JP2012211299A - Curable composition - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a curable composition which exhibits excellent curability, adhesiveness, and storage stability and which does not require an organotin-type catalyst and is therefore highly safe.SOLUTION: The curable composition includes (A) an organic polymer which contains on average 0.8 or more crosslinking silicon group in one molecule and in which the main chain is not a polysiloxane, (B) a silane compound obtained by reacting a specific epoxysilane compound with a specific aminosilane compound at a ratio such that the amount of the epoxysilane compound is in the range of 1.5-10 mol relative to one mol of the aminosilane compound, and (C) a specific titanium catalyst, with the amounts of the silane compound (B) and the titanium catalyst (C) being 0.1-40 pts.mass and 0.1-40 pts.mass respectively relative to 100 pts.mass of the organic polymer (A).

Description

  The present invention relates to an organic polymer having a silicon-containing group (hereinafter also referred to as “crosslinkable silicon group”) having a hydroxyl group or a hydrolyzable group bonded to a silicon atom and capable of crosslinking by forming a siloxane bond. It relates to the curable composition containing this.

  An organic polymer containing at least one crosslinkable silicon group in the molecule is crosslinked at room temperature by the formation of a siloxane bond accompanied by a hydrolysis reaction of a reactive silicon group due to moisture or the like. It is known to have the property of being obtained. Among these polymers having a crosslinkable silicon group, organic polymers whose main chain skeleton is a polyoxyalkylene polymer or a (meth) acrylate polymer are used for sealing materials, adhesives, paints, etc. Widely used.

  The curable composition used for sealing materials, adhesives, paints, etc. and the rubber-like cured product obtained by curing have various properties such as curability, adhesiveness, storage stability, mechanical properties such as modulus, strength, and elongation. Properties are required, and many studies have been made on organic polymers containing crosslinkable silicon groups.

  These curable compositions containing an organic polymer having a crosslinkable silicon group are cured using a silanol condensation catalyst. Usually, organic tin-based catalysts such as dibutyltin bis (acetylacetonate) are widely used. in use. However, in recent years, toxicity of organotin compounds has been pointed out, and development of non-organotin catalysts has been demanded.

As this non-organotin-based catalyst, a dealcohol-free silicone composition using a titanium catalyst is already commercially available and widely used for many applications (for example, Patent Documents 1 to 3).
However, there are relatively few examples of adding a titanium catalyst to an organic polymer containing a crosslinkable silicon group, which are disclosed in Patent Documents 4 to 21 and the like. The curable compositions using these titanium catalysts have a problem that the curing rate is slow, and the curing rate is lowered and the viscosity is increased after storage.

  Moreover, the curable composition containing the organic polymer containing a crosslinkable silicon group is often used as an adhesive or a sealing material, and in that case, adhesion to various types of substrates is required. In order to ensure this adhesion, so-called aminosilane having a primary amino group and an alkoxy group in the molecule is usually used. However, when an organic polymer containing a crosslinkable silicon group and a titanium catalyst are used to prepare a one-component curable composition by adding aminosilane, the composition is good after storage for a certain period, although the adhesiveness is good. If the viscosity of the product is improved and it is severe, it may harden in the container and cannot be used. Sealing materials and adhesives are not always used immediately after production, but are often stored for several months in warehouses or stores, and it is desired that their curability and viscosity be constant before and after storage. Yes.

Japanese Examined Patent Publication No. 39-27643 US Pat. No. 3,175,993 US Pat. No. 3,334,067 JP 58-17154 A JP-A-11-209538 JP-A-5-311063 JP 2001-302929 A JP 2001-302930 A JP 2001-302931 A JP 2001-302934 A JP 2001-348528 A Japanese Patent Laid-Open No. 2002-249672 JP 2003-165916 A JP 2003-147220 A JP 2005-325314 A WO2005 / 108492 WO2005 / 108498 WO2005 / 108494 WO2005 / 108499 WO2007 / 037368 JP 2008-280434 A

  An object of this invention is to provide the curable composition excellent in sclerosis | hardenability, adhesiveness, and storage stability, and excellent in safety | security without requiring an organic tin-type catalyst.

  In order to solve the above-mentioned problems, the present inventors have conducted intensive research and have identified, as a curing catalyst, an organic polymer containing 0.8 or more crosslinkable silicon groups on average in one molecule. By using a silane compound obtained by reacting an epoxy silane compound and a specific aminosilane compound in combination with a titanium chelate coordinated with a β-ketoester, it has excellent curability, adhesiveness and storage stability, and It has been found that a room temperature moisture-curable curable composition that does not require an organotin catalyst and is excellent in safety can be obtained.

That is, the curable composition of the present invention is (A) an organic polymer containing 0.8 or more crosslinkable silicon groups on average in one molecule and the main chain is not polysiloxane, (B) An epoxysilane compound represented by (1) and an aminosilane compound represented by the following formula (2) are reacted with 1 mol of the aminosilane compound within a range of 1.5 to 10 mol of the epoxysilane compound. A silane compound, and (C) one or more titanium catalysts selected from the group consisting of a titanium chelate represented by the following formula (3) and a titanium chelate represented by the following formula (4):
The curable composition containing 0.1 to 40 parts by mass of the (B) silane compound and 0.1 to (C) the titanium catalyst with respect to 100 parts by mass of the (A) organic polymer. It is characterized by blending 40 parts by mass.

(In the formula (1), R ^{1 to} R ³ are each a hydrogen atom or an alkyl group, R ⁴ is an alkylene group or an alkyleneoxyalkylene group, R ⁵ is a monovalent hydrocarbon group, and R ⁶ is An alkyl group, and a is 0, 1 or 2.)

(In the formula (2), R ^{7 to} R ¹² are each a hydrogen atom or an alkyl group, R ¹³ is a monovalent hydrocarbon group, R ¹⁴ is an alkyl group, and b is 0 or 1. )

(In the formula (3), n R ^{21 s} are independently substituted or unsubstituted hydrocarbon groups having 1 to 20 carbon atoms, and 4-n R ^{22 s} are independently hydrogen atoms. Or a substituted or unsubstituted hydrocarbon group having 1 to 20 carbon atoms, wherein 4-n R ²³ and 4-n R ²⁴ are independently substituted or unsubstituted carbon atoms having 1 to 20 carbon atoms. And n is 0, 1, 2 or 3.)

(In the formula (4), R ²⁵ is a substituted or unsubstituted divalent hydrocarbon group having 1 to 20 carbon atoms, and the two R ²⁶ are independently hydrogen atoms or substituted or unsubstituted. And 2 R ²⁷ and 2 R ²⁸ are each independently a substituted or unsubstituted hydrocarbon group having 1 to 20 carbon atoms.)

  The (B) silane compound is preferably a silane compound obtained by reacting the epoxysilane compound and the aminosilane compound at a reaction temperature of 40 to 100 ° C.

  The (A) organic polymer is a polyoxyalkylene polymer containing 0.8 or more crosslinkable silicon groups on average per molecule, and 0.8 or more crosslinks on average per molecule. Selected from the group consisting of a saturated hydrocarbon polymer containing a functional silicon group and a (meth) acrylic acid ester polymer containing an average of 0.8 or more crosslinkable silicon groups in one molecule. One or more are preferable.

  It is preferable that the crosslinkable silicon group includes a trimethoxysilyl group.

  The curable composition of the present invention preferably further contains (D) a silane compound having one hydrolyzable silicon group and one primary amino group in one molecule. The (D) silane compound is preferably a compound represented by the following formula (12).

In the formula (12), R ⁴¹ is a methyl group or an ethyl group, and when a plurality of R ⁴¹ are present, they may be the same or different, and R ⁴² is a methyl group or An ethyl group, and when there are a plurality of R ^{42 s} , they may be the same or different, R ⁴³ is a hydrocarbon group having 1 to 10 carbon atoms, and m is 2 or 3 and n is 0 or 1.

  The curable composition of the present invention preferably further contains (E) a filler. The filler (E) is at least one selected from the group consisting of surface-treated calcium carbonate, amorphous silica having a particle size of 0.01 to 300 μm, and polymer powder having a particle size of 0.01 to 300 μm. It is preferable.

  A curable composition excellent in transparency by matching the difference in refractive index so that the difference between the refractive index of the organic polymer (A) and the refractive index of the amorphous silica is 0.1 or less. You can get things.

Further, the difference in refractive index between the liquid phase component (A) containing the organic polymer as a main component and the refractive index of the polymer powder is made to be equal to or less than 0.1. Thus, a curable composition having excellent transparency can be obtained.
By adding a refractive index adjusting agent to the (A) organic polymer, the difference between the refractive index of the liquid phase component mainly composed of the (A) organic polymer and the refractive index of the polymer powder is 0.1. The following is preferable.

  The polymer powder polymerizes a monomer selected from the group consisting of (meth) acrylic acid ester, vinyl acetate, ethylene and vinyl chloride alone, or the monomer and one or more vinyl monomers The polymer powder is preferably a polymer powder obtained from a polymer obtained by copolymerization, and is at least one selected from the group consisting of an acrylic polymer powder and a vinyl polymer powder. More preferred.

  The curable composition of the present invention preferably further contains (F) a diluent.

  The curable composition of the present invention preferably further contains a metal hydroxide. It is preferable that the metal hydroxide is aluminum hydroxide.

  ADVANTAGE OF THE INVENTION According to this invention, the curable composition excellent in sclerosis | hardenability, adhesiveness, and storage stability and excellent in safety | security without requiring an organic tin-type catalyst can be provided. Moreover, according to this invention, the curable composition excellent in transparency can also be obtained.

  Embodiments of the present invention will be described below, but these are exemplarily shown, and it goes without saying that various modifications are possible without departing from the technical idea of the present invention.

  The curable composition of the present invention comprises (A) an organic polymer containing 0.8 or more crosslinkable silicon groups on average in one molecule and whose main chain is not polysiloxane, (B) the above formula (1) ) And an aminosilane compound represented by the above formula (2) are reacted in a range of 1.5 to 10 mol with respect to 1 mol of the aminosilane compound. And (C) a curable composition comprising at least one titanium catalyst selected from the group consisting of a titanium chelate represented by the formula (3) and a titanium chelate represented by the formula (4). The (B) silane compound is 0.1 to 40 parts by mass and the (C) titanium catalyst is 0.1 to 40 parts by mass with respect to 100 parts by mass of the (A) organic polymer. To do.

  The (A) organic polymer is an organic polymer containing 0.8 or more crosslinkable silicon groups on average in one molecule and the main chain is not polysiloxane, and various main chain bones excluding polysiloxane. You can use one with a rating.

  Specifically, polyoxyalkylene heavy polymers such as polyoxyethylene, polyoxypropylene, polyoxybutylene, polyoxytetramethylene, polyoxyethylene-polyoxypropylene copolymer, polyoxypropylene-polyoxybutylene copolymer, etc. Copolymer; ethylene-propylene copolymer, polyisobutylene, copolymer of isobutylene and isoprene, polychloroprene, polyisoprene, isoprene or copolymer of butadiene and acrylonitrile and / or styrene, polybutadiene, isoprene or butadiene A copolymer of acrylonitrile and styrene, etc., a hydrocarbon polymer such as a hydrogenated polyolefin polymer obtained by hydrogenating these polyolefin polymers; a dibasic acid such as adipic acid and a glycol; Polyester polymers obtained by condensation or ring-opening polymerization of lactones; (meth) acrylic acid ester polymers obtained by radical polymerization of monomers such as ethyl (meth) acrylate and butyl (meth) acrylate; (Meth) acrylic acid ester monomers, vinyl polymers obtained by radical polymerization of monomers such as vinyl acetate, acrylonitrile, styrene, etc .; graft polymers obtained by polymerizing vinyl monomers in the organic polymers; polysulfides Polymer: Nylon 6 by ring-opening polymerization of ε-caprolactam, nylon 6.6 by condensation polymerization of hexamethylenediamine and adipic acid, nylon 6.10 by condensation polymerization of hexamethylenediamine and sebacic acid, ε-aminoundecanoic acid Nylon 11, ε-aminolaurolacta by condensation polymerization A polyamide polymer such as nylon 12 by ring-opening polymerization of the above, a copolymer nylon having two or more components among the above-mentioned nylons; for example, a polycarbonate polymer produced by condensation polymerization of bisphenol A and carbonyl chloride, diallyl Examples thereof include phthalate polymers.

  Furthermore, saturated hydrocarbon polymers such as polyisobutylene, hydrogenated polyisoprene, and hydrogenated polybutadiene, polyoxyalkylene polymers, and (meth) acrylic acid ester polymers can be obtained with a relatively low glass transition temperature. A cured product is preferred because of its excellent cold resistance. Polyoxyalkylene polymers and (meth) acrylic acid ester polymers are particularly preferred because of their high moisture permeability and excellent deep-part curability when made into one-component compositions.

  The crosslinkable silicon group of the (A) organic polymer used in the present invention is a group having a hydroxyl group or a hydrolyzable group bonded to a silicon atom and capable of crosslinking by forming a siloxane bond. As the crosslinkable silicon group, for example, a group represented by the following general formula (5) is preferable.

In the formula (5), R ³¹ is an alkyl group having 1 to 20 carbon atoms, a cycloalkyl group having 3 to 20 carbon atoms, an aryl group having 6 to 20 carbon atoms, an aralkyl group having 7 to 20 carbon atoms, or R ^31. ₃ represents a triorganosiloxy group represented by SiO— (R ³¹ is the same as above), and when two or more R ³¹ are present, they may be the same or different. X represents a hydroxyl group or a hydrolyzable group, and when two or more X exist, they may be the same or different. d represents 0, 1, 2, or 3, and e represents 0, 1, or 2, respectively. Further, p in the following general formula (6) need not be the same. p shows the integer of 0-19. However, d + (sum of e) ≧ 1 is satisfied.

The hydrolyzable group or hydroxyl group can be bonded to one silicon atom in the range of 1 to 3, and d + (sum of e) is preferably in the range of 1 to 5. When two or more hydrolyzable groups or hydroxyl groups are bonded to the crosslinkable silicon group, they may be the same or different.
The number of silicon atoms forming the crosslinkable silicon group may be one or two or more, but in the case of silicon atoms linked by a siloxane bond or the like, there may be about 20 silicon atoms.

  As the crosslinkable silicon group, a crosslinkable silicon group represented by the following general formula (7) is preferable because it is easily available.

In the formula (7), R ³¹ and X are the same as those described above, and d is an integer of 1, 2 or 3. In view of curability, in order to obtain a curable composition having a sufficient curing rate, a in the formula (7) is preferably 2 or more, and more preferably 3.

Specific examples of R ³¹ include alkyl groups such as methyl and ethyl groups, cycloalkyl groups such as cyclohexyl groups, aryl groups such as phenyl groups, aralkyl groups such as benzyl groups, and R ³¹ ₃ SiO—. And triorganosiloxy group. Of these, a methyl group is preferred.

  It does not specifically limit as a hydrolysable group shown by said X, What is necessary is just a conventionally well-known hydrolysable group. Specific examples include a hydrogen atom, a halogen atom, an alkoxy group, an acyloxy group, a ketoximate group, an amino group, an amide group, an acid amide group, an aminooxy group, a mercapto group, and an alkenyloxy group. Among 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 preferable, and an alkoxy group, an amide group, and an aminooxy group are more preferable. An alkoxy group is particularly preferred from the viewpoint of mild hydrolysis and easy handling. Among the alkoxy groups, those having a smaller number of carbon atoms have higher reactivity, and the reactivity increases as the number of carbon atoms increases in the order of methoxy group> ethoxy group> propoxy group. Although it can be selected according to the purpose and use, a methoxy group or an ethoxy group is usually used.

Specific examples of the crosslinkable silicon group include trialkoxysilyl groups [—Si (OR) ₃ ] such as trimethoxysilyl group and triethoxysilyl group, dialkoxy such as methyldimethoxysilyl group and methyldiethoxysilyl group. A silyl group [—SiR ¹ (OR) ₂ ], and a trimethoxysilyl group is more preferable. Here, R is an alkyl group such as a methyl group or an ethyl group.

  Further, the crosslinkable silicon group may be used alone or in combination of two or more. The crosslinkable silicon group can be present in the main chain, the side chain, or both.

  The number of silicon atoms forming the crosslinkable silicon group is one or more, but in the case of silicon atoms linked by a siloxane bond or the like, it is preferably 20 or less.

  The organic polymer having a crosslinkable silicon group may be linear or branched, and its number average molecular weight is about 500 to 100,000 in terms of polystyrene in GPC, more preferably 1,000 to 50,000. And particularly preferably 3,000 to 30,000. If the number average molecular weight is less than 500, the cured product tends to be disadvantageous in terms of elongation characteristics, and if it exceeds 100,000, the viscosity tends to be inconvenient because of high viscosity.

  In order to obtain a rubber-like cured product having high strength, high elongation, and low elastic modulus, the average number of crosslinkable silicon groups contained in the organic polymer is 0.8 or more in one molecule of the polymer. 1.1 to 5 may be present. If the number of crosslinkable silicon groups contained in the molecule is less than 0.8 on average, the curability becomes insufficient and it becomes difficult to develop good rubber elastic behavior. The crosslinkable silicon group may be at the end of the main chain or the side chain of the organic polymer molecular chain, or at both ends. In particular, when the crosslinkable silicon group is only at the end of the main chain of the molecular chain, the effective network length of the organic polymer component contained in the finally formed cured product is increased, so that the strength and elongation are high. It becomes easy to obtain a rubber-like cured product exhibiting a low elastic modulus.

The polyoxyalkylene polymer is essentially a polymer having a repeating unit represented by the following general formula (8).
-R ³² -O- (8)
In the general formula (8), R ³² is a linear or branched alkylene group having 1 to 14 carbon atoms, preferably a linear or branched alkylene group having 1 to 14 carbon atoms, and more preferably 2 to 4 carbon atoms. .

Specific examples of the repeating unit represented by the general formula (8) include
_{-CH 2 O -, - CH 2} CH 2 O -, - CH 2 CH (CH 3) O -, - CH 2 CH (C 2 H 5) O -, - CH 2 C (CH 3) 2 O-, _{-CH 2 CH 2 CH 2 CH 2} O-
Etc. The main chain skeleton of the polyoxyalkylene polymer may be composed of only one type of repeating unit, or may be composed of two or more types of repeating units. In particular, when used as a sealant or the like, a polymer comprising a propylene oxide polymer as a main component is preferable because it is amorphous or has a relatively low viscosity.

  As a method for synthesizing a polyoxyalkylene polymer, for example, a polymerization method using an alkali catalyst such as KOH, for example, JP-A Nos. 61-197631, 61-215622, 61-215623, and 61-215623 can be used. Polymerization method using an organoaluminum-porphyrin complex catalyst obtained by reacting an organoaluminum compound and a porphyrin as shown, for example, a double metal cyanide complex shown in JP-B-46-27250 and JP-B-59-15336 Examples of the polymerization method using a catalyst include, but are not limited to, a polymerization method. A polyoxyalkylene system having a narrow molecular weight distribution with a high molecular weight having a number average molecular weight of 6,000 or more and Mw / Mn of 1.6 or less according to a polymerization method using an organic aluminum-porphyrin complex catalyst or a polymerization method using a double metal cyanide complex catalyst A polymer can be obtained.

