2) and (3), a reactive silicon group is introduced into a polymer molecule terminal.

(4) A polymer having a functional group such as a hydroxyl group, a carboxyl group, a mercapto group, an epoxy group, or an isocyanate group (hereinafter, referred to as “Y functional group”) on a side chain and / or a terminal of the polymer is used. A method in which a compound containing a functional group capable of reacting with a group in a molecule and having a reactive silicon group is reacted with a Y functional group.

Specific examples of the rubber-based organic polymer used in the present invention include, for example, JP-B Nos. 45-36319 and 12154, and
No. 32673, gazette, the same 46-JP-A-50-156599,
JP-A-51-73561, JP-A-54-6098, JP-A-55-13767, JP-A-54-13768, JP-A-55-82123, and JP-A-55-82123
No. 123820, No. 55-125121, No. 55-131021, No. 55-131022, No. 55-135135, No. 55-131
No. 137129, No. 57-179210, No. 58-191703, No. 59-78220, No. 59-78221, No. 59-78
Nos. 222, 59-78223, 59-168014, and the like.

The number average molecular weight of the rubber organic polymer having a reactive silicon group is preferably about 500 to 50,000, and 1,000 to
About 20000 is particularly preferred. In the present invention, such a rubber-based organic polymer may be used alone or in combination of two or more.

In the present invention, as the epoxy resin curing agent blended in the composition A, a commonly used curing agent for epoxy resin can be widely used. Specifically, triethylenetetramine, tetraethylenepentamine, diethylaminopropylamine, N-aminoethylpiperazine, m-xylylenediamine, m-phenylenediamine, diaminodiphenylmethane, diaminodiphenylsulfone, isophoronediamine, 2,4,6 Amines such as tris (dimethylaminomethyl) phenol; tertiary amine salts; polyamide resins; imidazoles; dicyandiamides;
Boron trifluoride complex compounds; phthalic anhydride such as phthalic anhydride, hexahydrophthalic anhydride, tetrahydrophthalic anhydride, endomethylenetetrahydrophthalic anhydride, dodecinyl succinic anhydride, pyromellitic anhydride, chlorenoic anhydride; alcohols Phenols; carboxylic acids and the like. In the present invention, such a curing agent is
One type is used alone, or two or more types are used in combination.

In the present invention, the mixing ratio of the rubber organic polymer and the epoxy resin curing agent blended in the composition A is not particularly limited, but the epoxy resin curing agent is mixed from the composition B. 100 parts by weight of epoxy resin
Usually, it is good to be blended so as to be about 0.1 to 300 parts by weight, preferably about 0.5 to 100 parts by weight.

In the present invention, the composition B contains an epoxy resin, a curing catalyst for the rubber-based organic polymer, and an acidic filler.

As the epoxy resin blended in the composition B, conventionally known epoxy resins can be widely used, for example, flame retardants such as epichlorohydrin-bisphenol A epoxy resin, epichlorohydrin-bisphenol F epoxy resin, and glycidyl ether of tetrabromobisphenol A. Epoxy resin, novolak epoxy resin, hydrogenated bisphenol A epoxy resin, glycidyl ether epoxy resin of bisphenol A propylene oxide adduct, p-
Glycidyl oxybenzoate ether type epoxy resin, m-aminophenol epoxy resin, diaminodiphenylmethane epoxy resin, urethane-modified epoxy resin, various alicyclic epoxy resins, N, N-diglycidylaniline, N, N-diglycidyl- Examples include glycidyl ethers of polyhydric alcohols such as o-toluidine, triglycidyl isocyanurate, polyalkylene glycol diglycidyl ether, and glycerin, and epoxy compounds of unsaturated polymers such as hydantoin type epoxy resins and petroleum resins. Among these, especially the formula Those containing at least two epoxy groups in the molecule represented by are preferred from the viewpoints of high reactivity during curing and easy formation of a three-dimensional network in the cured product. In the present invention, bisphenol A type epoxy resins and novolak type epoxy resins are most preferred. In the present invention, such epoxy resins are used singly or as a mixture of two or more.