  The main chain skeleton of the polyoxyalkylene polymer may contain other components such as a urethane bond component. Examples of the urethane bond component include aromatic polyisocyanates such as toluene (tolylene) diisocyanate, diphenylmethane diisocyanate, xylylene diisocyanate; aliphatic polyisocyanates such as isophorone diisocyanate and hexamethylene diisocyanate; The thing obtained from reaction with coalescence can be mention | raise | lifted.

  The introduction of a crosslinkable silicon group into a polyoxyalkylene polymer can be performed on a polyoxyalkylene polymer having a functional group such as an unsaturated group, a hydroxyl group, an epoxy group or an isocyanate group in the molecule. The reaction can be carried out by reacting a compound having a reactive functional group and a crosslinkable silicon group (hereinafter referred to as a polymer reaction method).

  As a specific example of the polymer reaction method, a hydrosilane or mercapto compound is produced by reacting an unsaturated group-containing polyoxyalkylene polymer with a hydrosilane having a crosslinkable silicon group or a mercapto compound having a crosslinkable silicon group. The method of obtaining the polyoxyalkylene type polymer which has this can be mention | raise | lifted. An unsaturated group-containing polyoxyalkylene polymer is obtained by reacting an organic polymer having a functional group such as a hydroxyl group with an organic compound having an active group and an unsaturated group that are reactive with the functional group, A polyoxyalkylene polymer containing can be obtained.

  Other specific examples of the polymer reaction method include a method of reacting a polyoxyalkylene polymer having a hydroxyl group at a terminal with a compound having an isocyanate group and a crosslinkable silicon group, or a polyoxyalkylene system having an isocyanate group at a terminal. Examples thereof include a method of reacting a polymer with a compound having an active hydrogen group such as a hydroxyl group or an amino group and a crosslinkable silicon group. When an isocyanate compound is used, a polyoxyalkylene polymer having a crosslinkable silicon group can be easily obtained.

  Specific examples of the polyoxyalkylene polymer having a crosslinkable silicon group include JP-B Nos. 45-36319, 46-12154, JP-A Nos. 50-156599, 54-6096, and 55-13767. No. 57-164123, JP-B No. 3-2450, JP-A No. 2005-213446, No. 2005-306891, International Publication No. WO2007-040143, US Pat. No. 3,632,557, No. 4,345,053, The ones proposed in the publications such as 4,960,844 can be listed.

  The above polyoxyalkylene polymers having a crosslinkable silicon group may be used alone or in combination of two or more.

  The saturated hydrocarbon polymer is a polymer that does not substantially contain a carbon-carbon unsaturated bond other than an aromatic ring, and the polymer constituting the skeleton thereof is (1) ethylene, propylene, 1-butene, isobutylene, (2) A diene compound such as butadiene or isoprene is homopolymerized, or a copolymer with the olefin compound is copolymerized. After that, it can be obtained by a method such as hydrogenation. However, isobutylene polymers and hydrogenated polybutadiene polymers are easy to introduce functional groups at the terminals, control the molecular weight, and the number of terminal functional groups. Therefore, an isobutylene polymer is particularly preferable.

  Those whose main chain skeleton is a saturated hydrocarbon polymer have characteristics of excellent heat resistance, weather resistance, durability, and moisture barrier properties.

  In the isobutylene-based polymer, all of the monomer units may be formed from isobutylene units, or may be a copolymer with other monomers, but the repeating unit derived from isobutylene is 50 from the viewpoint of rubber properties. Those containing at least mass% are preferred, those containing at least 80 mass% are more preferred, and those containing from 90 to 99 mass% are particularly preferred.

  As a method for synthesizing a saturated hydrocarbon polymer, various polymerization methods have been reported so far, but in particular, many so-called living polymerizations have been developed in recent years. In the case of saturated hydrocarbon polymers, particularly isobutylene polymers, the inifer polymerization found by Kennedy et al. (JP Kennedy et al., J. Polymer Sci., Polymer Chem. Ed. 1997, 15, 2843) It is known that it can be easily produced by using it, it can be polymerized with a molecular weight of about 500 to 100,000 with a molecular weight distribution of 1.5 or less, and various functional groups can be introduced at the molecular ends.

  Examples of the method for producing a saturated hydrocarbon polymer having a crosslinkable silicon group include, for example, Japanese Patent Publication No. 4-69659, Japanese Patent Publication No. 7-108928, Japanese Patent Publication No. 63-254149, Japanese Patent Publication No. 64-22904, Although described in each specification of Kaihei 1-197509, Japanese Patent Publication No. 2539445, Japanese Patent Publication No. 2873395, and Japanese Patent Application Laid-Open No. 7-53882, it is not particularly limited thereto.

  The above saturated hydrocarbon polymer having a crosslinkable silicon group may be used alone or in combination of two or more.

  It does not specifically limit as a (meth) acrylic-ester type monomer which comprises the principal chain of the said (meth) acrylic-ester type polymer, A various thing can be used. Examples include (meth) acrylic acid, methyl (meth) acrylate, ethyl (meth) acrylate, n-propyl (meth) acrylate, isopropyl (meth) acrylate, n-butyl (meth) acrylate, Isobutyl (meth) acrylate, tert-butyl (meth) acrylate, n-pentyl (meth) acrylate, n-hexyl (meth) acrylate, cyclohexyl (meth) acrylate, n-heptyl (meth) acrylate, N-octyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, nonyl (meth) acrylate, decyl (meth) acrylate, dodecyl (meth) acrylate, phenyl (meth) acrylate, (meth) acrylic Acid toluyl, benzyl (meth) acrylate, 2-methoxyethyl (meth) acrylate, (meth) acrylic 3-methoxybutyl, 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, stearyl (meth) acrylate, glycidyl (meth) acrylate, 2-aminoethyl (meth) acrylate, γ -(Methacryloyloxypropyl) trimethoxysilane, γ- (methacryloyloxypropyl) dimethoxymethylsilane, methacryloyloxymethyltrimethoxysilane, methacryloyloxymethyltriethoxysilane, methacryloyloxymethyldimethoxymethylsilane, methacryloyloxymethyldiethoxymethylsilane, (Meth) acrylic acid ethylene oxide adduct, (meth) acrylic acid trifluoromethyl methyl, (meth) acrylic acid 2-trifluoromethyl ethyl, (meth) acrylic acid 2- -Fluoroethylethyl, 2-perfluoroethyl-2-perfluorobutylethyl (meth) acrylate, perfluoroethyl (meth) acrylate, trifluoromethyl (meth) acrylate, bis (trifluoro) (meth) acrylate Methyl) methyl, (meth) acrylic acid 2-trifluoromethyl-2-perfluoroethylethyl, (meth) acrylic acid 2-perfluorohexylethyl, (meth) acrylic acid 2-perfluorodecylethyl, (meth) acrylic Examples include (meth) acrylic acid monomers such as 2-perfluorohexadecylethyl acid.

  In the (meth) acrylic acid ester polymer, the following vinyl monomer can be copolymerized together with the (meth) acrylic acid ester monomer. Examples of the vinyl monomer include styrene monomers such as styrene, vinyl toluene, α-methyl styrene, chlorostyrene, styrene sulfonic acid, and salts thereof; fluorine-containing vinyl monomers such as perfluoroethylene, perfluoropropylene, and vinylidene fluoride. Silicon-containing vinyl monomers such as vinyltrimethoxysilane and vinyltriethoxysilane; maleic anhydride, maleic acid, monoalkyl and dialkyl esters of maleic acid; fumaric acid, monoalkyl and dialkyl esters of fumaric acid; maleimide, Methyl maleimide, ethyl maleimide, propyl maleimide, butyl maleimide, hexyl maleimide, octyl maleimide, dodecyl maleimide, stearyl maleimide, phenyl maleimide, cyclohexyl Maleimide monomers such as maleimide; Nitrile group-containing vinyl monomers such as acrylonitrile and methacrylonitrile; Amide group-containing vinyl monomers such as acrylamide and methacrylamide; Vinyl acetate, vinyl propionate, vinyl pivalate, vinyl benzoate, cinnamon Examples thereof include vinyl esters such as vinyl acid; alkenes such as ethylene and propylene; conjugated dienes such as butadiene and isoprene; vinyl chloride, vinylidene chloride, allyl chloride, and allyl alcohol.

  These may be used alone or a plurality of these may be copolymerized. Especially, the polymer which consists of a styrene-type monomer and a (meth) acrylic-acid type monomer is preferable from the physical property of a product. More preferred is a (meth) acrylic polymer comprising an acrylate monomer and a methacrylic acid ester monomer, and particularly preferred is an acrylic polymer comprising an acrylate monomer. In applications such as general construction, a butyl acrylate monomer is more preferred from the viewpoint that physical properties such as low viscosity of the blend, low modulus of the cured product, high elongation, weather resistance, and heat resistance are required. On the other hand, in applications that require oil resistance, such as automobile applications, copolymers based on ethyl acrylate are more preferred. This polymer mainly composed of ethyl acrylate is excellent in oil resistance but tends to be slightly inferior in low-temperature characteristics (cold resistance). It is also possible to replace it. However, as the ratio of butyl acrylate is increased, its good oil resistance is impaired. Therefore, for applications requiring oil resistance, the ratio is preferably 40% or less, and more preferably 30% or less. More preferably. It is also preferred to use 2-methoxyethyl acrylate or 2-ethoxyethyl acrylate in which oxygen is introduced into the side chain alkyl group in order to improve the low temperature characteristics without impairing oil resistance. However, since heat resistance tends to be inferior due to the introduction of an alkoxy group having an ether bond in the side chain, when heat resistance is required, the ratio is preferably 40% or less. In accordance with various uses and required purposes, it is possible to obtain suitable polymers by changing the ratio in consideration of required physical properties such as oil resistance, heat resistance and low temperature characteristics. For example, although not limited, examples of excellent physical property balance such as oil resistance, heat resistance, and low temperature characteristics include ethyl acrylate / butyl acrylate / -2-methoxyethyl acrylate (40-50 / 20 by mass ratio). To 30/30 to 20). In the present invention, these preferable monomers may be copolymerized with other monomers, and further block copolymerized, and in this case, it is preferable that these preferable monomers are contained in a mass ratio of 40% or more. . In the above expression format, for example, (meth) acrylic acid represents acrylic acid and / or methacrylic acid.

  In the present invention, the method for obtaining the (meth) acrylic acid ester polymer is not particularly limited, and known polymerization methods (for example, JP-A-63-112642, JP-A-2007-230947, JP-A-2001-40037). And a synthesis method described in JP-A-2003-313397), and a radical polymerization method using a radical polymerization reaction is preferable. As the radical polymerization method, a radical polymerization method (free radical polymerization method) in which a predetermined monomer unit is copolymerized using a polymerization initiator or a reactive silyl group is introduced at a controlled position such as a terminal. Possible controlled radical polymerization methods are mentioned. However, a polymer obtained by a normal free radical polymerization method using an azo compound or a peroxide as a polymerization initiator has a problem that the molecular weight distribution is generally as large as 2 or more and the viscosity is increased. Yes. Therefore, in order to obtain a (meth) acrylate polymer having a narrow molecular weight distribution and a low viscosity and having a crosslinkable functional group at the molecular chain terminal at a high ratio. It is preferable to use a controlled radical polymerization method.

  Examples of the controlled radical polymerization method include a free radical polymerization method and a living radical polymerization method using a chain transfer agent having a specific functional group, and an addition-fragmentation chain transfer (RAFT) polymerization method, Living radical polymerization methods such as a radical polymerization method using a transition metal complex (Transition-Metal-Mediated Living Radical Polymerization) are more preferable. A reaction using a thiol compound having a reactive silyl group and a reaction using a thiol compound having a reactive silyl group and a metallocene compound (Japanese Patent Laid-Open No. 2001-40037) are also suitable.

<Free radical polymerization method>
When using a free radical polymerization method, it is preferable to make it react at 0 to 200 degreeC using a chain transfer agent and an initiator. More preferably, it is particularly preferably set within the range of 25 ° C to 150 ° C. By setting the polymerization reaction temperature within the above range, the reaction can proceed stably without causing runaway. Depending on the activity of the unsaturated group of the polymerizable unsaturated compound to be used, even when a relatively unsaturated acrylate-based polymerizable unsaturated compound is used, when the reaction temperature is less than 0 ° C, The activity is low, the time required to achieve a sufficient polymerization rate is lengthened, and the efficiency is poor. Further, even when a compound having a low polymerization activity such as a styrene type unsaturated compound is used, a sufficient polymerization rate can be achieved under the condition of 25 ° C. or higher. In the case of using the free radical polymerization method, the reaction time can be appropriately set in consideration of the polymerization rate, molecular weight, etc. For example, under the above conditions, the reaction time is usually 1 to 144 hours, preferably It is preferable to set within a range of 2 to 8 hours.

  As the chain transfer agent, known chain transfer agents can be widely used and are not particularly limited. However, a thiol compound is preferable, and a thiol compound having a reactive silyl group is more preferable. For example, mercaptomethyltrimethoxysilane, mercaptomethylmethyldimethoxysilane, mercaptomethyldimethylmethoxysilane, mercaptomethyltriethoxysilane, mercaptomethylmethyldiethoxysilane, mercaptomethyldimethylethoxysilane, mercaptomethyltripropoxysilane, mercaptomethylmethyldisilane Propoxysilane, mercaptomethyldimethylpropoxysilane, 3-mercaptopropyl-trimethoxysilane, 3-mercaptopropyl-triethoxysilane, 3-mercaptopropyl-monomethyldimethoxysilane, 3-mercaptopropyl-monophenyldimethoxysilane, 3-mercaptopropyl -Dimethylmonomethoxysilane, 3-mercaptopropyl-monomethyldiethoxysilane, 4- Rukaputobuchiru - trimethoxysilane and 3-mercaptopropyl butyl - trimethoxysilane. These may be used alone or in combination of two or more.

  The chain transfer agent can be appropriately set in consideration of molecular weight, molecular weight distribution, etc., but can be used in a normal amount, specifically, 100 mol parts of a polymerizable unsaturated compound to be polymerized. The amount is usually 0.001 to 30 mol parts, preferably 0.01 to 20 mol parts.

  The initiator is not particularly limited, and examples thereof include an azo initiator, a peroxide initiator, an ionic initiator, and a redox initiator. These may be used alone or in combination of two or more.

  Examples of the azo initiator include 2,2′-azobis (4-methoxy-2,4-dimethylvaleronitrile) (V-70, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis. (2,4-dimethylvaleronitrile) (V-65, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobisisobutyronitrile (V-60, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis (2-methylbutyronitrile) (V-59, manufactured by Wako Pure Chemical Industries, Ltd.), 1,1′-azobis (cyclohexane-1-carbonitrile) (V-40, Wako Pure) Yakuhin Kogyo Co., Ltd.), 1-[(1-cyano-1-methylethyl) azo] formamide (V-30, Wako Pure Chemical Industries, Ltd.), 2-phenylazo-4-methoxy-2,4 -Dimethyl-valeronitrile (V-19, manufactured by Wako Pure Chemical Industries, Ltd.) Nitrile compound, 2,2′-azobis [2-methyl-N- [1,1-bis (hydroxymethyl) -2-hydroxyethyl] propionamide] (VA-080, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis [2-methyl-N- [1,1-bis (hydroxymethyl) ethyl] propionamide] (VA-082, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis [ 2-methyl-N- [2- (1-hydroxybutyl)]-propionamide] (VA-085, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis [2-methyl-N- (2 -Hydroxyethyl) -propionamide] (VA-086, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis (2-methylpropionamide) dihydrate (VA-088, manufactured by Wako Pure Chemical Industries, Ltd.) ), 2, 2'- Zobis [N- (2-propenyl) -2-methylpropionamide] (VF-096, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis (N-butyl-2-methylpropionamide) (VAm -110, manufactured by Wako Pure Chemical Industries, Ltd.), azoamide compounds such as 2,2′-azobis (N-cyclohexyl-2-methylpropionamide) (VAm-111, manufactured by Wako Pure Chemical Industries, Ltd.), 2 2,2′-azobis (2,4,4-trimethylpentane) (VR-110, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis (2-methylpropane) (VR-160, Wako Pure Chemical) And alkylazo compounds such as those manufactured by Kogyo Co., Ltd.

  Examples of the peroxide initiator include methyl ethyl ketone peroxide (Permec H, manufactured by NOF Corporation), cyclohexanone peroxide species (Perhexa H, manufactured by NOF Corporation), methylcyclohexanone peroxide (Perhexa Q). , Manufactured by NOF Corporation), methylacetoacetate peroxide (Percure SA, manufactured by NOF Corporation), ketone peroxides such as acetylacetone peroxide (Percure A, manufactured by NOF Corporation), 1,1 -Bis (t-hexylperoxy) 3,3,5-trimethylcyclohexane (Perhexa TMH, manufactured by NOF Corporation), 1,1-bis (t-hexylperoxy) cyclohexane (Perhexa HC, NOF Corporation ), 1,1-bis (t-butylperoxy) 3,3,5-trimethylcyclohexane 3M, manufactured by NOF Corporation, 1,1-bis (t-butylperoxy) cyclohexane (Perhexa C, manufactured by NOF Corporation), 1,1-bis (t-butylperoxy) cyclododecane (Perhexa CD-R, manufactured by NOF Corporation), 2,2′-bis (t-butylperoxy) butane (Perhexa 22, manufactured by NOF Corporation), n-butyl 4,4-bis (t -Butylperoxy) valerate) Perhexa V, manufactured by NOF Corporation), 2,2-bis (4,4-di-t-butylperoxycyclohexyl) propane (Pertetra A, manufactured by NOF Corporation), etc. Peroxyketals, t-butyl hydroperoxide (Perbutyl H-69, manufactured by NOF Corporation), p-menthane hydroperoxide (Permenta H, manufactured by NOF Corporation), diisopropylbenzene hydroperoxide ( Pa Cumyl P, manufactured by NOF Corporation, 1,1,3,3-tetramethylbutyl hydroperoxide (Perocta H, manufactured by NOF Corporation), cumene hydroperoxide (Perk Mill H-80, NOF Corporation) Co., Ltd.), hydroperoxides such as t-hexyl hydroperoxide (Perhexyl H, manufactured by NOF Corporation), 2,5-dimethyl-2,5-bis (t-butylperoxy) hexyne-3 (Perhexin 25B, manufactured by NOF Corporation), di-t-butyl peroxide (Perbutyl DR, manufactured by NOF Corporation), t-butyl cumyl peroxy species (Perbutyl C, manufactured by NOF Corporation) ), 2,5-dimethyl-2,5-bis (t-butylperoxy) hexane (Perhexa 25B, manufactured by NOF Corporation), Dicumyl Peroxy species (Park Mill DR, manufactured by NOF Corporation), α, α'-bis (t-bu Dialkyl peroxides such as luperoxy) diisopropylbenzene (Perbutyl P, manufactured by NOF Corporation), octanoyl peroxy species (Perroyl O, manufactured by NOF Corporation), lauroyl peroxy species (Perroyl L, NOF Corporation) Co., Ltd.), stearoyl peroxy species (Perroyl S, manufactured by NOF Corporation), succinic acid peroxy species (Perloyl SA, manufactured by NOF Corporation), benzoyl peroxide (Nyper BW, NOF Corporation) )), Isobutyryl peroxide (Perroyl IB, manufactured by NOF Corporation), 2,4-dichlorobenzoyl peroxy species (Nyper CS, manufactured by NOF Corporation), 3,5,5-trimethylhexanoyl Diacyl peroxides such as peroxy species (Perroyl 355, manufactured by NOF Corporation), di-n-propyl peroxydicarbonate (Perroyl) NPP-50M, manufactured by NOF Corporation), diisopropyl peroxydicarbonate (Perroyl IPP-50, manufactured by NOF Corporation), bis (4-t-butylcyclohexyl) peroxydicarbonate (Perloyl TCP, NOF Corporation) ), Di-2-ethoxyethyl peroxydicarbonate (Perroyl EEP, manufactured by NOF Corporation), di-2-ethoxyhexyl peroxydicarbonate (Perloyl OPP, manufactured by NOF Corporation), Di-2-methoxybutyl peroxydicarbonate (Perroyl MBP, manufactured by NOF Corporation), di (3-methyl-3-methoxybutyl) peroxydicarbonate (Perloyl SOP, manufactured by NOF Corporation), etc. Peroxydicarbonates, α, α'-bis (neodecanoylperoxy) diisopropylbenzene (Nyper ND-R, JP Fatty Co., Ltd.), cumyl peroxyneodecanoate (Park Mill ND-R, manufactured by NOF Corporation), 1,1,3,3-tetramethylbutyl peroxyneodecanoate (Perocta ND-R) , Manufactured by NOF Corporation), 1-cyclohexyl-1-methylethylperoxyneodecanoate (percyclo ND-R, manufactured by NOF Corporation), t-hexylperoxyneodecanoate (perhexyl ND-) R, manufactured by NOF Corporation), t-butyl peroxyneodecanoate (perbutyl ND-R, manufactured by NOF Corporation), t-hexyl peroxypivalate (perhexyl PV, manufactured by NOF Corporation) ), T-butyl peroxypivalate (Perbutyl PV, manufactured by NOF Corporation), 1,1,3,3-tetramethylbutylperoxy-2-ethylhexanoate (Perocta O, NOF Corporation) Made) 2,5-dimethyl-2,5-bis (2-ethylhexanoylperoxy) hexane (Perhexa 250, manufactured by NOF Corporation), 1-cyclohexyl-1-methylethylperoxy-2-ethylhexanoate (Percyclo O, manufactured by NOF Corporation), t-hexyl peroxy-2-ethylhexanoate (Perhexyl O, manufactured by NOF Corporation), t-butyl peroxy-2-ethylhexanoate (perbutyl) O, manufactured by NOF Corporation), t-butyl peroxyisobutyrate (Perbutyl IB, manufactured by NOF Corporation), t-hexyl peroxyisopropyl monocarbonate (Perhexyl I, manufactured by NOF Corporation), t-butyl peroxymaleic acid (Perbutyl MA, manufactured by NOF Corporation), t-butylperoxy 3,5,5-trimethylhexanoate (Perbuthi 355, manufactured by NOF Corporation), t-butyl peroxylaurate (Perbutyl L, manufactured by NOF Corporation), 2,5-dimethyl-2,5-bis (m-toluoylperoxy) hexane ( Perhexa 25MT, manufactured by NOF Corporation, t-butyl peroxyisopropyl monocarbonate (Perbutyl I, manufactured by NOF Corporation), t-butyl peroxy-2-ethylhexyl monocarbonate (Perbutyl E, NOF Corporation) )), T-hexyl peroxybenzoate (Perhexyl Z, manufactured by NOF Corporation), 2,5-dimethyl-2,5-bis (benzoylperoxy) hexane (Perhexa 25Z, manufactured by NOF Corporation) T-butyl peroxyacetate (Perbutyl A, manufactured by NOF Corporation), t-butyl peroxy-m-toluoyl benzoate (Perbutyl ZT, manufactured by NOF Corporation) Peroxyesters such as t-butyl peroxybenzoate (Perbutyl Z, manufactured by NOF Corporation), bis (t-butylperoxy) isophthalate (Perbutyl IF, manufactured by NOF Corporation), t-butyl Peroxyallyl monocarbonate (Peromer AC, manufactured by NOF Corporation), t-butyltrimethylsilyl peroxide (Perbutyl SM, manufactured by NOF Corporation), 3,3′-4,4′-tetra (t-butyl) Peroxycarbonyl) benzophenone (BTTB-50, manufactured by NOF Corporation), 2,3-dimethyl-2,3-diphenylbutane (NOFMER BC, manufactured by NOF Corporation) and the like.

  Examples of the ionic initiator include 2,2′-azobis [2- (phenylamidino) propane] dihydrochloride (VA-545, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis {2 -[N- (4-chlorophenyl) amidino] propane} dihydrochloride (VA-546, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis {2- [N- (4-hydroxyphenyl) amidino] Propane} dihydrochloride (VA-548, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis [2- (N-benzylamidino) propane] dihydrochloride (VA-552, Wako Pure Chemical Industries, Ltd.) 2,2′-azobis [2- (N-allylamidino) propane] dihydrochloride (VA-553, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis (2-amidinop) Pan) dihydrochloride (VA-50, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis {2- [N- (4-hydroxyethyl) amidino] propane} dihydrochloride (VA-558, Wako Pure) Yakuhin Kogyo Co., Ltd.), 2,2′-azobis [2- (5-methyl-2-imidazolin-2-yl) propane] dihydrochloride (VA-041, manufactured by Wako Pure Chemical Industries, Ltd.), 2 , 2'-azobis [2- (2-imidazolin-2-yl) propane] dihydrochloride (VA-044, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2'-azobis [2- (4,5, 6,7-tetrahydro-1H-1,3-diazepin-2-yl) propane] dihydrochloride (VA-054, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis [2- (3,4) , 5,6-Tetrahydropyrimidine 2-yl) propane] dihydrochloride (VA-058, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2'-azobis [2- (5-hydroxy-3,4,5,6-tetrahydropyrimidine-2- Yl) propane] dihydrochloride (VA-059, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis {2- [1- (2-hydroxyethyl) -2-imidazolin-2-yl] propane} Dihydrochloride (VA-060, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis [2- (2-imidazolin-2-yl) propane] (VA-061, manufactured by Wako Pure Chemical Industries, Ltd.) And anionic initiators such as potassium persulfate (KPS, manufactured by Wako Pure Chemical Industries, Ltd.) and ammonium persulfate (APS, manufactured by Wako Pure Chemical Industries, Ltd.).

  Such redox initiators include, for example, systems based on organic peroxides and tertiary amines, such as systems based on benzoyl peroxide and dimethylaniline; and systems based on organic hydroperoxides and transition metals, such as cumene hydroperoxide. And systems based on cobalt naphthate.

  The initiator can be appropriately set in consideration of molecular weight, molecular weight distribution, etc., but can be used in a normal amount, specifically, in 100 mol parts of the polymerizable unsaturated compound to be polymerized. On the other hand, it is usually used in an amount of 0.001 to 30 mol parts, preferably 0.01 to 20 mol parts.

<Addition-cleavage transfer reaction polymerization method>
When the addition-cleavage transfer reaction polymerization method is used, it is preferable to react at 0 ° C. to 200 ° C. using a chain transfer agent and an initiator. More preferably, it is particularly preferably set within the range of 25 ° C to 150 ° C. By setting the polymerization reaction temperature within the above range, the reaction can proceed stably without causing runaway. Depending on the activity of the unsaturated group of the polymerizable unsaturated compound to be used, even when a relatively unsaturated acrylate-based polymerizable unsaturated compound is used, when the reaction temperature is less than 0 ° C, The activity is low, the time required to achieve a sufficient polymerization rate is lengthened, and the efficiency is poor. Further, even when a compound having a low polymerization activity such as a styrene type unsaturated compound is used, a sufficient polymerization rate can be achieved under the condition of 25 ° C. or higher. In the case of using the addition-cleavage transfer reaction polymerization method, the reaction time can be appropriately set in consideration of the polymerization rate, molecular weight, etc. For example, under the above conditions, the reaction time is usually 30 minutes to 144. It is preferable to set the time, preferably within the range of 1 to 24 hours.

  Examples of the chain transfer agent include benzoyl-1-pyrrolecarbodithioate, benzoyldithiobenzoate, cyanoisopropyldithiobenzoate, cumyldithiobenzoate, methoxycarbonylphenylmethyldithiobenzoate, cyanobenzyldithiobenzoate, 1-phenylethyldithiobenzoate T-butyldithiobenzoate S- (thiobenzyl) thioglycolic acid, 1-phenylethylphenyldithiobenzoate, 3-benzylsulfanylthiocarbonylsulfanyl-propionic acid, 2- (benzylsulfanylthiocarbonylsulfanyl) ethanol, 3-benzylsulfanylthio Carbonylsulfanylpropionic acid, S- (1-ethoxycarbonylethyl) O-ethylxanthate, ethyl -2- (2-trifluoroethoxythiocarbonylsulfanyl) propionate, ethyl-2- (1-diethoxyphosphonyl-2,2,2-trifluoroethoxythiocarbonylsulfanyl) propionate, bisthiobenzoyl disulfide, bis (2 , 6-Dimethylthiobenzoyl) disulfide, bis (2,4-dimethylthiobenzoyl) disulfide, bis (4-methoxythiobenzoyl) disulfide, bis (2,4dimethoxythiobenzoyl) disulfide, bis (4-fluorothiobenzoyl) Disulfide, bis (2,4-difluorothiobenzoyl) disulfide, bis (4-cyanothiobenzoyl) disulfide, bis (3,5-dicyanothiobenzoyl) disulfide, bis (3,5-bis (trifluoromethyl) ) Dithiobenzoate) disulfide, bis (2,3,4,5,6-pentafluorothiobenzoyl) disulfide, bis (4-phenylthiobenzoyl) disulfide, bis (2-naphthylthionyl) disulfide, bis (1-naphthyl) Thionyl) disulfide, triphenylmethyldithioisonicotinate, 2-cyanoisopropyl (2,6-dimethyl) dithiobenzoate, 2-cyanoisopropyl (2,4-dimethyl) dithiobenzoate, 2-cyanoisopropyl (4-methoxy) Dithiobenzoate, 2-cyanoisopropyl (2,4-dimethoxy) dithiobenzoate, 2-cyanoisopropyl (4-fluoro) dithiobenzoate, 2-cyanoisopropyl (2,4-difluoro) dithiobenzoate, 2-cyanoisopro Pyrdithioisonicotinate, 2-cyanoisopropyl 4-cyanodithiobenzoate, 2-cyanoisopropyl 3,5-dicyanodithiobenzoate, 2-cyanoisopropyl 3,5-bis (trifluoromethyl) dithiobenzoate, 2-cyanoisopropyl 2 , 3,4,5,6-pentafluorodithiobenzoate, 2-cyanoisopropyl 4-pyridinium dithiocarboxyate 4-toluenesulfonate salt, 2-cyanoisopropyl (4-phenyl) dithiobenzoate, 2-cyanoisopropyl-2 -Naphthyl dithiolate, 2-cyanoisopropyl-1-naphthyl dithiolate, 2-cyano-4-methylpent-2-yldithiobenzoate, 2-cyano-4-methylpent-2-yl-4-cyanodithiobenzoate, - cyano-4-methylpent-2-yl 3,5-bis-trifluoromethyl dithiobenzoate, 2-cyano-4-methylpent-2-yl-4-methoxy-phenyl dithio benzoate. These may be used alone or in combination of two or more.

  The chain transfer agent can be appropriately set in consideration of molecular weight, molecular weight distribution, etc., but can be used in a normal amount, specifically, 100 mol parts of a polymerizable unsaturated compound to be polymerized. The amount is usually 0.001 to 30 mol parts, preferably 0.01 to 20 mol parts.

  The initiator is not particularly limited, and examples thereof include an azo initiator, a peroxide initiator, and an ionic initiator. These may be used alone or in combination of two or more.

  Examples of the azo initiator include 2,2′-azobis (4-methoxy-2,4-dimethylvaleronitrile) (V-70, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis. (2,4-dimethylvaleronitrile) (V-65, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobisisobutyronitrile (V-60, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis (2-methylbutyronitrile) (V-59, manufactured by Wako Pure Chemical Industries, Ltd.), 1,1′-azobis (cyclohexane-1-carbonitrile) (V-40, Wako Pure) Yakuhin Kogyo Co., Ltd.), 1-[(1-cyano-1-methylethyl) azo] formamide (V-30, Wako Pure Chemical Industries, Ltd.), 2-phenylazo-4-methoxy-2,4 -Dimethyl-valeronitrile (V-19, manufactured by Wako Pure Chemical Industries, Ltd.) Nitrile compound, 2,2′-azobis [2-methyl-N- [1,1-bis (hydroxymethyl) -2-hydroxyethyl] propionamide] (VA-080, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis [2-methyl-N- [1,1-bis (hydroxymethyl) ethyl] propionamide] (VA-082, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis [ 2-methyl-N- [2- (1-hydroxybutyl)]-propionamide] (VA-085, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis [2-methyl-N- (2 -Hydroxyethyl) -propionamide] (VA-086, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis (2-methylpropionamide) dihydrate (VA-088, manufactured by Wako Pure Chemical Industries, Ltd.) ), 2, 2'- Zobis [N- (2-propenyl) -2-methylpropionamide] (VF-096, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis (N-butyl-2-methylpropionamide) (VAm -110, manufactured by Wako Pure Chemical Industries, Ltd.), azoamide compounds such as 2,2′-azobis (N-cyclohexyl-2-methylpropionamide) (VAm-111, manufactured by Wako Pure Chemical Industries, Ltd.), 2 2,2′-azobis (2,4,4-trimethylpentane) (VR-110, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis (2-methylpropane) (VR-160, Wako Pure Chemical) And alkylazo compounds such as those manufactured by Kogyo Co., Ltd.

  Examples of the peroxide initiator include methyl ethyl ketone peroxide (Permec H, manufactured by NOF Corporation), cyclohexanone peroxide species (Perhexa H, manufactured by NOF Corporation), methylcyclohexanone peroxide (Perhexa Q). , Manufactured by NOF Corporation), methylacetoacetate peroxide (Percure SA, manufactured by NOF Corporation), ketone peroxides such as acetylacetone peroxide (Percure A, manufactured by NOF Corporation), 1,1 -Bis (t-hexylperoxy) 3,3,5-trimethylcyclohexane (Perhexa TMH, manufactured by NOF Corporation), 1,1-bis (t-hexylperoxy) cyclohexane (Perhexa HC, NOF Corporation ), 1,1-bis (t-butylperoxy) 3,3,5-trimethylcyclohexane 3M, manufactured by NOF Corporation, 1,1-bis (t-butylperoxy) cyclohexane (Perhexa C, manufactured by NOF Corporation), 1,1-bis (t-butylperoxy) cyclododecane (Perhexa CD-R, manufactured by NOF Corporation), 2,2′-bis (t-butylperoxy) butane (Perhexa 22, manufactured by NOF Corporation), n-butyl 4,4-bis (t -Butylperoxy) valerate) Perhexa V, manufactured by NOF Corporation), 2,2-bis (4,4-di-t-butylperoxycyclohexyl) propane (Pertetra A, manufactured by NOF Corporation), etc. Peroxyketals, t-butyl hydroperoxide (Perbutyl H-69, manufactured by NOF Corporation), p-menthane hydroperoxide (Permenta H, manufactured by NOF Corporation), diisopropylbenzene hydroperoxide ( Pa Cumyl P, manufactured by NOF Corporation, 1,1,3,3-tetramethylbutyl hydroperoxide (Perocta H, manufactured by NOF Corporation), cumene hydroperoxide (Perk Mill H-80, NOF Corporation) Co., Ltd.), hydroperoxides such as t-hexyl hydroperoxide (Perhexyl H, manufactured by NOF Corporation), 2,5-dimethyl-2,5-bis (t-butylperoxy) hexyne-3 (Perhexin 25B, manufactured by NOF Corporation), di-t-butyl peroxide (Perbutyl DR, manufactured by NOF Corporation), t-butyl cumyl peroxy species (Perbutyl C, manufactured by NOF Corporation) ), 2,5-dimethyl-2,5-bis (t-butylperoxy) hexane (Perhexa 25B, manufactured by NOF Corporation), Dicumyl Peroxy species (Park Mill DR, manufactured by NOF Corporation), α, α'-bis (t-bu Dialkyl peroxides such as luperoxy) diisopropylbenzene (Perbutyl P, manufactured by NOF Corporation), octanoyl peroxy species (Perroyl O, manufactured by NOF Corporation), lauroyl peroxy species (Perroyl L, NOF Corporation) Co., Ltd.), stearoyl peroxy species (Perroyl S, manufactured by NOF Corporation), succinic acid peroxy species (Perloyl SA, manufactured by NOF Corporation), benzoyl peroxide (Nyper BW, NOF Corporation) )), Isobutyryl peroxide (Perroyl IB, manufactured by NOF Corporation), 2,4-dichlorobenzoyl peroxy species (Nyper CS, manufactured by NOF Corporation), 3,5,5-trimethylhexanoyl Diacyl peroxides such as peroxy species (Perroyl 355, manufactured by NOF Corporation), di-n-propyl peroxydicarbonate (Perroyl) NPP-50M, manufactured by NOF Corporation), diisopropyl peroxydicarbonate (Perroyl IPP-50, manufactured by NOF Corporation), bis (4-t-butylcyclohexyl) peroxydicarbonate (Perloyl TCP, NOF Corporation) ), Di-2-ethoxyethyl peroxydicarbonate (Perroyl EEP, manufactured by NOF Corporation), di-2-ethoxyhexyl peroxydicarbonate (Perloyl OPP, manufactured by NOF Corporation), Di-2-methoxybutyl peroxydicarbonate (Perroyl MBP, manufactured by NOF Corporation), di (3-methyl-3-methoxybutyl) peroxydicarbonate (Perloyl SOP, manufactured by NOF Corporation), etc. Peroxydicarbonates, α, α'-bis (neodecanoylperoxy) diisopropylbenzene (Nyper ND-R, JP Fatty Co., Ltd.), cumyl peroxyneodecanoate (Park Mill ND-R, manufactured by NOF Corporation), 1,1,3,3-tetramethylbutyl peroxyneodecanoate (Perocta ND-R) , Manufactured by NOF Corporation), 1-cyclohexyl-1-methylethylperoxyneodecanoate (percyclo ND-R, manufactured by NOF Corporation), t-hexylperoxyneodecanoate (perhexyl ND-) R, manufactured by NOF Corporation), t-butyl peroxyneodecanoate (perbutyl ND-R, manufactured by NOF Corporation), t-hexyl peroxypivalate (perhexyl PV, manufactured by NOF Corporation) ), T-butyl peroxypivalate (Perbutyl PV, manufactured by NOF Corporation), 1,1,3,3-tetramethylbutylperoxy-2-ethylhexanoate (Perocta O, NOF Corporation) Made) 2,5-dimethyl-2,5-bis (2-ethylhexanoylperoxy) hexane (Perhexa 250, manufactured by NOF Corporation), 1-cyclohexyl-1-methylethylperoxy-2-ethylhexanoate (Percyclo O, manufactured by NOF Corporation), t-hexyl peroxy-2-ethylhexanoate (Perhexyl O, manufactured by NOF Corporation), t-butyl peroxy-2-ethylhexanoate (perbutyl) O, manufactured by NOF Corporation), t-butyl peroxyisobutyrate (Perbutyl IB, manufactured by NOF Corporation), t-hexyl peroxyisopropyl monocarbonate (Perhexyl I, manufactured by NOF Corporation), t-butyl peroxymaleic acid (Perbutyl MA, manufactured by NOF Corporation), t-butylperoxy 3,5,5-trimethylhexanoate (Perbuthi 355, manufactured by NOF Corporation), t-butyl peroxylaurate (Perbutyl L, manufactured by NOF Corporation), 2,5-dimethyl-2,5-bis (m-toluoylperoxy) hexane ( Perhexa 25MT, manufactured by NOF Corporation, t-butyl peroxyisopropyl monocarbonate (Perbutyl I, manufactured by NOF Corporation), t-butyl peroxy-2-ethylhexyl monocarbonate (Perbutyl E, NOF Corporation) )), T-hexyl peroxybenzoate (Perhexyl Z, manufactured by NOF Corporation), 2,5-dimethyl-2,5-bis (benzoylperoxy) hexane (Perhexa 25Z, manufactured by NOF Corporation) T-butyl peroxyacetate (Perbutyl A, manufactured by NOF Corporation), t-butyl peroxy-m-toluoyl benzoate (Perbutyl ZT, manufactured by NOF Corporation) Peroxyesters such as t-butyl peroxybenzoate (Perbutyl Z, manufactured by NOF Corporation), bis (t-butylperoxy) isophthalate (Perbutyl IF, manufactured by NOF Corporation), t-butyl Peroxyallyl monocarbonate (Peromer AC, manufactured by NOF Corporation), t-butyltrimethylsilyl peroxide (Perbutyl SM, manufactured by NOF Corporation), 3,3′-4,4′-tetra (t-butyl) Peroxycarbonyl) benzophenone (BTTB-50, manufactured by NOF Corporation), 2,3-dimethyl-2,3-diphenylbutane (NOFMER BC, manufactured by NOF Corporation) and the like.