As the curing catalyst blended in the composition B, those conventionally known as silanol condensation catalysts can be widely used. Specific examples thereof include titanates such as tetrabutyl titanate and tetrapropyl titanate; tin carboxylates such as dibutyltin dilaurate, dibutyltin maleate, dibutyltin diacetate, tin octylate, tin naphthenate; dibutyltin oxide and phthalic acid Reactant with ester; dibutyltin diacetylacetonate; organic aluminum compounds such as aluminum trisacetylacetonate, aluminum trisethylacetoacetate, diisopropoxyaluminum ethylacetoacetate; zirconium tetraacetylacetonate, titanium tetraacetylacetonate, etc. Chelating compounds; lead octylate; butylamine,
Octylamine, dibutylamine, monoethanolamine, diethanolamine, triethanolamine, diethylenetriamine, triethylenetetramine, oleylamine, cyclohexylamine, benzylamine, diethylaminopropylamine, xylylenediamine, triethylenediamine, guanidine, diphenylguanidine, 2,4, 6-tris (dimethylaminomethyl) phenol, morpholine, N-methylmorpholine, 2-ethyl-
4-methylimidazole, 1,8-diazabicyclo (5,4,
0) amine compounds such as undecene-7 (DBU) or salts thereof with carboxylic acids and the like; low molecular weight polyamide resins obtained from excess polyamine and polybasic acid; reaction formation between excess polyamine and epoxy compound A silane coupling agent having an amino group, for example, a silanol condensation catalyst such as γ-aminopropyltrimethoxysilane and N- (β-aminoethyl) aminopropylmethyldimethoxysilane, as well as many acidic catalysts and basic catalysts Known silanol condensation catalysts. These catalysts may be used alone or in combination of two or more.

As the acidic filler to be blended in the composition B, those that when dispersed in water, the pH of the water becomes in an acidic region (for example, 100 c
As long as the pH of the water is in the acidic range by dispersing 10 g of the filler in water of c), conventionally known ones can be widely used, for example, titanium dioxide, silica, clay and the like. These are used alone or in combination of two or more. In the present invention, it is essential to mix an acidic filler in the composition HB. Even if an alkaline filler such as calcium carbonate or magnesium carbonate is blended in place of the acidic filler, the intended object of the present invention cannot be achieved. However, as long as the acidic filler is blended in the composition B, it is possible to blend a filler other than the acidic filler such as the alkaline filler in the composition A or the composition B. Yes, even in this case, the intended purpose of the present invention can be sufficiently achieved. As fillers that can be blended, for example, wood flour,
Examples include pulp, cotton chips, asbestos, glass fiber, carbon fiber, mica, walnut shell powder, graphite, carbon black, calcium carbonate, talc, magnesium carbonate, quartz, aluminum fine powder, flint powder, zinc powder and the like.

In the present invention, the mixing ratio of the curing catalyst and the acidic filler to the epoxy resin mixed in the composition B is not particularly limited. However, with respect to the epoxy resin, the weight ratio of the rubber-based organic polymer / epoxy resin used in the composition A is about 1/100 to 100/1, particularly 10/10 to 100/10.
It is good to mix so that it becomes the degree. If the amount of the epoxy resin is too small, the mechanical strength such as the elastic modulus of the obtained cured product tends to be insufficient, and if the amount of the epoxy resin is too large, the obtained cured product is brittle. Tend to be unfavorable. Further, the curing catalyst is used for the rubber organic polymer mixed from the composition A.
Usually, it is good to mix so as to be about 0.1 to 20 parts by weight, preferably about 0.5 to 10 parts by weight. Further, the amount of the acidic filler is usually about 1 to 500 parts by weight, preferably about 10 to 300 parts by weight, based on 100 parts by weight of the total amount of the rubber organic polymer and the epoxy resin. The amount of the acidic filler contained in the composition B is preferably about 1 to 90% by weight, more preferably about 5 to 70% by weight in the composition B. If the amount of the acidic filler is too small, the effect of improving the storage stability is reduced, and if the amount of the acidic filler is too large, the composition is not liquid and the workability is poor. Tend to occur, both of which are undesirable. When fillers other than acidic fillers are used, the total amount of the filler is 1 to 100 parts by weight of the total amount of the rubber organic polymer and the epoxy resin.
It is preferable that the composition B contains a large amount of the acidic filler, for example, 30% by weight or more, particularly 50% by weight or more of the total amount of the filler in the composition B. .