  Examples of the ionic initiator include 2,2′-azobis [2- (phenylamidino) propane] dihydrochloride (VA-545, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis {2 -[N- (4-chlorophenyl) amidino] propane} dihydrochloride (VA-546, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis {2- [N- (4-hydroxyphenyl) amidino] Propane} dihydrochloride (VA-548, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis [2- (N-benzylamidino) propane] dihydrochloride (VA-552, Wako Pure Chemical Industries, Ltd.) 2,2′-azobis [2- (N-allylamidino) propane] dihydrochloride (VA-553, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis (2-amidinop) Pan) dihydrochloride (VA-50, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis {2- [N- (4-hydroxyethyl) amidino] propane} dihydrochloride (VA-558, Wako Pure) Yakuhin Kogyo Co., Ltd.), 2,2′-azobis [2- (5-methyl-2-imidazolin-2-yl) propane] dihydrochloride (VA-041, manufactured by Wako Pure Chemical Industries, Ltd.), 2 , 2'-azobis [2- (2-imidazolin-2-yl) propane] dihydrochloride (VA-044, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2'-azobis [2- (4,5, 6,7-tetrahydro-1H-1,3-diazepin-2-yl) propane] dihydrochloride (VA-054, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis [2- (3,4) , 5,6-Tetrahydropyrimidine 2-yl) propane] dihydrochloride (VA-058, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2'-azobis [2- (5-hydroxy-3,4,5,6-tetrahydropyrimidine-2- Yl) propane] dihydrochloride (VA-059, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis {2- [1- (2-hydroxyethyl) -2-imidazolin-2-yl] propane} Dihydrochloride (VA-060, manufactured by Wako Pure Chemical Industries, Ltd.), 2,2′-azobis [2- (2-imidazolin-2-yl) propane] (VA-061, manufactured by Wako Pure Chemical Industries, Ltd.) And anionic initiators such as potassium persulfate (KPS, manufactured by Wako Pure Chemical Industries, Ltd.) and ammonium persulfate (APS, manufactured by Wako Pure Chemical Industries, Ltd.).

  The initiator can be appropriately set in consideration of molecular weight, molecular weight distribution, etc., but can be used in a normal amount, specifically, in 100 mol parts of the polymerizable unsaturated compound to be polymerized. On the other hand, it is usually used in an amount of 0.001 to 30 mol parts, preferably 0.01 to 20 mol parts.

<Polymerization method using a thiol compound having a reactive silyl group and a metallocene compound>
It is preferable to use a metallocene compound as a metal catalyst and to react at 0 ° C. to 150 ° C. using a thiol compound having at least one reactive silyl group in the molecule. More preferably, it is particularly preferably set within the range of 25 ° C to 120 ° C. By setting the polymerization reaction temperature within the above range, the reaction can proceed stably without causing runaway. Depending on the activity of the unsaturated group of the polymerizable unsaturated compound to be used, even when a relatively unsaturated acrylate-based polymerizable unsaturated compound is used, when the reaction temperature is less than 0 ° C, The activity is low, the time required to achieve a sufficient polymerization rate is lengthened, and the efficiency is poor. Further, even when a compound having a low polymerization activity such as a styrene type unsaturated compound is used, a sufficient polymerization rate can be achieved under the condition of 25 ° C. or higher. In the case of using the polymerization method, the reaction time can be appropriately set in consideration of the polymerization rate, molecular weight, etc. For example, under the above conditions, the reaction time is usually 1 to 12 hours, preferably 2 It is preferable to set within a range of ˜8 hours.

  The metallocene compound is not particularly limited, and examples thereof include dicyclopentadiene-Ti-dichloride, dicyclopentadiene-Ti-bisphenyl, dicyclopentadiene-Ti-bis-2,3,4,5,6-pentafluoropheny. -1-yl, dicyclopentadiene-Ti-bis-2,3,5,6-tetrafluorophen-1-yl, dicyclopentadiene-Ti-bis-2,5,6-trifluorophen-1-yl Dicyclopentadiene-Ti-bis-2,6-difluorophen-1-yl, dicyclopentadiene-Ti-bis-2,4-difluorophen-1-yl, dimethylcyclopentadienyl-Ti-bis-2 , 3,4,5,6-pentafluorophen-1-yl, dimethylcyclopentadienyl-Ti-bis-2,3 5,6-tetrafluorophen-1-yl, dimethylcyclopentadienyl-Ti-bis-2,6-difluorophen-1-yl, dimethylcyclopentadienyl-Ti-bis-2,6-difluoro-3 Titanocene compounds such as-(pyr-1-yl) -phen-1-yl; dicyclopentadienyl-Zr-dichloride, dicyclopentadiene-Zr-bisphenyl, dicyclopentadiene-Zr-bis-2,3 , 4,5,6-pentafluorophen-1-yl, dicyclopentadiene-Zr-bis-2,3,5,6-tetrafluorophen-1-yl, dicyclopentadiene-Zr-bis-2,5 , 6-trifluorophen-1-yl, dicyclopentadiene-Zr-bis-2,6-difluorophen-1-yl, dicyclopentadiene -Zr-bis-2,4-difluorophen-1-yl, dimethylcyclopentadienyl-Zr-bis-2,3,4,5,6-pentafluorophen-1-yl, dimethylcyclopentadienyl- Zr-bis-2,3,5,6-tetrafluorophen-1-yl, dimethylcyclopentadienyl-Zr-bis-2,6-difluorophen-1-yl, dimethylcyclopentadienyl-Zr-bis Zirconocene compounds such as 2,6-difluoro-3- (pyr-1-yl) -phen-1-yl); dicyclopentadienyl-V-chloride, bismethylcyclopentadienyl-V-chloride, Bispentamethylcyclopentadienyl-V-chloride, dicyclopentadienyl-Ru-chloride, dicyclopentadienyl-Cr-chloro Can be mentioned. These may be used alone or in combination of two or more.

  The metallocene compound can be used in a normal catalytic amount. Specifically, the metallocene compound is usually 0.1 to 0.00001 mol part, preferably 100 to 100 mol part of the polymerizable unsaturated compound to be polymerized, preferably Used in an amount of 0.0001-0.00005 mol parts.

  The thiol compound having a reactive silyl group is not particularly limited. For example, mercaptomethyltrimethoxysilane, mercaptomethylmethyldimethoxysilane, mercaptomethyldimethylmethoxysilane, mercaptomethyltriethoxysilane, mercaptomethylmethyldiethoxysilane, mercapto Methyldimethylethoxysilane, mercaptomethyltripropoxysilane, mercaptomethylmethyldipropoxysilane, mercaptomethyldimethylpropoxysilane, 3-mercaptopropyl-trimethoxysilane, 3-mercaptopropyl-trimethoxysilane, 3-mercaptopropyl-triethoxy Silane, 3-mercaptopropyl-monomethyldimethoxysilane, 3-mercaptopropyl-monophenyldimethoxysila , 3-mercaptopropyl - dimethyl mono silane, 3-mercaptopropyl - monomethyl diethoxy silane, 4-mercaptomethyl-butyl - trimethoxysilane and 3-mercaptopropyl butyl - and tri methoxy silane. These may be used alone or in combination of two or more.

  The amount of the thiol compound having a reactive silyl group can be appropriately set in consideration of the molecular weight of the polymer to be obtained, the polymerization rate, etc., but the reaction proceeds smoothly and does not cause the reaction to run away. The metallocene compound and the thiol compound having a reactive silyl group are usually used in a molar ratio within the range of 100: 1 to 1: 50000, preferably 10: 1 to 1: 10000.

<Radical polymerization using transition metal complex>
When using the radical polymerization method using a transition metal complex, it is preferable to make it react at 0 to 200 degreeC using a transition metal complex, an organic halide, and / or a ligand. More preferably, it is particularly preferably set within the range of 25 ° C to 150 ° C. By setting the polymerization reaction temperature within the above range, the reaction can proceed stably without causing runaway. Depending on the activity of the unsaturated group of the polymerizable unsaturated compound to be used, even when a relatively unsaturated acrylate-based polymerizable unsaturated compound is used, when the reaction temperature is less than 0 ° C, The activity is low, the time required to achieve a sufficient polymerization rate is lengthened, and the efficiency is poor. Further, even when a compound having a low polymerization activity such as a styrene type unsaturated compound is used, a sufficient polymerization rate can be achieved under the condition of 25 ° C. or higher. In the case of using the addition-cleavage transfer reaction polymerization method, the reaction time can be appropriately set in consideration of the polymerization rate, molecular weight, etc. For example, under the above conditions, the reaction time is usually 30 minutes to 144. It is preferable to set the time, preferably within the range of 1 to 24 hours.

It does not specifically limit as said transition metal complex, For example, what is described in WO97 / 18247 can be utilized. Among these, a complex of zero-valent copper, monovalent copper, divalent ruthenium, divalent iron, or divalent nickel is preferable. Of these, a copper complex is preferable. Specific examples of monovalent copper compounds include cuprous chloride, cuprous bromide, cuprous iodide, cuprous cyanide, cuprous oxide, cuprous perchlorate, etc. is there. When using cuprous chloride, cuprous bromide, cuprous iodide, cuprous cyanide, cuprous oxide, cuprous perchlorate, if necessary, zero-valent copper, cuprous chloride Dicopper, cupric bromide, and cupric iodide can also be used.
A tristriphenylphosphine complex of divalent ruthenium chloride (RuCl ₂ (PPh ₃ ) ₃ ) is also suitable as a catalyst. When a ruthenium compound is used as a catalyst, an aluminum alkoxide is added as an activator. Further, a divalent iron bistriphenylphosphine complex (FeCl ₂ (PPh ₃ ) ₂ ), a divalent nickel bistriphenylphosphine complex (NiCl ₂ (PPh ₃ ) ₂ ), and a divalent nickel bistributylphosphine complex (NiBr ₂ (PBu ₃ ) ₂ ) is also suitable as a catalyst.

  When using a copper compound as a catalyst, the ligand described in WO97 / 18247 can be used as the ligand. Although not particularly limited, amine-based ligands are preferable, and bipyridyl compounds such as 2,2′-bipyridyl and its derivatives, 1,10-phenanthroline and its derivatives, hexamethyltriethylenetetraamine, bispicolylamine , Ligands such as aliphatic amines such as trialkylamine, tetramethylethylenediamine, pentamethyldiethylenetriamine, and hexamethyl (2-aminoethyl) amine. In the present invention, among these, polyamine compounds, particularly aliphatic polyamines such as pentamethyldiethylenetriamine and hexamethyl (2-aminoethyl) amine are preferred. Moreover, when using a polyamine compound, a pyridine-type compound, or an aliphatic amine compound as a ligand in the case of using a copper compound as a catalyst, these ligands must have three or more amino groups. Is preferred. The amino group in the present invention represents a group having a nitrogen atom-carbon atom bond, and among these, a group in which a nitrogen atom is bonded only to a carbon atom and / or a hydrogen atom is preferable. The metallocene compounds listed above can also be used.

  The amount of the ligand as described above is determined from the number of coordination sites of the transition metal and the number of groups coordinated by the ligand under the conditions of normal atom transfer radical polymerization, so that they are almost equal. Is set to For example, the amount of 2,2'-bipyridyl and its derivatives added to CuBr is usually twice as much as the molar ratio, and in the case of pentamethyldiethylenetriamine, it is once as high as the molar ratio. In the present invention, when a ligand is added to initiate polymerization, and / or when a catalyst activity is controlled by adding a ligand, there is no particular limitation, but the metal atom is excessive relative to the ligand. Is preferred. The ratio between the coordination position and the coordinating group is preferably 1.2 times or more, more preferably 1.4 times or more, particularly preferably 1.6 times or more, and particularly preferably 2 times or more. It is.

As an initiator, an organic halide, particularly an organic halide having a highly reactive carbon-halogen bond (for example, a carbonyl compound having a halogen at the α-position or a compound having a halogen at the benzyl-position) or a sulfonyl halide is used. Used.
If Specific _{examples, C 6 H 5 -CH 2 X} , C 6 H 5 -C (H) (X) CH 3, C 6 H 5 -C (X) (CH 3) 2, XCH 2 - _{C 6 H 5 -CH 2 X,} XC (H) (CH 3) -C 6 H5-C (H) (CH 3) X ( where in the above _formula, C 6 _{H 5} is a phenyl group, X is chlorine , bromine or ^{_{iodine), R 3 -C (H)}} (X) -CO 2 R 4, R 3 -C (CH 3) (X) -CO 2 R 4, R 3 -C, (H) (X) _{^{-C (O) R 4, R}} 3 -C (CH 3) (X) -C (O) R 4, R 3 -C 6 H 4 -SO 2 X ( ^wherein, R 3, ^{R 4} is a hydrogen atom Or a C1-C20 alkyl group, an aryl group, or an aralkyl group, X is chlorine, a bromine, or an iodine) etc. are mentioned.

  In radical polymerization methods using transition metal complexes, aluminum trial chelates such as triethoxyaluminum, tripropoxyaluminum, triisopropoxyaluminum, tri-n-butoxyaluminum, tri-t-butoxyaluminum, trisec-butoxyaluminum and dioctyltin And divalent tin compounds such as diethylhexyltin and dibutyltin, and organic substances such as glucose and ascorbic acid can be used as additives for activating the polymerization.

  In the synthesis of the (meth) acrylic acid ester polymer, the polymerization can be carried out without solvent or in various solvents. Examples of the solvent include hydrocarbon solvents such as benzene, xylene and toluene, ether solvents such as diethyl ether and tetrahydrofuran, halogenated hydrocarbon solvents such as methylene chloride and chloroform, acetone, methyl ethyl ketone, and methyl isobutyl ketone. Ketone solvents such as methanol, ethanol, propanol, isopropanol, n-butyl alcohol, tert-butyl alcohol, etc., nitrile solvents such as acetonitrile, propionitrile, benzonitrile, ethyl acetate, butyl acetate, etc. Polyoxyalkylene polymers such as ester solvents, carbonate solvents such as ethylene carbonate and propylene carbonate, and the like can be mentioned, and these can be used alone or in admixture of two or more.

  Further, by using a polyoxyalkylene polymer, a saturated hydrocarbon polymer or the like as a solvent, a subsequent degassing step or the like can be eliminated.

  The (meth) acrylic acid ester-based polymer having a crosslinkable silicon group may be used alone or in combination of two or more.

  These organic polymers having a crosslinkable silicon group may be used alone or in combination of two or more. Specifically, it comprises a polyoxyalkylene polymer having a crosslinkable silicon group, a saturated hydrocarbon polymer having a crosslinkable silicon group, and a (meth) acrylic acid ester polymer having a crosslinkable silicon group. An organic polymer obtained by blending two or more selected from the group can also be used.

A method for producing an organic polymer obtained by blending a polyoxyalkylene polymer having a crosslinkable silicon group and a (meth) acrylic acid ester polymer having a crosslinkable silicon group is disclosed in JP-A-59-122541. Although proposed in Japanese Laid-Open Patent Publication No. 63-112642, Japanese Laid-Open Patent Publication No. 6-172631, and Japanese Laid-Open Patent Publication No. 11-116763, the invention is not particularly limited thereto.
Preferable specific examples include a crosslinkable silicon group and a molecular chain substantially having the following general formula (9):
—CH ₂ —C (R ³⁵ ) (COOR ³⁶ ) — (9)
(Wherein R ³⁵ represents a hydrogen atom or a methyl group, and R ³⁶ represents an alkyl group having 1 to 8 carbon atoms) (meth) acrylic acid ester monomer having an alkyl group having 1 to 8 carbon atoms Unit and the following general formula (10):
—CH ₂ —C (R ³⁵ ) (COOR ³⁷ ) — (10)
(Wherein R ³⁵ is the same as described above, and R ³⁷ represents an alkyl group having 10 or more carbon atoms) and is a copolymer comprising a (meth) acrylic acid ester monomer unit having an alkyl group having 10 or more carbon atoms. In this method, a polymer is blended with a polyoxyalkylene polymer having a crosslinkable silicon group.

As R ³⁶ of the general formula (9), for example, a methyl group, an ethyl group, a propyl group, an n-butyl group, a t-butyl group, a 2-ethylhexyl group and the like are 1 to 8, preferably 1 to 4, More preferably, 1-2 alkyl groups are mentioned. The alkyl group of R ³⁶ may alone, or may be a mixture of two or more.

R ^{37 in the} general formula (10) is, for example, a long-chain alkyl having 10 or more carbon atoms such as lauryl group, tridecyl group, cetyl group, stearyl group, behenyl group, etc., usually 10-30, preferably 10-20. Group. Incidentally, as with the alkyl group for R ³⁷ is the R ^36, alone may be, or may be a mixture of two or more.

  The molecular chain of the (meth) acrylic acid ester copolymer is substantially composed of monomer units of the formula (9) and the formula (10), and the term “substantially” here means the copolymer. It means that the total of the monomer units of the formula (9) and the formula (10) present therein exceeds 50% by mass. The total of the monomer units of the formula (9) and the formula (10) is preferably 70% by mass or more.

  Further, the abundance ratio of the monomer unit of the formula (9) and the monomer unit of the formula (10) is preferably 95: 5 to 40:60, and more preferably 90:10 to 60:40 by mass ratio.

  Examples of monomer units other than the formulas (9) and (10) that may be contained in the copolymer (hereinafter also referred to as other monomer units) include α such as acrylic acid and methacrylic acid. , Β-unsaturated carboxylic acids; amide groups such as acrylamide, methacrylamide, N-methylol acrylamide, N-methylol methacrylamide, epoxy groups such as glycidyl acrylate, glycidyl methacrylate, diethylaminoethyl acrylate, diethylaminoethyl methacrylate, aminoethyl vinyl ether, etc. And other monomer units derived from acrylonitrile, styrene, α-methylstyrene, alkyl vinyl ether, vinyl chloride, vinyl acetate, vinyl propionate, ethylene and the like.

  Having a crosslinkable silicon group used in a method for producing an organic polymer obtained by blending a polyoxyalkylene polymer having a crosslinkable silicon group and a (meth) acrylic acid ester polymer having a crosslinkable silicon group (meta ) Other preferred specific examples of the acrylate polymer include, for example, (a1) a methyl (meth) acrylate monomer unit as disclosed in JP-A-2008-44975, and (a2) An acrylic polymer having a crosslinkable silicon group containing a (meth) acrylic acid alkyl ester monomer unit having an alkyl group having 8 carbon atoms.

The molecular chain of the acrylic copolymer preferably contains a total of 50% by mass or more of the monomer unit (a1) and the monomer unit (a2). It is more preferable that the total of the monomer units is 70% by mass or more. The abundance ratio of (a1) to (a2) is preferably (a1) / (a2) = 90/10 to 20/80, more preferably 70/30 to 30/70 in terms of mass ratio. When the mass ratio of (a1) / (a2) is in the range of 90/10 to 20/80, the transparency can be improved.
The acrylic copolymer may contain monomer units other than (a1) and (a2). As the monomer unit other than (a1) and (a2), for example, the other monomer units described above in the description of the (meth) acrylic acid ester-based copolymer can be used in the same manner.

600-5000 are preferable and, as for the number average molecular weight of the said acrylic copolymer, 1000-4500 are more preferable. By setting the number average molecular weight within this range, compatibility with the polyoxyalkylene polymer having a crosslinkable silicon group can be improved.
The acrylic copolymer is preferably used in an amount of 5 to 900 parts by mass with respect to 100 parts by mass of the polyoxyalkylene polymer having a crosslinkable silicon group. These acrylic copolymers may be used alone or in combination of two or more.

  Organic polymers formed by blending a saturated hydrocarbon polymer having a crosslinkable silicon group and a (meth) acrylic acid ester copolymer having a crosslinkable silicon group are disclosed in JP-A-1-168774 and JP-A-2000-. Although it is proposed in Japanese Patent No. 186176, etc., it is not particularly limited thereto.

  Furthermore, as a method for producing an organic polymer obtained by blending a (meth) acrylic acid ester copolymer having a crosslinkable silicon group, in the presence of an organic polymer having a crosslinkable silicon group ( A method of polymerizing a meth) acrylate monomer can be used. This production method is specifically disclosed in JP-A-59-78223, JP-A-59-168014, JP-A-60-228516, JP-A-60-228517, etc. It is not limited to these.

  When blending two or more kinds of polymers, a saturated hydrocarbon polymer having a crosslinkable silicon group and / or a crosslink with respect to 100 parts by mass of a polyoxyalkylene polymer having a crosslinkable silicon group. It is preferable to use 10-200 mass parts of the (meth) acrylic acid ester-type polymer which has a crystalline silicon group, and it is more preferable to use 20-80 mass parts.

  The (B) silane compound comprises an epoxy silane compound represented by the following formula (1) and an amino silane compound represented by the following formula (2). It is a silane compound obtained by reacting in the range of 10 mol.

In Formula (1), R ^{1 to} R ³ are each a hydrogen atom or an alkyl group, preferably a hydrogen atom, a methyl group, an ethyl group, or a propyl group, and more preferably a hydrogen atom. R ⁴ is an alkylene group or an alkyleneoxyalkylene group, and is a methylene group, ethylene group, propylene group, butylene group, pentylene group, hexylene group, heptylene group, octylene group, methyleneoxyethylene group, methyleneoxypropylene group, methyleneoxybutylene. Group, ethyleneoxyethylene group and ethyleneoxypropylene group are preferable, butylene group, octylene group and methyleneoxypropylene group are more preferable. R ⁵ is a monovalent hydrocarbon group, preferably an alkyl group such as a methyl group, an ethyl group or a propyl group; an alkenyl group such as a vinyl group, an allyl group or a butenyl group; an aryl group such as a phenyl group or a tolyl group; Groups are more preferred. When a plurality of R ⁵ are present, they may be the same or different. R ⁶ is an alkyl group, preferably a methyl group, an ethyl group, or a propyl group, and more preferably a methyl group or an ethyl group. When a plurality of R ⁶ are present, they may be the same or different. a is 0, 1 or 2, and 0 is preferable.

In the formula (2), R ^{7 to} R ¹² are each a hydrogen atom or an alkyl group, preferably a hydrogen atom, a methyl group, an ethyl group, or a propyl group, and more preferably a hydrogen atom. R ¹³ is a monovalent hydrocarbon group, preferably an alkyl group or an alkoxy group, more preferably a methyl group, an ethyl group, a propyl group, a methoxy group, an ethoxy group, or a propoxy group, and even more preferably a methoxy group or an ethoxy group. R ¹⁴ is an alkyl group, preferably a methyl group, an ethyl group, or a propyl group, and more preferably a methyl group or an ethyl group. b is 0 or 1. (3-b) pieces of R ¹⁴ may be the same or different.

  Examples of the epoxysilane compound include 4-oxiranylbutyltrimethoxysilane, 8-oxiranyloctyltrimethoxysilane, 3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropylmethyldimethoxysilane, 3 -Glycidoxypropyl triethoxysilane etc. are mentioned.

  Examples of the aminosilane compound include 3-aminopropyltrimethoxysilane, 3-aminopropyltriethoxysilane, 3-aminopropylmethyldimethoxysilane, 3-aminopropylmethyldiethoxysilane, and the like.

The reaction condition between the epoxysilane compound and the aminosilane compound is that the primary amino group of the aminosilane compound reacts with the epoxysilane compound, the primary amino group becomes a secondary amino group or a tertiary amino group, What is necessary is just to make it react so that a primary amino group may not remain | survive.
As the reaction conditions for that purpose, for example, the aminosilane compound and the epoxysilane compound are mixed in the presence or absence of a solvent, and 25 ° C to 100 ° C, preferably 30 ° C to 90 ° C, more preferably 40 ° C. It is suitable to make it react at the reaction temperature of -80 degreeC. By setting the reaction temperature within the above range, the reaction can proceed stably without causing runaway. When the reaction temperature is less than 25 ° C., the activity is low, the time required to achieve a sufficient reaction is lengthened, and the efficiency is poor. The reaction time can be appropriately set in consideration of the reaction temperature and the like. For example, under the above conditions, the reaction time is usually 1 to 336 hours, preferably 24 to 72 hours. Is preferred.
The reaction ratio (molar ratio) of the epoxysilane compound and the aminosilane compound is 1.5 to 10 mol, preferably 1.6 to 5.0 mol, more preferably 1.7 mol of the epoxysilane compound with respect to 1 mol of the aminosilane compound. It is made to react so that it may become -2.4 mol.

The epoxy silane compound and the aminosilane compound are reacted by heating at a reaction temperature of preferably 40 ° C. or higher, more preferably 40 to 100 ° C., and even more preferably 40 to 80 ° C. Is cleaved and cyclized by an alcohol exchange reaction between the hydroxyl group produced by this reaction and the alkoxy group in the aminosilane compound, whereby a carbacyltolane derivative represented by the following formula (11) can be obtained. The carbacyltolane derivative represented by the following formula (11) is a compound having a peak from −60 ppm to −70 ppm in ²⁹ Si-NMR.

In the formula (11), R ^{1 to} R ⁶ and a are the same as the formula (1), R ^{7 to} R ¹² are the same as the formula (2), and b in the formula (2) is When 0, R ¹⁵ is the same as OR ^{14 in the} formula (2), and when b in the formula (2) is 1, R ¹⁵ is the same as R ^{13 in the} formula (2). The alkoxy group bonded to the silicon atom may be partially substituted by an alcohol exchange reaction. The silicon atom-bonded alkoxy group of the raw material and the silicon atom-bonded alkoxy group in the carbacyltran derivative generated by the reaction May not be the same.

  The blending ratio of the (B) silane compound is a blend of 0.1 to 40 parts by mass of the (B) silane compound with respect to 100 parts by mass of the (A) organic polymer. It is preferable to mix | blend a mass part, and it is more preferable to mix | blend 0.5-20 mass parts. The (B) silane compound may be used alone or in combination of two or more.

  The (C) titanium catalyst is at least one selected from the group consisting of a titanium chelate represented by the following formula (3) and a titanium chelate represented by the following formula (4).

In the formula (3), n R ^{21 s} are each independently a substituted or unsubstituted hydrocarbon group having 1 to 20 carbon atoms, and 4-n R ^{22 s} are each independently a hydrogen atom or A substituted or unsubstituted hydrocarbon group having 1 to 20 carbon atoms, wherein 4-n R ²³ and 4-n R ²⁴ are each independently substituted or unsubstituted C 1-20 carbon atoms. A hydrocarbon group and n is 0, 1, 2 or 3;

In the formula (4), R ²⁵ is a substituted or unsubstituted divalent hydrocarbon group having 1 to 20 carbon atoms, and the two R ²⁶ are independently hydrogen atoms or substituted or unsubstituted. It is a hydrocarbon group having 1 to 20 carbon atoms, and two R ²⁷ and two R ²⁸ are each independently a substituted or unsubstituted hydrocarbon group having 1 to 20 carbon atoms.

  Examples of the titanium chelate represented by the formula (3) or the formula (4) include titanium dimethoxide bis (ethyl acetoacetate), titanium diethoxide bis (ethyl acetoacetate), and titanium diisopropoxide bis (ethyl). Acetoacetate), titanium diisopropoxide bis (methyl acetoacetate), titanium diisopropoxide bis (t-butyl acetoacetate), titanium diisopropoxide bis (methyl-3-oxo-4,4-dimethylhexano) Acid), titanium diisopropoxide bis (ethyl-3-oxo-4,4,4-trifluorobutanoate), titanium di-n-butoxide bis (ethyl acetoacetate), titanium diisobutoxide bis (ethyl acetoacetate) ), Titanium di-t-butoxide bis (ethyl acetoacetate), Titanium di-2-ethylhexoxide bis (ethyl acetoacetate), Titanium bis (1-methoxy-2-propoxide) bis (ethyl acetoacetate), Titanium bis ( 3-oxo-2-butoxide) bis (ethyl acetoacetate), titanium bis (3-diethylaminopropoxide) bis (ethyl acetoacetate), titanium triisopropoxide (ethyl acetoacetate), titanium triisopropoxide (allyl acetoacetate) Acetate), titanium triisopropoxide (methacryloxyethyl acetoacetate), 1,2-dioxyethane titanium bis (ethylacetoacetate), 1,3-dioxypropane titanium bis (ethylacetate) Acetate), 2,4-dioxypentane titanium bis (ethyl acetoacetate), 2,4-dimethyl-2,4-dioxypentane titanium bis (ethyl acetoacetate), titanium tetrakis (ethyl acetoacetate), titanium bis ( And trimethylsiloxy) bis (ethylacetoacetate), titanium bis (trimethylsiloxy) bis (acetylacetonate), and the like. Among these, titanium diethoxide bis (ethyl acetoacetate), titanium diisopropoxide bis (ethyl acetoacetate), titanium dibutoxide bis (ethyl acetoacetate) and the like, titanium diisopropoxide bis (ethyl acetoacetate) ) Is more preferable.

  Examples of the chelating reagent capable of forming the chelate ligand of the titanium chelate include, for example, methyl acetoacetate, ethyl acetoacetate, t-butyl acetoacetate, allyl acetoacetate, acetoacetate (2-methacryloxyethyl), 3-oxo Β-ketoesters such as methyl -4,4-dimethylhexanoate and ethyl 3-oxo-4,4,4-trifluorobutanoate are mentioned, methyl acetoacetate and ethyl acetoacetate are preferred, and ethyl acetoacetate is more preferred . When two or more chelate ligands are present, each chelate ligand may be the same or different.

  The blending ratio of the (C) titanium catalyst is such that 0.1 to 40 parts by weight of the (C) titanium catalyst is blended with respect to 100 parts by weight of the (A) organic polymer, and 1 to 30 parts by weight. It is preferable to mix | blend and it is more preferable to mix | blend 1-20 mass parts. The (C) titanium catalyst may be used alone or in combination of two or more. As a method of adding the (C) titanium catalyst, in addition to directly adding the titanium chelate described above, a titanium compound capable of reacting with a chelating reagent such as titanium tetraisopropoxide or titanium diisopropoxide, and acetoacetic acid A method may be used in which a chelating reagent such as ethyl is added to the composition of the present invention and chelated in the composition.

  The curable composition of the present invention uses the titanium catalyst (C) as a curing catalyst, but other curing catalysts can be used in combination so as not to reduce the effects of the present invention. Examples of other curing catalysts include organometallic compounds and amines, and it is particularly preferable to use a silanol condensation catalyst. Examples of the silanol condensation catalyst include stannous octoate, dibutyltin dioctoate, dibutyltin dilaurate, dibutyltin maleate, dibutyltin diacetate, dibutyltin diacetylacetonate, dibutyltin oxide, dibutyltin bistriethoxysilicate, dibutyltin distearate. , Organic tin compounds such as dioctyltin dilaurate, dioctyltin diversate, tin octylate and tin naphthenate; dialkyltin oxides such as dimethyltin oxide, dibutyltin oxide and dioctyltin oxide; ; Titanates such as tetrabutyl titanate and tetrapropyl titanate; aluminum trisacetylacetonate, aluminum trisethylate Organoaluminum compounds such as acetoacetate and diisopropoxy aluminum ethyl acetoacetate; Chelate compounds such as zirconium tetraacetylacetonate and titanium tetraacetylacetonate; Lead organic acids such as lead octylate and lead naphthenate; Bismuth octylate Organic acid bismuth such as bismuth neodecanoate and bismuth rosinate; other acidic catalysts and basic catalysts known as silanol condensation catalysts. However, the toxicity of the resulting curable composition may increase depending on the amount of the organotin compound added.

  The curable composition of the present invention preferably further comprises (D) a silane compound having one hydrolyzable silicon group and one primary amino group in one molecule. (D) By adding a silane compound, storage stability and tensile physical properties can be further improved.

  As the (D) silane compound, known silane compounds having one hydrolyzable silicon group and one primary amino group in one molecule can be widely used. In the hydrolyzed silicon group of the silane compound (D), as the hydrolyzable group bonded to the silicon atom, a known hydrolyzable group excluding a primary amino group can be used, but an alkoxyl group is preferable. In the component (D), in consideration of storage stability and tensile physical properties, the hydrolyzable silicon group is preferably a trialkoxysilyl group or a dialkoxysilyl group, and more preferably a trialkoxysilyl group.

  As the (D) silane compound, a compound represented by the following formula (12) is more preferably used.

In the formula (12), R ⁴¹ is a methyl group or an ethyl group, and when a plurality of R ⁴¹ are present, they may be the same or different. R ⁴² is a methyl group or an ethyl group, and when a plurality of R ⁴² are present, they may be the same or different. R ⁴³ is a hydrocarbon group having 1 to 10 carbon atoms. m is 2 or 3, and 3 is more preferable. n is 0 or 1.

  Specific examples of the (D) silane compound include phenyltrimethoxysilane, phenyltriethoxysilane, diphenyldimethoxysilane, triphenylmethoxysilane, 2-carboxyethylphenylbis (2-methoxyethoxy) silane, and N-phenyl. Alkoxysilanes containing phenyl groups such as -3-aminopropyltrimethoxysilane, N-phenylaminomethyltrimethoxysilane; 3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropyltriethoxysilane, 3-glycidyl Alkoxysilanes containing epoxy groups such as sidoxypropylmethyldimethoxysilane, 2- (3,4-epoxycyclohexyl) ethyltrimethoxysilane, 2- (3,4-epoxycyclohexyl) ethyltriethoxysilane; Cyanate propyltrimethoxysilane, 3-isocyanatopropyltriethoxysilane, 3-isocyanatopropylmethyldiethoxysilane, 3-isocyanatopropylmethyldimethoxysilane, (isocyanatemethyl) trimethoxysilane, (isocyanatemethyl) dimethoxymethylsilane, (isocyanatemethyl) ) Alkoxysilanes containing isocyanate groups such as triethoxysilane, (isocyanatomethyl) diethoxymethylsilane; 3-mercaptopropyltrimethoxysilane, 3-mercaptopropyltriethoxysilane, 3-mercaptopropylmethyldimethoxysilane, 3-mercapto Propylmethyldiethoxysilane, mercaptomethyltriethoxysilane, mercaptomethyltrimethoxysilane, Alkoxysilanes containing mercapto groups such as captomethyltriethoxysilane; carboxysilanes such as 2-carboxyethyltriethoxysilane and N-2- (carboxymethyl) aminoethyl-3-aminopropyltrimethoxysilane; vinyltrimethoxysilane Alkoxysilanes containing vinyl unsaturated groups such as vinyltriethoxysilane, 3-methacryloyloxypropylmethyldimethoxysilane, 3-acryloyloxypropyltriethoxysilane, methacryloyloxymethyltrimethoxysilane; 3-chloropropyltrimethoxysilane Alkoxy-containing silanes such as tris (3-trimethoxysilylpropyl) isocyanurate; N-benzyl-3-aminopropyltrimethoxy Sisilane, N-vinylbenzyl-3-aminopropyltriethoxysilane, N-cyclohexylaminomethyltriethoxysilane, N-cyclohexylaminomethyldiethoxymethylsilane, N, N′-bis [3- (trimethoxysilyl) propyl] Alkoxysilanes containing secondary amino groups and / or tertiary amino groups such as ethylenediamine, bis (3-trimethoxysilylpropyl) amine, N-ethyl-3-aminoisobutyltrimethoxysilane; N- (1,3- Ketimine type silane such as dimethylbutylidene) -3- (triethoxysilyl) -1-propanamine, N- (1,3-dimethylbutylidene) -3- (trimethoxysilyl) -1-propanamine; tetramethoxy Silane, tetraethoxysilane, ethoxytrimethoxysilane, di Tetraalkoxysilanes such as toxidiethoxysilane, methoxytriethoxysilane, tetra-n-propoxysilane, tetra-i-propoxysilane, tetra-n-butoxysilane, tetra-i-butoxysilane, tetra-t-butoxysilane ( Tetraalkyl silicate); methyltrimethoxysilane, methyltriethoxysilane, methyltriisopropoxysilane, methyltriphenoxysilane, ethyltrimethoxysilane, butyltrimethoxysilane, hexyltrimethoxysilane, decyltrimethoxysilane, trifluoropropyltri Trialkoxysilanes such as methoxysilane; dialkoxysilanes such as dimethyldimethoxysilane and diethyldimethoxysilane; trimethylmethoxysilane and trimethylethoxysilane And the like can be given; the monoalkoxysilane; dimethyl isopropenoxysilane silane, alkyl isopropenoxysilane silane such as methyltrimethoxysilane isopropenoxysilane silane.