The composition A or the composition B of the present invention further contains various plasticizers, an antioxidant, an ultraviolet absorber, a lubricant, a content, if necessary.
A foaming agent and the like can be blended.

There is no particular limitation on the use of the two-part adhesive of the present invention, and it can be made in the same manner as the conventional two-part adhesive.

Effects of the Invention According to the present invention, even when a filler is blended in a composition containing an epoxy resin and a curing catalyst, a two-part adhesive excellent in storage stability can be obtained.

Examples Examples will be given below to further clarify the present invention. In the following, simply “parts” means “parts by weight”,
“%” Means “% by weight”.

Production Example 1 90 parts of polypropylene glycol (number average molecular weight 2500) and 10 parts of polypropylene triol (number average molecular weight 3000)
Part as a starting material, and after performing a molecular weight jump reaction using methylene chloride, the allyl ether group obtained by capping the molecular chain terminal with acryl chloride is introduced into 99% of all terminals. 800 g of polypropylene oxide was placed in a pressure-resistant reaction vessel equipped with a stirrer, and 20 g of methyldimethoxysilane was added. Then chloroplatinic acid catalyst solution _{(H 2 PtCl 6 · 6H 2} O Isopropyl alcohol 8.9g of 1
Solution dissolved in 8 ml and 160 ml of tetrahydrofuran).
After adding 40 ml, the mixture was reacted at 80 ° C. for 6 hours.

When the amount of the remaining silicon hydride groups in the reaction solution was quantified by an IR spectrum analysis method, almost no silicon hydride groups remained. When the silicon group was quantified by the NMR method, Was obtained in about 1.57 per molecule.

Production Example 2 Starting from polypropylene glycol (number-average molecular weight 2000), methylene chloride was used to perform a molecular weight jump reaction, and then allyl ether groups obtained by capping the molecular chain terminals with allyl chloride were converted to all terminals. 95
% Of polypropylene oxide having a number average molecular weight of 5000 introduced into a pressure-resistant reaction vessel equipped with a stirrer, and 32 g of triethoxysilane was added. Next, 0.40 ml of a chloroplatinic acid catalyst solution (same composition as in Production Example 1) was added, and the mixture was reacted at 90 ° C. for 3 hours. After removing excess silane under reduced pressure, the amount of silicon was quantified by NMR, and (CH ₃ CH ₂ O) ₃
A polypropylene oxide having about 1.8 SiCH ₂ CH ₂ CH ₂ O-molecules per molecule was obtained.

Production Example 3 300 g of polypropylene glycol having a number average molecular weight of 3000 was charged into a plastic stirrer, and 26 g of tolylene diisocyanate and 0.2 g of dibutyltin dilaurate were added.
The reaction was carried out at 00 ° C. for 5 hours while stirring under a nitrogen gas stream. Then γ-aminopropyltriethoxysilane 22.1
g was added thereto and reacted while stirring at 100 ° C. for 3 hours to obtain a polyether having an average molecular weight of about 6,600, a triethoxysilyl machine at a terminal, and having about two reactive silicon groups in the molecule.

Production Example 4 80 g of butyl acrylate, stearyl methacrylate 2
0 g, γ-methacryloyloxypropylmethyldimethoxysilane 2.2 g, γ-mercaptopropylmethyldimethoxysilane 1.8 g and 2,2′-azobisisobutyronitrile
0.5 g was mixed and stirred to dissolve uniformly. 25 g of the mixture
Was placed in a 200 ml four-necked flask equipped with a stirrer and a condenser, and heated to 80 ° C. in an oil bath while passing nitrogen gas. After a few minutes, polymerization started and heat was generated. After the heat generation became mild, the remaining mixed solution was gradually dropped over 3 hours using a dropping funnel to carry out polymerization. After the dropping, 15 minutes and 30 minutes later, 0.15 g of AIBN was added. After the addition, stirring was continued for 30 minutes to terminate the polymerization reaction.