  Examples of the compound represented by the formula (12) include dialkoxysilanes such as dimethyldimethoxysilane and dimethyldiethoxysilane; methyltrimethoxysilane, methyltriethoxysilane, ethyltrimethoxysilane, ethyltriethoxysilane, and hexyltrimethoxysilane. Alkyltrialkoxysilanes such as decyltrimethoxysilane; alkoxysilanes containing phenyl groups such as phenyltrimethoxysilane and phenyltriethoxysilane; vinyl-type unsaturated groups such as vinyltrimethoxysilane and vinyltriethoxysilane Alkoxysilanes; alkoxysilanes containing epoxy groups such as 3-glycidoxypropyltrimethoxysilane and 3-glycidoxypropyltriethoxysilane; Silane is more preferable.

  The blending ratio of the (D) silane compound is not particularly limited, but it is preferable to blend 0.1 to 20 parts by mass of the (D) silane compound with respect to 100 parts by mass of the (A) organic polymer. It is more preferable to mix 0.3 to 20 parts by mass, and it is more preferable to mix 0.5 to 10 parts by mass. The (D) silane compound may be used alone or in combination of two or more.

The curable composition of the present invention preferably further contains (E) a filler. (E) A hardened | cured material can be reinforced by mix | blending a filler.
As the (E) filler, known fillers can be widely used and are not particularly limited. For example, calcium carbonate, magnesium carbonate, diatomaceous earth hydrous silicic acid, hydrous silicic acid, anhydrous silicic acid, calcium silicate , Fine powder silica, titanium dioxide, clay, talc, carbon black, slate powder, mica, kaolin, zeolite, polymer powder, etc., calcium carbonate, fine powder silica and polymer powder are preferred, surface treated carbonic acid One or more selected from the group consisting of calcium, amorphous silica having a particle size of 0.01 to 300 μm, and polymer powder having a particle size of 0.01 to 300 μm is more preferable. In addition, glass beads, silica beads, alumina beads, carbon beads, styrene beads, phenol beads, acrylic beads, porous silica, shirasu balloons, glass balloons, silica balloons, saran balloons, acrylic balloons, etc. can be used. Among them, an acrylic balloon is more preferable from the viewpoint that the decrease in elongation after curing of the composition is small.

As the calcium carbonate, any of heavy calcium carbonate, light calcium carbonate, colloidal calcium carbonate, ground calcium carbonate and the like can be used, but colloidal calcium carbonate is more preferable. These calcium carbonates may be used alone or in combination of two or more.
The primary particle diameter of the calcium carbonate is preferably 0.5 μm or less, and more preferably 0.01 to 0.1 μm. By using such fine powdered calcium carbonate having a small particle diameter, thixotropy can be imparted to the curable composition.

  Further, among calcium carbonates, surface-treated calcium carbonate is preferable, and surface-treated fine calcium carbonate is more preferable from the viewpoint of imparting thixotropy and reinforcing effect on a cured product (cured film). Furthermore, surface-treated fine powdered calcium carbonate is used in combination with other calcium carbonates such as heavy calcium carbonate that has not been surface-treated and has a large particle size, or surface-treated calcium carbonate with a large particle size. May be. When the surface-treated fine calcium carbonate and other calcium carbonate are used in combination, the ratio (mass ratio) between the surface-treated fine calcium carbonate and the other calcium carbonate is preferably 1: 9 to 9: 1, and 3: 7. ~ 7: 3 is more preferred.

  In the said surface treatment calcium carbonate, there is no restriction | limiting in particular in the surface treatment agent used, A well-known surface treatment agent can be used widely. Examples of the surface treatment agent include higher fatty acid compounds, resin acid compounds, aromatic carboxylic acid esters, anionic surfactants, cationic surfactants, nonionic surfactants, paraffin, and titanate couplings. And higher fatty acid compounds and paraffin are more preferable. These surface treatment agents may be used alone or in combination of two or more.

Examples of the higher fatty acid compounds include higher fatty acid alkali metal salts having 10 or more carbon atoms such as sodium stearate.
Examples of the resin acid-based compound include abietic acid, neoabietic acid, d-pimalic acid, i-d-pimalic acid, bodocarpic acid, benzoic acid, and cinnamic acid.
Examples of the aromatic carboxylic acid ester include phthalic acid octyl alcohol, butyl alcohol, isobutyl alcohol and the like, naphthic acid lower alcohol ester, rosin acid lower alcohol ester, and aromatic dicarboxylic acid or rosin acid malee. Examples thereof include partially esterified products of aromatic polycarboxylic acids such as acid adducts, and different alcohol esterified products.
Examples of the anionic surfactant include a sulfate ester type such as sodium dodecyl sulfate, or a sulfonic acid type anionic surfactant such as sodium dodecylbenzene sulfonate, sodium lauryl sulfonate, and dodecyl benzene sulfonic acid. Is mentioned.

  As the surface-treated calcium carbonate, known surface-treated calcium carbonate can be widely used, and is not particularly limited. For example, Vigot 15 (manufactured by Shiraishi Calcium Co., Ltd., light carbonate surface-treated with a fatty acid) Surface treated light calcium carbonate such as calcium, primary particle diameter 0.15 μm; Vigot 10 (manufactured by Shiraishi Calcium Co., Ltd., colloidal calcium carbonate surface treated with fatty acid, primary particle diameter 0.10 μm), white sinter flower DD (Shiraishi calcium Colloidal calcium carbonate surface-treated with resin acid, primary particle size 0.05 μm, Carlex 300 (manufactured by Maruo Calcium Co., Ltd., colloidal calcium carbonate surface-treated with fatty acid, primary particle size 0. 05μm), Neolite SS (manufactured by Takehara Chemical Industry Co., Ltd., surface-treated with fatty acid) Dal calcium carbonate, average particle size 0.04 μm), Neolite GP-20 (manufactured by Takehara Chemical Industry Co., Ltd., colloidal calcium carbonate surface-treated with resin acid, average particle size 0.03 μm), Calsees P (Kamishima Chemical Industry) Surface-treated colloidal calcium carbonate such as colloidal calcium carbonate surface-treated with fatty acid manufactured by Co., Ltd .; MC Coat P1 (manufactured by Maruo Calcium Co., Ltd., heavy carbonate surface-treated with paraffin) Calcium, primary particle size 3.3 μm), AFF-95 (manufactured by Pfematech Co., Ltd., heavy calcium carbonate surfaced with a cationic polymer, primary particle size 0.9 μm), AFF-Z (manufactured by Pmatech) , Heavy calcium carbonate surfaced with a cationic polymer and an antistatic agent, and a surface-treated heavy coal such as a primary particle size of 1.0 μm) Calcium and the like.

  The surface-treated calcium carbonate is preferably blended in an amount of 0 to 500 parts by weight, more preferably 10 to 300 parts by weight, and more preferably 15 to 100 parts by weight with respect to 100 parts by weight of the (A) organic polymer. More preferably. The said surface treatment calcium carbonate may be used by 1 type, and may be used in combination of 2 or more type. Moreover, you may use together the surface treatment calcium carbonate and the calcium carbonate which has not surface-treated.

As the amorphous silica, known amorphous silica can be widely used, and there is no particular limitation, but the particle size is preferably 0.01 to 300 μm, more preferably 0.1 to 100 μm. 1 to 30 μm is more preferable.
By using amorphous silica in which the difference between the refractive index of the organic polymer (A) and the refractive index of the amorphous silica is 0.1 or less, the transparency can be further improved. The difference between the refractive index of the organic polymer (A) and the refractive index of the amorphous silica is preferably 0.1 or less, more preferably 0.05 or less, and even more preferably 0.03 or less.

  The amorphous silica is preferably blended in an amount of 0 to 500 parts by weight, more preferably 1 to 200 parts by weight, and more preferably 5 to 50 parts by weight with respect to 100 parts by weight of the (A) organic polymer. More preferably. The amorphous silica may be used alone or in combination of two or more. In addition to amorphous silica having a particle diameter of 0.01 to 300 μm, amorphous silica or crystalline silica having a particle diameter range different from the above may be used in combination.

  As the polymer powder, known polymer powders can be widely used and are not particularly limited, but the particle size is preferably 0.01 to 300 μm, more preferably 0.1 to 100 μm. 1 to 30 μm is more preferable.

  As the polymer powder, for example, a monomer selected from the group consisting of (meth) acrylic acid ester, vinyl acetate, ethylene and vinyl chloride is polymerized alone, or the monomer and one or more vinyl monomers are used. A polymer powder made from a polymer obtained by copolymerization of a polymer is preferably used, an acrylic polymer powder or a vinyl polymer powder is more preferred, and an acrylic polymer powder is further preferable.

In order to further improve the transparency of the curable composition of the present invention, the difference between the refractive index of the liquid phase component containing (A) the organic polymer as the main component and the refractive index of the polymer powder is 0.1. Preferably, it is preferably 0.05 or less, more preferably 0.03 or less.
The method for setting the difference between the refractive index of the liquid phase component containing (A) the organic polymer as the main component and the refractive index of the polymer powder to 0.1 or less is not particularly limited, but (1) high (A) a method of matching the refractive index of the liquid phase component containing an organic polymer as a main component with the refractive index of the molecular powder, and (2) (A) the refractive index of the polymer powder with the refractive index of the organic polymer. And the like.

  As the method of (1), for example, (A) a method of adjusting a refractive index of a liquid phase component by blending a necessary amount of a compatible refractive index adjusting agent with a liquid phase component mainly composed of an organic polymer. Is mentioned. Specifically, (A) the refractive index of the organic polymer is about 1.46 to 1.48, and in a mode in which the refractive index of the polymer powder is higher, it is higher than (A) the organic polymer. Refractive index adjusting agent having a refractive index {for example, epoxy resin [Example: Epicoat 828 (Bisphenol A, manufactured by Yuka Shell Epoxy Co., Ltd., refractive index 1.57)], petroleum resin [Example: FTR6100 (of C5 and C9 Copolymer, Mitsui Petrochemical Co., Ltd., refractive index 1.56)], terpene phenol resin [Example: Polystar T145 (Yasuhara Chemical Co., Ltd., refractive index 1.59)]} There is a method of heating and melting the coalescence.

  Examples of the method (2) include a method of appropriately changing the monomer composition of the polymer powder. Specifically, (A) the refractive index of the polymer powder is an aspect in which the refractive index of the organic polymer is about 1.46 to 1.48 and acrylic polymer powder is used as the polymer powder. As a method for increasing the viscosity, for example, a monomer such as vinyl chloride [refractive index 1.53 (polymer)] and allylonitrile [refractive index 1.52 (polymer)] is used as a single monomer of (meth) acrylate. And a method of copolymerizing with a body. In this embodiment, the method (E4) for reducing the refractive index of the polymer powder includes, for example, lauryl methacrylate [refractive index 1.44 (monomer)], allyl methacrylate [refractive index 1.44 (single Monomer)], 2 (2-ethoxyethoxy) ethyl acrylate [refractive index 1.43 (monomer)] and the like are copolymerized with a meth) acrylate monomer.

  The polymer powder is preferably blended in an amount of 0 to 500 parts by weight, more preferably 0.5 to 100 parts by weight, based on 100 parts by weight of the organic polymer (A), and 1 to 50 parts by weight. It is more preferable to blend. The polymer powder may be used alone or in combination of two or more.

  In the curable composition of the present invention, the blending ratio of the (E) filler is not particularly limited. It is preferable to mix 2 parts by weight, more preferably 2 to 250 parts by weight, and even more preferably 5 to 125 parts by weight. The (E) filler may be used alone or in combination of two or more.

The curable composition of the present invention preferably further contains (F) a diluent. (F) Physical properties, such as a viscosity, can be adjusted by mix | blending a diluent.
(F) As a diluent, a well-known diluent can be widely used and there is no restriction | limiting in particular, For example, saturated hydrocarbon type solvents, such as normal paraffin and isoparaffin, a linearlen dimer (Idemitsu Kosan Co., Ltd. brand name) Α-olefin derivatives represented by the following formula (I) such as, aromatic hydrocarbon solvents such as toluene and xylene, alcohols such as ethanol, propanol, butanol, pentanol, hexanol, octanol, decanol, diacetone alcohol, etc. Various solvents such as solvents, ester solvents such as ethyl acetate, butyl acetate, amyl acetate and cellosolve, citric acid ester solvents such as acetyltriethyl citrate, and ketone solvents such as methyl ethyl ketone and methyl isobutyl ketone can be used.
R ⁵¹ -ZR ⁵² (I)
(In the formula (I), R ⁵¹ and R ⁵² each independently represents a linear alkyl group having 2 to 20 carbon atoms, and Z is represented by any one of the following formulas (Ia) to (Ic). Represents a valent group.)

(In the formula (Ib), R ⁵³ represents a hydrogen atom or a linear or branched alkyl group having 1 to 40 carbon atoms.)

The flash point of the diluent (F) is not particularly limited, but in view of the safety of the resulting curable composition, it is desirable that the curable composition has a high flash point. Volatile substances from the curable composition Is preferably less.
Therefore, the flash point of the (F) diluent is preferably 60 ° C. or higher, and more preferably 70 ° C. or higher. When two or more (F) diluents are mixed and used, the flash point of the mixed diluent is preferably 70 ° C. or higher. However, generally, a diluent having a high flash point tends to have a low dilution effect on the curable composition, and therefore, the flash point is preferably 250 ° C. or lower.

  In consideration of both safety and dilution effect of the curable composition of the present invention, as the diluent (F), a saturated hydrocarbon solvent is preferable, and normal paraffin and isoparaffin are more preferable. The normal paraffin and isoparaffin preferably have 10 to 16 carbon atoms. Specifically, N-11 (normal paraffin, manufactured by JX Nippon Oil & Energy Corporation, carbon number 11, flash point 68 ° C), N-12 (normal paraffin, manufactured by JX Nippon Oil & Energy Corporation, carbon number) 12, flash point 85 ° C.), IP solvent 2028 (isoparaffin, manufactured by Idemitsu Kosan Co., Ltd., carbon number 10 to 16, flash point 86 ° C.) and the like.

  The blending ratio of the (F) diluent is not particularly limited, but 0 to 50 parts by weight of the (F) diluent is preferably blended with respect to 100 parts by weight of the (A) organic polymer. It is more preferable to mix 1 to 30 parts by mass, and further preferable to mix 0.1 to 15 parts by mass. The said (F) diluent may be used by 1 type, and may be used in combination of 2 or more type.

The curable composition of the present invention preferably further contains a metal hydroxide. By mix | blending the said metal hydroxide, a flame retardance can be provided, workability | operativity can be improved, and hardened | cured material can be reinforced. Furthermore, the metal hydroxide also has an effect of higher safety than other flame retardants such as halogen flame retardants. In particular, by using a metal hydroxide and surface-treated calcium carbonate in combination, workability (thixotropic properties) can be further improved and flame retardancy can be imparted. The metal hydroxide may be a metal hydroxide surface-treated with a surface treatment agent.
Examples of the metal hydroxide include aluminum hydroxide and magnesium hydroxide, and aluminum hydroxide is more preferable.

  The blending ratio of the metal hydroxide is not particularly limited, but it is preferable to blend 0 to 500 parts by weight of the metal hydroxide with respect to 100 parts by weight of the (A) organic polymer, and 2 to 250 parts by weight. More preferably, it is more preferably 5 to 125 parts by mass. The said metal hydroxide may be used independently and may be used together 2 or more types. Moreover, you may use together another well-known flame retardant.

  In addition to the above-described components, the curable composition of the present invention includes an ultraviolet absorber, an antioxidant, an anti-aging agent, an adhesiveness imparting agent, a physical property modifier, a plasticizer, a thixotropic agent, and a dehydration agent as necessary. You may mix substances such as additives (storage stability improvers), flame retardants, tackifiers, anti-sagging agents, colorants, radical polymerization initiators, and blend with other compatible polymers. Good.

  The antioxidant is used to prevent oxidation of the curable composition to improve weather resistance and heat resistance, and examples thereof include hindered amine-based and hindered phenol-based antioxidants. It is done. Examples of the hindered amine antioxidant include N, N ′, N ″, N ″ ′-tetrakis- (4,6-bis (butyl- (N-methyl-2,2,6,6-tetramethylpiperidine- 4-yl) amino) -triazin-2-yl) -4,7-diazadecane-1,10-diamine, dibutylamine 1,3,5-triazine N, N'-bis- (2,2,6 , 6-tetramethyl-4-piperidyl-1,6-hexamethylenediamine · N- (2,2,6,6-tetramethyl-4-piperidyl) butylamine polycondensate, poly [{6- (1, 1,3,3-tetramethylbutyl) amino-1,3,5-triazine-2,4-diyl} {(2,2,6,6-tetramethyl-4-piperidyl) imino} hexamethylene {(2 , 2,6,6-tetramethyl-4- Peridyl) imino}], a polymer of dimethyl succinate and 4-hydroxy-2,2,6,6-tetramethyl-1-piperidineethanol, [bis (2,2,6,6-tetramethyl-decanedioic acid) 1 (octyloxy) -4-piperidyl) ester, reaction product of 1,1-dimethylethyl hydroperoxide and octane (70%)]-polypropylene (30%), bis (1,2,2,6,6- Pentamethyl-4-piperidyl) [[3,5-bis (1,1-dimethylethyl) -4-hydroxyphenyl] methyl] butyl malonate, methyl 1,2,2,6,6-pentamethyl-4-piperidyl seba Kate, bis (2,2,6,6-tetramethyl-4-piperidyl) sebacate, bis (1,2,2,6,6-pentamethyl-4-piperidyl) sebacate 1- [2- [3- (3,5-Di-tert-butyl-4-hydroxyphenyl) propionyloxy] ethyl] -4- [3- (3,5-di-tert-butyl-4-hydroxyphenyl) ) Propionyloxy] -2,2,6,6-tetramethylpiperidine, 4-benzoyloxy-2,2,6,6-tetramethylpiperidine, 8-acetyl-3-dodecyl-7,7,9,9- Examples include, but are not limited to, tetramethyl-1,3,8-triazaspiro [4.5] decane-2,4-dione, etc. Examples of hindered phenol antioxidants include pentane. Erythritol-tetrakis [3- (3,5-di-tert-butyl-4-hydroxyphenyl) propionate], thiodiethylene-bis [3- (3,5-di-ter t-butyl-4-hydroxyphenyl) propionate], octadecyl-3- (3,5-di-tert-butyl-4-hydroxyphenyl) propionate], N, N′-hexane-1,6-diylbis [3- (3,5-di-tert-butyl-4-hydroxyphenylpropioamide), benzenepropanoic acid 3,5-bis (1,1-dimethylethyl) -4-hydroxy C7-C9 side chain alkyl ester, 2,4 -Dimethyl-6- (1-methylpentadecyl) phenol, diethyl [[3,5-bis (1,1-dimethylethyl) -4-hydroxyphenyl] methyl] phosphonate, 3,3 ', 3 ", 5 5 ', 5 "-hexane-tert-butyl-4-a, a', a"-(mesitylene-2,4,6-tolyl) tri-p-cresol, calci Mudiethylbis [[[3,5-bis- (1,1-dimethylethyl) -4-hydroxyphenyl] methyl] phosphonate], 4,6-bis (octylthiomethyl) -o-cresol, ethylenebis (oxyethylene) Bis [3- (5-tert-butyl-4-hydroxy-m-tolyl) propionate], hexamethylenebis [3- (3,5-di-tert-butyl-4-hydroxyphenyl) propionate], 1,3 , 5-Tris (3,5-di-tert-butyl-4-hydroxybenzyl) -1,3,5-triazine-2,4,6- (1H, 3H, 5H) -trione, N-phenylbenzenamine Product of 2,4,4-trimethylpentene with 2,6-di-tert-butyl-4- (4,6-bis (octylthio) -1,3,5 Triazin-2-ylamino) phenol and the like, but not limited thereto. The antioxidants may be used alone or in combination of two or more.