When the obtained liquid polymer was analyzed by gel permeation chromatography (GPC), the number average molecular weight was about 1
It was 0000.

Example 1 and Comparative Example 1 Preparation of Liquid A 100 parts of the polymer obtained in Production Example 1, 2,2'-methylene-bis- (4-methyl-6-t-butylphenol) 1
Part, N-β- (aminoethyl) -γ-aminopropyltrimethoxysilane 1 part, vinyltrimethoxysilane 3
Parts, 46 parts of heavy calcium carbonate and 5 parts of 2,4,6-tris- (dimethylaminomethyl) phenol are mixed well using a three paint roll to obtain a mixture.

Preparation of Liquid B Epicoat 828 (bisphenol A type epoxy resin manufactured by Yuka Shell Epoxy Co., Ltd.) 50 parts, heavy calcium carbonate 25 parts, # 918 (organotin compound, Sankyokisei Co., Ltd.)
1 part and Aerosil R-202 (Nippon Aerosil Co., Ltd.)
Two parts are mixed well with a three paint roll to obtain a formulation.

Solution A and Solution B are each placed in a sealed glass container,
After storing at 50 ° C. for one month, 20 g of solution A and 10 g of solution B were mixed and cured at 23 ° C. and 50% RH, and the surface curing time (tack free time in contact) was measured.

Table 1 shows the results of measuring the tack-free time in the same manner as in Comparative Example 1, except that Aerosil R-202 was not used in Solution B. Table 1 shows that the storage stability is significantly improved by adding Aerosil R-202.

In Example 1, a mixture of 40 g of the liquid A and 20 g of the liquid B was evaluated as an adhesive according to JIS K 6850 and JIS K 6854. JIS H 4000 for tensile shear strength measurement
Using an aluminum plate A-1050P (100 × 25 × 2 mm test piece), the above mixture was applied with a spatula, stuck together, and pressed by hand to produce a test sample. T-peel strength is JIS
Using a H4000 aluminum plate A1050P (200 × 25 × 0.1 mm test piece), apply the above mixture with a spatula to a thickness of about 0.5 mm and stick it together. Do not reciprocate in the length direction using a 5 kg hand roller. Was pressed five times to produce a test sample. These adhesion test samples were cured and cured at 23 ° C. for 2 days and further at 50 ° C. for 3 days and subjected to a tensile test. The tensile speed was 50 mm / min for tensile shear, and 200 mm / min for T-shaped peeling. The adhesion strength of the adhesion test sample prepared using the solution A and the solution B after storage at 50 ° C. for one month is shown in Table 1. In Comparative Example 1, the strength was reduced. Example 1 has the same strength as before storage.

Examples 2 to 7 The results obtained in the same manner as in Example 1 except that various acidic fillers were used in place of 2 parts of Aerosil R-202 in the solution B of Example 1 are referred to as Examples 2 to 7. The results are shown in Table 2.

Examples 8 to 10 In the solution A of Example 1, except that the polymer of Production Examples 2 to 4 was used instead of the polymer obtained in Production Example 1,
In the same manner as in Example 1, the results of tack-free measurement are shown in Table 3 as Examples 8 to 10.

 ────────────────────────────────────────────────── ─── Continuation of the front page (72) Katsuhiko Isayama, Inventor 4-8-7 Chikushigaoka, Kita-ku, Kobe-shi, Hyogo (56) References JP-A-63-97675 (JP, A) JP-A-58-47054 (JP) , A) JP-A-61-83220 (JP, A)

Claims (1)

(57) [Claims] (A) (1) A rubber-based organic polymer having a hydroxyl group or a hydrolyzable group bonded to a silicon atom and having at least one silicon atom-containing group which can be crosslinked by forming a siloxane bond. And (2) a composition containing an epoxy resin curing agent, and (B) a composition containing (1) an epoxy resin, (2) a curing catalyst for the rubber-based organic polymer, and (3) an acidic filler. Two-part adhesive.