  The ultraviolet absorber is used to improve the weather resistance by preventing photodegradation of the curable composition, for example, ultraviolet absorption of benzotriazole, triazine, benzophenone, benzoate, etc. Agents and the like. Examples of the ultraviolet absorber include 2,4-di-tert-butyl-6- (5-chlorobenzotriazol-2-yl) phenol and 2- (2H-benzotriazol-2-yl) -4,6- Di-tert-pentylphenol, 2- (2H-benzotriazol-2-yl) -4- (1,1,3,3-tetramethylbutyl) phenol, methyl 3- (3- (2H-benzotriazole-2) -Yl) -5-tert-butyl-4-hydroxyphenyl) propionate / polyethylene glycol 300 reaction product, 2- (2H-benzotriazol-2-yl) -6- (linear and side chain dodecyl) -4 -Benzotriazole ultraviolet absorbers such as methylphenol, 2- (4,6-diphenyl-1,3,5-triazin-2-yl) -5-[(he Sil) oxy] -phenol and the like triazine ultraviolet absorbers, benzophenone ultraviolet absorbers such as octabenzone, 2,4-di-tert-butylphenyl-3,5-di-tert-butyl-4-hydroxybenzoate, etc. Examples include, but are not limited to, benzoate ultraviolet absorbers. The said ultraviolet absorber may be used independently or may use 2 or more types together.

  The anti-aging agent is used to prevent heat deterioration of the curable composition and improve heat resistance. For example, an anti-aging agent such as an amine-ketone type and an aromatic secondary amine type are used. Antiaging agents, benzimidazole type antiaging agents, thiourea type antiaging agents, phosphorous acid type antiaging agents and the like can be mentioned.

  Examples of the amine-ketone-based anti-aging agent include 2,2,4-trimethyl-1,2-dihydroquinoline polymer, 6-ethoxy-1,2-dihydro-2,2,4-trimethylquinoline. And amine-ketones such as a reaction product of diphenylamine and acetone, but are not limited thereto.

  Examples of the aromatic secondary amine antioxidant include N-phenyl-1-naphthylamine, alkylated diphenylamine, octylated diphenylamine, 4,4′-bis (α, α-dimethylbenzyl) diphenylamine, p- (P-toluenesulfonylamide) diphenylamine, N, N′-di-2-naphthyl-p-phenylenediamine, N, N′-diphenyl-p-phenylenediamine, N-phenyl-N′-isopropyl-p-phenylenediamine N-phenyl-N ′-(1,3-dimethylbutyl) -p-phenylenediamine, N-phenyl-N ′-(3-methacryloyloxy-2-hydroxypropyl) -p-phenylenediamine, etc. Secondary amines and the like can be mentioned, but the invention is not limited to these.

  Examples of the benzimidazole antioxidant include benzimidazoles such as 2-mercaptobenzimidazole, 2-mercaptomethylbenzimidazole, and zinc salt of 2-mercaptobenzimidazole, but are not limited thereto. is not.

  Examples of the thiourea antioxidant include, but are not limited to, thiourea such as 1,3-bis (dimethylaminopropyl) -2-thiourea and tributylthiourea.

  Examples of the phosphite antioxidant include, but are not limited to, phosphites such as tris (nonylphenyl) phosphite.

  Although the usage-amount of an anti-aging agent does not have a restriction | limiting in particular, Preferably it is 0.1-20 mass parts with respect to 100 mass parts of said (A) organic polymers, More preferably, 0.2-10 mass parts. More preferably, it is suitable to use in the range of 0.2 to 5 parts by mass.

  The physical property modifier is added for the purpose of improving physical properties of the curable composition such as tensile physical properties. As an example of the physical property adjusting agent, for example, a silicon compound having one silanol group and one primary amino group in one molecule is preferably used. Examples of the silicon compound include triphenylsilanol, trialkylsilanol, dialkylphenylsilanol, diphenylalkylsilanol and the like.

  The plasticizer is added for the purpose of enhancing the elongation physical properties after curing or enabling low modulus. The type of the plasticizer is not particularly limited. For example, phthalic acid esters such as dioctyl phthalate, dibutyl phthalate, butyl benzyl phthalate, diisodecyl phthalate, diisoundecyl phthalate; dioctyl adipate, isodecyl succinate, sebacine Aliphatic dibasic acid esters such as dioctyl acid and dibutyl adipate; Glycol esters such as diethylene glycol dibenzoate, dipropylene glycol dibenzoate and pentaerythritol ester; Aliphatics such as butyl oleate and methyl acetylricinoleate Esters; Phosphate esters such as tricresyl phosphate, trioctyl phosphate, octyl diphenyl phosphate, tributyl phosphate, tricresyl phosphate; Epoxy plasticizers such as modified soybean oil, epoxidized linseed oil, and epoxy benzyl stearate; Polyester plasticizers such as polyesters of dibasic acids and dihydric alcohols; Polyethers such as polypropylene glycol and polyethylene glycol derivatives Diethylene glycol dimethyl ether, diethylene glycol ethyl methyl ether, diethylene glycol diethyl ether, etc. with 2 repetitions, triethylene glycol diethyl ether, triethylene glycol ethyl methyl ether, triethylene glycol diethyl ether, etc. with 3 repetitions, tetraethylene glycol 4 repeats such as diethyl ether, tetraethylene glycol ethyl methyl ether, tetraethylene glycol diethyl ether, etc. , Polyoxyethylene alkyl ethers such as polyoxyethylene dimethyl ether having a higher repetition; polystyrenes such as poly-α-methylstyrene and polystyrene; polybutadiene, butadiene-acrylonitrile copolymer, polychloroprene, polyisoprene, polybutene, water Hydrocarbon oligomers such as hydrogenated polybutadiene, hydrogenated polyisoprene and process oil; chlorinated paraffins; acrylics such as UP-1080 (manufactured by Toagosei Co., Ltd.) and UP-1061 (manufactured by Toagosei Co., Ltd.) Hydroxyl group-containing acrylic plasticizers such as UP-2000 (manufactured by Toagosei Co., Ltd.), UHE-2012 (manufactured by Toagosei Co., Ltd.); UC-3510 (manufactured by Toagosei Co., Ltd.) Carboxyl group-containing acrylic polymers such as UG-4; Epoxy group-containing acrylic polymers such as 00 (manufactured by Toagosei Co., Ltd.); less than 0.8 such as US-6110 (manufactured by Toagosei Co., Ltd.), US-6120 (manufactured by Toagosei Co., Ltd.) , Preferably less than 0.4 silyl group-containing acrylic polymers; oxyalkylene resins containing less than 0.8, preferably less than 0.4 silyl groups are exemplified.

  Examples of the thixotropic agent include inorganic thixotropic agents such as colloidal silica and asbestos powder, organic thixotropic agents such as organic bentonite, modified polyester polyol, and fatty acid amide, hydrogenated castor oil derivative, fatty acid amide wax, and aluminum stearylate. And barium stearylate.

  The dehydrating agent is added for the purpose of removing moisture during storage. Examples of the dehydrating agent include zeolite, calcium oxide, magnesium oxide, and zinc oxide.

  Examples of the flame retardant include phosphorus flame retardants such as red phosphorus and ammonium polyphosphate; metal oxide flame retardants such as antimony trioxide; bromine flame retardants; chlorine flame retardants and the like.

  The curable composition of the present invention can be a one-component type or a two-component type as required, but can be suitably used particularly as a one-component type. The curable composition of the present invention can be cured at normal temperature by moisture in the atmosphere, and is suitably used as a normal temperature moisture-curable curable composition, but if necessary, curing is accelerated by heating as appropriate. You may let them.

  The method for producing the curable composition of the present invention is not particularly limited. For example, a predetermined amount of the components (A) to (C) is blended, and other blending substances are blended as necessary, followed by deaeration and stirring. Can be manufactured. In addition, the reaction between the epoxysilane compound and the aminosilane compound in the (B) silane compound is carried out using the (B) silane compound obtained by reacting the epoxysilane compound and the aminosilane compound in advance. And other compounding materials may be blended to prepare a curable composition, or a mixture in which some or all of the epoxysilane compound, aminosilane compound, and other compounding materials are mixed is prepared in the mixture. The curable composition may be prepared by reacting an epoxysilane compound and an aminosilane compound.

  The blending order of the components (A) to (C) is not particularly limited, but the components (B) and (C) are mixed in advance to obtain a mixture containing the components (B) and (C), and then the mixture. And a component (A) are preferably blended, and a curing catalyst obtained by aging a mixture containing the components (B) and (C) at a predetermined temperature is more preferably blended with the component (A). Here, aging means transesterification of a part of the alkoxy group of the (C) titanium catalyst and a part of the alkoxy group of the (B) silane compound and / or the moisture contained in the air ( B) This means that a part of the silane compound is hydrolyzed with the titanium catalyst (C) and oligomerized. It is preferable to reach the state of chemical equilibrium by the aging.

  When a mixture in which the (B) silane compound and the (C) titanium catalyst are mixed in advance is used, the mixing ratio of the (B) silane compound and the (C) titanium catalyst is 1 mol of the (C) titanium catalyst. On the other hand, the range of 0.1-30 mol of said (B) silane compound is preferable, the range of 0.5-5.0 mol is more preferable, The range of 0.5-3.0 mol is further more preferable. The (C) titanium catalyst and the (B) silane compound may be used singly or in combination of two or more.

  The method of obtaining the mixture of the (B) silane compound and the (C) titanium catalyst is obtained by using the (B) silane compound obtained by reacting an epoxy silane compound and an aminosilane compound in advance. The compound and (C) titanium catalyst may be mixed to obtain a mixture, or an epoxy silane compound, an amino silane compound, and (C) a mixture of titanium catalyst are prepared, and the epoxy silane compound and amino silane compound in the mixture And (B) a mixture of a silane compound and (C) a titanium catalyst may be obtained.

  The reaction temperature condition for aging the mixture containing the (B) silane compound and the (C) titanium catalyst is not particularly limited, but the (B) silane compound and the (C) titanium catalyst are heated at 30 ° C to 100 ° C. It is preferable to make it react, 30 to 90 degreeC is more preferable, and 40 to 80 degreeC is further more preferable. By setting the reaction temperature within the above range, the reaction can proceed stably without causing runaway. When the reaction temperature is less than 30 ° C., the activity is low, the time required to achieve a sufficient reaction is lengthened, and the efficiency is poor. The reaction time can be appropriately set in consideration of the reaction temperature and the like, but it is desirable to carry out the reaction until at least an equilibrium state is reached. For example, the reaction time is usually 1 to 336 hours under the above conditions, preferably Is preferably set within a range of 72 to 168 hours.

  The blending order of other blending substances other than components (A) to (C) is not particularly limited, and may be determined as appropriate. When using a mixture in which the components (B) and (C) are mixed in advance, the mixture may be obtained by mixing other compounding substances together with the components (B) and (C). The components (B) and (C) After blending one of the above and the other blending substance, the other of components (B) and (C) may be blended to obtain a mixture, and other blends may be added to the mixture containing components (B) and (C). Substances may be added. In the case of using a curing catalyst obtained by aging a mixture containing components (B) and (C), other compounding substances are added before the aging step, and the mixture contains components (B), (C) and other compounding substances. A ripening step may be performed, or other compounding substances may be added after the aging process, or other compounding substances may be added after the aging process and further ripened at a predetermined temperature. Moreover, you may age | cure | ripen at the predetermined temperature further with respect to the composition which mix | blended all the compounding substances.

  When the component (D) is blended as another blending substance, there is no particular limitation in the blending order, but after obtaining a mixture in which the components (C) and (D) are mixed in advance, the mixture and the components (A) and ( After obtaining the mixture which mix | blended B) or mixed component (B)-(D) previously, this mixture and component (A) are mix | blended, etc., and the mixture containing component (C) and (D) is obtained. After that, it is preferable to blend the remaining compounding substances.

  When a mixture in which the (C) titanium catalyst and the (D) silane compound are mixed in advance is used, the mixing ratio of the (C) titanium catalyst and the (D) silane compound is 1 mol of the (C) titanium catalyst. On the other hand, the range of 0.1-30 mol of said (D) silane compound is preferable, the range of 0.5-5.0 mol is more preferable, The range of 0.5-3.0 mol is further more preferable. The (C) titanium catalyst and the (D) silane compound may be used singly or in combination of two or more.

  When a silane compound having an alkoxysilyl group is used as the component (D), a curing catalyst obtained by aging a mixture containing the components (C) and (D) at a predetermined temperature may be blended with the remaining compounding substances. preferable. Here, aging means transesterification of a part of the alkoxy group of the (C) titanium catalyst and a part of the alkoxy group of the (D) silane compound and / or moisture contained in the air ( D) It means that a part of the silane compound is hydrolyzed with the titanium catalyst (C) and oligomerized. It is preferable to reach the state of chemical equilibrium by the aging.

  The reaction temperature condition for aging the mixture containing the (C) titanium catalyst and the (D) silane compound is not particularly limited, but the (C) titanium catalyst and the (D) silane compound are heated at 30 ° C to 100 ° C. It is preferable to make it react, 30 to 90 degreeC is more preferable, and 40 to 80 degreeC is further more preferable. By setting the reaction temperature within the above range, the reaction can proceed stably without causing runaway. When the reaction temperature is less than 30 ° C., the activity is low, the time required to achieve a sufficient reaction is lengthened, and the efficiency is poor. The reaction time can be appropriately set in consideration of the reaction temperature and the like, but it is desirable to carry out the reaction until at least an equilibrium state is reached. For example, the reaction time is usually 1 to 336 hours under the above conditions, preferably Is preferably set within a range of 72 to 168 hours.

  In the present invention, the ripening of the components (B) and (C) and the ripening of the components (C) and (D) may or may not be performed, but at least one of the aging is performed. It is preferable to perform both aging. In the case of aging, there is no restriction on the order of aging, but since the manufacturing process is simplified, from the viewpoint of workability, aging is simultaneously performed at a predetermined temperature for the mixture in which components (B) to (D) are mixed In view of storage stability, rate of change in curing time, and the like, after aging a mixture containing one of components (B) and (D) and component (C) at a predetermined temperature, A method in which the other of (B) and (D) is blended and aged again at a predetermined temperature as necessary, a component (B) and a component (C) are aged, a component (B) and a component (D ) Is preferably mixed, and if necessary, the mixed mixture is further aged. By performing the aging step, the storage stability can be further improved.

  When the component (E) is blended as another blending substance, there is no particular limitation on the blending order, and it may be determined appropriately. When the components (B) and (C) are aged and the components (C) and (D) are aged, it is preferable to add the component (E) after the aging step.

  When component (F) is blended as another blending substance, there is no particular limitation on the order of blending, but in addition to one or both of components (B) and (D) and component (C), component (F) is added. It is preferable to age the mixture at a predetermined temperature. In this case, the mixture containing one or both of the components (B) and (D), the component (C), and the component (F) may be simultaneously aged at a predetermined temperature. A mixture containing one or both of D) and the component (C) is aged at a predetermined temperature at the same time, and then the component (F) is blended in the mixture and aged again at a predetermined temperature, for example, a plurality of times. An aging step may be performed. In particular, by blending the component (F) after the aging step of the components (B) to (D) and further performing the aging step, the rate of change in the curing time after storage can be reduced, which is more preferable. By performing the aging step, the storage stability can be further improved.

  The curable composition of the present invention can be used as an adhesive, a sealing material, an adhesive material, a coating material, a potting material, a paint, a putty material, a primer, and the like. Since the curable composition of the present invention is excellent in adhesiveness, storage stability, and curability, it is particularly preferable to use it as an adhesive, but for various other buildings, automobiles, civil engineering, electric / electronics. It can be used for fields.

  The present invention will be described more specifically with reference to the following examples. However, it is needless to say that these examples are shown by way of illustration and should not be construed in a limited manner.

Analysis and measurement in Synthesis Examples, Examples and Comparative Examples were performed according to the following methods.
1) Measurement of number average molecular weight It measured on the following conditions by the gel permeation chromatography (GPC). In the present invention, the maximum frequency molecular weight measured by GPC under the measurement conditions and converted with standard polyethylene glycol is referred to as the number average molecular weight.
THF solvent measuring device / analyzer: Alliance (manufactured by Waters), 2410 type differential refraction detector (manufactured by Waters), 996 type multi-wavelength detector (manufactured by Waters), Millenium data processing device (manufactured by Waters)
Column: Plgel GUARD + 5 μmMixed-C × 3 (50 × 7.5 mm, 300 × 7.5 mm: manufactured by Polymer Lab)
・ Flow rate: 1 mL / min ・ Converted polymer: Polyethylene glycol ・ Measurement temperature: 40 ° C.
FT-NMR measuring apparatus: JNM-ECA500 (500 MHz) manufactured by JEOL Ltd.
FT-IR measuring device: FT-IR460Plus manufactured by JASCO Corporation

2) Storage stability test, curability (TFT) test, and thixotropy test Viscosity, curing time, and structural viscosity index (SVI value) immediately after blending the curable composition were measured. The conditions were referred to as initial, and the measured viscosity, curing time, and SVI value were defined as initial viscosity, initial TFT, and initial SVI value, respectively.

The viscosity is measured with a BS rotational viscometer (rotor No. 7-10 rpm) when the viscosity of the curable composition is 160 Pa · s or higher, and the BH type when the viscosity of the curable composition is less than 160 Pa · s. It measured with the rotational viscometer (rotor No.7-20rpm) (measurement temperature 23 degreeC).
As for the curing time, the touch drying time (TFT) was measured in an environment of RH 50% at 23 ° C. according to JIS A 1439 5.19 tack-free test.
The SVI value is calculated by dividing the viscosity at 1 rpm by the viscosity at 10 rpm using a BS type rotational viscometer (rotor No. 7) when the viscosity of the curable composition is 160 Pa · s or more. When the viscosity of the product was less than 160 Pa · s, it was calculated by dividing the viscosity at 2 rpm by the viscosity at 20 rpm using a BH type rotational viscometer (rotor No. 7) (measurement temperature 23 ° C.). The obtained SVI value was used as an index indicating thixotropy.

Next, the curable composition in the sealed glass container was left in an atmosphere of 50 ° C. for 1, 2 or 4 weeks, and the viscosity, the curing time, and the SVI value were measured. The measured viscosity, curing time, and SVI value were the viscosity after storage, the TFT after storage, and the SVI value after storage, respectively.
The viscosity increase ratio was calculated by dividing the viscosity after storage by the initial viscosity. Moreover, the thickening rate after 1 week storage was evaluated according to the following evaluation criteria.
A: 0.90 to 1.40, O: 1.41 to 1.50, Δ: 1.51 to 1.60, x: 1.61 to 0.89.
The rate of change was calculated by dividing the TFT after storage by the initial TFT. The rate of change after storage for 1 week was evaluated according to the following evaluation criteria.
A: 0.90 to 1.10, B: 0.80 to 0.89, or 1.11 to 1.30, Δ: 1.31 to 1.40, or 0.70 to 0.79 Hereinafter, x: 1.41 or more or 0.69 or less.

3) Surface Curability Test A cured product of a curable composition having a size of 100 mm × 100 mm × 3 mm was prepared by leaving it in an environment of 23 ° C. and RH 50% for 7 days, and judged by finger touch. The evaluation criteria are as follows.
A: Not sticky at all, ○: Not sticky, △: Sticky, ×: Very sticky.

4) Adhesion test 0.2 g of the curable composition was uniformly applied on the adherend, and immediately bonded in an area of 25 mm × 25 mm. After bonding, the adhesive strength was measured according to the tensile shear adhesive strength test method of a rigid adherend immediately after pressing with a small eyeball clip for 7 days in an atmosphere of 23 ° C. and RH 50%. As an adherend, hard vinyl chloride (PVC), polycarbonate (PC), polystyrene (PS), ABS resin (ABS), acrylic resin (PMMA), nylon 6 (6-Ny), cold rolled steel plate (SPCC), Alternatively, anodized aluminum (Al) was used. Further, the fracture state of the adhesive surface was evaluated according to the following evaluation criteria.
CF: cohesive failure, AF: adhesive failure, C10A90 to C90A10: The area of the fractured state of CF and AF is expressed as an approximate percentage. CnA (100-n) is CFn%, AF (100-n)% It means the destruction state.

5) Transparency test The curable composition was stretched using a 3 mm spacer between acrylic plates having a thickness of 2 mm, and the transparency was visually observed and evaluated according to the following evaluation criteria.
◎: colorless and transparent, ○: colorless and slightly cloudy, ×: cloudy.

(Synthesis Example 1)
Hydroxyl value obtained by reacting propylene oxide in the presence of zinc hexacyanocobaltate-glyme complex catalyst with ethylene glycol as initiator in a flask equipped with a stirrer, nitrogen gas inlet tube, thermometer and reflux condenser A polyoxypropylene triol having a reduced molecular weight of 24,000 and a molecular weight distribution of 1.3 was obtained. A methanol solution of sodium methoxide is added to the obtained polyoxypropylene diol, and methanol is distilled off under reduced pressure by heating to convert the terminal hydroxyl group of the polyoxypropylene triol into sodium alkoxide to obtain a polyoxyalkylene polymer M1. It was.

Next, the polyoxyalkylene polymer M1 is reacted with allyl chloride at the blending ratio shown in Table 1 to remove unreacted allyl chloride and purified to obtain a polyoxyalkylene polymer having an allyl group at the terminal. Coalescence was obtained. This polyoxyalkylene polymer having an allyl group at the end is reacted with trimethoxysilane, which is a silicon hydride compound, by adding 150 ppm of a platinum vinylsiloxane complex isopropanol solution having a platinum content of 3 wt%, and trimethoxysilyl at the end. A polyoxyalkylene polymer A1 having a group was obtained.
As a result of measuring the molecular weight of the obtained polyoxyalkylene polymer A1 having a trimethoxysilyl group by GPC, the peak top molecular weight was 25,000 and the molecular weight distribution was 1.3. According to H ¹ -NMR measurement, the number of terminal trimethoxysilyl groups was 1.7 per molecule.

(Synthesis Example 2)
Hydroxyl value obtained by reacting propylene oxide in the presence of zinc hexacyanocobaltate-glyme complex catalyst with ethylene glycol as initiator in a flask equipped with a stirrer, nitrogen gas inlet tube, thermometer and reflux condenser A polyoxypropylene diol having a converted molecular weight of 11000 and a molecular weight distribution of 1.3 was obtained. A methanol solution of sodium methoxide is added to the obtained polyoxypropylene triol, methanol is distilled off under heating and reduced pressure, and the terminal hydroxyl group of the polyoxypropylene triol is converted to sodium alkoxide to obtain a polyoxyalkylene polymer M2. It was.

Next, the polyoxyalkylene polymer M2 is reacted with allyl chloride at the blending ratio shown in Table 1 to remove unreacted allyl chloride, and purified to obtain a polyoxyalkylene polymer having an allyl group at the terminal. Coalescence was obtained. This polyoxyalkylene polymer having an allyl group at the end is reacted with trimethoxysilane, which is a silicon hydride compound, by adding 150 ppm of a platinum vinylsiloxane complex isopropanol solution having a platinum content of 3 wt%, and trimethoxysilyl at the end. A polyoxyalkylene polymer A2 having a group was obtained.
As a result of measuring the molecular weight of the obtained polyoxyalkylene polymer A2 having a trimethoxysilyl group by GPC, the peak top molecular weight was 12,000 and the molecular weight distribution was 1.3. According to H ¹ -NMR measurement, the number of terminal trimethoxysilyl groups was 1.7 per molecule.

  In Table 1, the compounding quantity of each compounding substance is shown by g. The polyoxyalkylene polymers M1 and M2 are the polyoxyalkylene polymers M1 and M2 obtained in Synthesis Examples 1 and 2, respectively.

(Synthesis Example 3)
As shown in Table 2, 184 g of ethyl acetate (manufactured by Wako Pure Chemical Industries, Ltd.) was put into a flask equipped with a stirrer, a nitrogen gas inlet tube, a thermometer, a dropping device and a reflux condenser, and heated to 70 ° C. did. In another container, 247 g of methyl methacrylate, 23 g of n-butyl acrylate, 56 g of lauryl methacrylate (trade name: Light Ester L, manufactured by Kyoeisha), 3-acryloxypropyltrimethoxysilane (trade name: KBM5103, Shin-Etsu Chemical Co., Ltd.) 58.64g, 26.21g of 3-mercaptopropyltrimethoxysilane, and 15.73g of AIBN were mixed, stirred, filled into a dropping device, and dropped over 3 hours. After completion of dropping, the reaction was further continued for 3 hours to obtain a vinyl polymer A3 having a trimethoxysilyl group.
As a result of measuring the molecular weight of the obtained vinyl polymer A3 by GPC, the peak top molecular weight was 3000 and the molecular weight distribution was 1.6. The number of trimethoxysilyl groups contained by H ¹ -NMR measurement was 2.00 per molecule.

(Synthesis Example 4)
As shown in Table 2, in a flask equipped with a stirrer, a nitrogen gas inlet tube, a thermometer, and a reflux condenser, m-xylene 43.00 g, methyl methacrylate 80.00 g, 2-ethylhexyl methacrylate (Tokyo Chemical Industry Co., Ltd.) )) 20.00 g, acryloxymethyltrimethoxysilane (manufactured by Gelest) 20.00 g, and 0.10 g of zirconocene dichloride as a metal catalyst were charged, and the contents of the flask were brought to 80 ° C. while introducing nitrogen gas into the flask. Heated. Next, 3.65 g of mercaptomethyltrimethoxysilane sufficiently substituted with nitrogen gas was added all at once to the flask with stirring. After adding 3.65 g of mercaptomethyltrimethoxysilane, heating and cooling were performed for 4 hours so that the temperature of the contents in the stirring flask could be maintained at 80 ° C. Further, 3.65 g of mercaptomethyltrimethoxysilane sufficiently substituted with nitrogen gas was added to the flask over 5 minutes with stirring. After the addition of 3.65 g of the total amount of mercaptomethyltrimethoxysilane, the reaction was carried out for 4 hours while further cooling and heating so that the temperature of the contents in the stirring flask could be maintained at 90 ° C. After a total of 8 hours and 5 minutes of reaction, the temperature of the reaction product was returned to room temperature, 20.00 g of a benzoquinone solution (95% THF solution) was added to the reaction product to stop the polymerization, and a vinyl system having a trimethoxysilyl group A polymer A4 was obtained.
As a result of measuring the molecular weight of the obtained vinyl polymer A4 by GPC, the peak top molecular weight was 4000, and the molecular weight distribution was 1.6. The number of trimethoxysilyl groups contained by H ¹ -NMR measurement was 2.00 per molecule.

(Synthesis Example 5)
As shown in Table 2, a polyoxyalkylene polymer having a trimethoxysilyl group at the terminal obtained in Synthesis Example 1 in a flask equipped with a stirrer, a nitrogen gas inlet tube, a thermometer, a dropping device, and a reflux condenser. 400 g of A1 and 200 g of polyoxyalkylene polymer A2 having a trimethoxysilyl group at the terminal obtained in Synthesis Example 2 were added and heated to 80 ° C. In another container, 247 g of methyl methacrylate (trade name: Light Ester M, manufactured by Kyoeisha Co., Ltd.), 23 g of n-butyl acrylate, 49 g of stearyl methacrylate (trade name: Light Ester S, manufactured by Kyoeisha Co., Ltd.), 3-methacryloxy 45 g of propyltrimethoxysilane (trade name: KBM503, manufactured by Shin-Etsu Chemical Co., Ltd.), 23.77 g of 3-mercaptopropyltrimethoxysilane, and 10.56 g of AIBN are mixed, and after stirring, charged in a dropping apparatus and taken for 3 hours. It was dripped. After completion of the dropping, the reaction was further continued for 3 hours to obtain an organic polymer A5 having a trimethoxysilyl group, which is a mixture of a polyoxyalkylene polymer, a polyoxyalkylene polymer and a vinyl polymer.
As a result of measuring the molecular weight of the obtained organic polymer A5 having a trimethoxysilyl group by GPC, the peak top molecular weight was 4000 and the molecular weight distribution was 1.6. According to H ¹ -NMR measurement, the number of terminal trimethoxysilyl groups was 2.35 per molecule.

(Synthesis Example 6)
As shown in Table 2, 40.00 g of ethyl acetate, 70.00 g of methyl methacrylate, 2-ethylhexyl methacrylate (Tokyo Chemical Industry Co., Ltd.) were added to a flask equipped with a stirrer, a nitrogen gas inlet tube, a thermometer, and a reflux condenser. )) 30.00 g, 3-methacryloxypropyltrimethoxysilane (trade name: KBM503, manufactured by Shin-Etsu Chemical Co., Ltd.) 12.00 g, and titanocene diclide 0.10 g as a metal catalyst were charged and nitrogen gas was introduced into the flask. The contents of the flask were heated to 80 ° C. while introducing. Next, 4.30 g of 3-mercaptopropyltrimethoxysilane sufficiently substituted with nitrogen gas was added all at once to the flask with stirring. After adding 4.30 g of 3-mercaptopropyltrimethoxysilane, heating and cooling were performed for 4 hours so that the temperature of the contents in the stirring flask could be maintained at 80 ° C. Further, 4.30 g of 3-mercaptopropyltrimethoxysilane sufficiently substituted with nitrogen gas was added to the flask over 5 minutes with stirring. After the additional addition of 4.30 g of 3-mercaptopropyltrimethoxysilane, the reaction was carried out for 4 hours while further cooling and heating so that the temperature of the contents in the stirring flask could be maintained at 90 ° C. . After a total of 8 hours and 5 minutes of reaction, the temperature of the reaction product was returned to room temperature, 20.00 g of a benzoquinone solution (95% THF solution) was added to the reaction product to stop the polymerization, and a vinyl system having a trimethoxysilyl group Polymer A6 was obtained. The peak top molecular weight was 4000, and the molecular weight distribution was 2.4. The number of trimethoxysilyl groups contained by H ¹ -NMR measurement was 2.00 per molecule.

  In Table 2, the compounding quantity of each compounding substance is shown by g. The polyoxyalkylene polymers A1 and A2 are the polyoxyalkylene polymers A1 and A2 obtained in Synthesis Examples 1 and 2, respectively.

(Synthesis Example 7)
As shown in Table 3, to a flask equipped with a stirrer, a nitrogen gas inlet tube, a thermometer, a dropping device and a reflux condenser, 3-aminopropyltrimethoxysilane (trade name: Z-6610, Toray Dow Corning Silicone Co., Ltd. 100 g, 3-glycidoxypropyltrimethoxysilane (trade name: Z-6040, Toray Dow Corning Silicone Co., Ltd.) 276 g was added and stirred at 50 ° C. for 72 hours to give a silane compound B1 was obtained.
About the obtained silane compound B1, the disappearance of the peak due to the epoxy group near 910 cm ⁻¹ was confirmed by FT-IR, the peak of the secondary amine near 1140 cm ⁻¹ was confirmed, and ²⁹ Si-NMR Furthermore, the appearance of a new peak was confirmed from -60 ppm to -70 ppm.

(Synthesis Example 8)
As shown in Table 3, to a flask equipped with a stirrer, a nitrogen gas inlet tube, a thermometer, a dropping device and a reflux condenser, 3-aminopropyltrimethoxysilane (trade name: Z-6610, Toray Dow Corning Silicone Co., Ltd. 100 g, 3-glycidoxypropyltrimethoxysilane (trade name: Z-6040, Toray Dow Corning Silicone Co., Ltd.) 276 g was added, and the mixture was stirred at 23 ° C. for 168 hours. B2 was obtained.
With respect to the obtained silane compound B2, disappearance of a peak due to an epoxy group near 910 cm ⁻¹ was confirmed by FT-IR, and a secondary amine peak near 1140 cm ⁻¹ was confirmed. In addition, no peak was observed from -60 ppm to -70 ppm from ²⁹ Si-NMR.

(Synthesis Example 9)
As shown in Table 3, to a flask equipped with a stirrer, a nitrogen gas inlet tube, a thermometer, a dropping device and a reflux condenser, 3-aminopropyltrimethoxysilane (trade name: Z-6610, Toray Dow Corning Silicone Co., Ltd.) 44.62 g, 3-glycidoxypropyltrimethoxysilane (trade name: Z-6040, Toray Dow Corning Silicone Co., Ltd.) 100 g was added and stirred at 50 ° C. for 72 hours. Silane compound B3 was obtained.
About the obtained silane compound B3, disappearance of a peak due to an epoxy group in the vicinity of 910 cm ⁻¹ was confirmed by FT-IR, a secondary amine peak in the vicinity of 1140 cm ⁻¹ was confirmed, and ²⁹ Si-NMR Furthermore, the appearance of a new peak was confirmed from -60 ppm to -70 ppm.

(Synthesis Example 10)
As shown in Table 3, to a flask equipped with a stirrer, a nitrogen gas inlet tube, a thermometer, a dropping device and a reflux condenser, 3-aminopropyltrimethoxysilane (trade name: Z-6610, Toray Dow Corning Silicone Co., Ltd.) 31.61 g, 3-glycidoxypropyltrimethoxysilane (trade name: Z-6040, Toray Dow Corning Silicone Co., Ltd.) 100 g was added and stirred at 50 ° C. for 72 hours. Silane compound B4 was obtained.
With respect to the obtained silane compound B4, the disappearance of the peak due to the epoxy group near 910 cm ⁻¹ was confirmed by FT-IR, the peak of the secondary amine near 1140 cm ⁻¹ was confirmed, and ²⁹ Si-NMR Furthermore, the appearance of a new peak was confirmed from -60 ppm to -70 ppm.

  In Table 3, the compounding quantity of each compounding substance is shown by g.

(Comparative Synthesis Example 1)
As shown in Table 4, to a flask equipped with a stirrer, a nitrogen gas inlet tube, a thermometer, a dropping device and a reflux condenser, N-2- (aminoethyl) -3-aminopropyltrimethoxysilane (trade name: KBM603, manufactured by Shin-Etsu Chemical Co., Ltd.) 50.00 g, 3-glycidoxypropyltrimethoxysilane 127.5 g were added and stirred at 50 ° C. for 72 hours to obtain a silane compound X1.
The obtained silane compound X1, ^{1410 cm} -1 in FT-IR, to confirm the disappearance of a peak attributable to the amino groups in the vicinity of 1,120 cm ^-1, to confirm the disappearance of the peak due to the epoxy group in the vicinity of 910 cm ^-1 . In addition, no peak was observed from -60 ppm to -70 ppm from ²⁹ Si-NMR.

(Comparative Synthesis Example 2)
As shown in Table 4, to a flask equipped with a stirrer, a nitrogen gas inlet tube, a thermometer, a dropping device and a reflux condenser, 3-aminopropyltrimethoxysilane (trade name: Z-6610, Toray Dow Corning Silicone Co., Ltd. (10.00 g), 3-glycidoxypropyltrimethoxysilane (trade name: Z-6040, Toray Dow Corning Silicone Co., Ltd.) (15.82 g) was added, and the mixture was stirred at 50 ° C. for 72 hours. Silane compound X2 was obtained.
About the obtained silane compound X2, the disappearance of the peak due to the epoxy group near 910 cm ⁻¹ was confirmed by FT-IR, the peak of the secondary amine near 1140 cm ⁻¹ was confirmed, and ²⁹ Si-NMR Furthermore, the appearance of a new peak was confirmed from -60 ppm to -70 ppm.

(Comparative Synthesis Example 3)
As shown in Table 4, to a flask equipped with a stirrer, a nitrogen gas inlet tube, a thermometer, a dropping device and a reflux condenser, 3-aminopropyltrimethoxysilane (trade name: Z-6610, Toray Dow Corning Silicone Co., Ltd.) 10.00 g, 3-glycidoxypropyltrimethoxysilane (trade name: Z-6040, Toray Dow Corning Silicone Co., Ltd.) 158.20 g was added and stirred at 50 ° C. for 72 hours. Silane compound X3 was obtained.
About the obtained silane compound X3, disappearance of a peak due to an epoxy group in the vicinity of 910 cm ⁻¹ was confirmed by FT-IR, and a peak of a secondary amine in the vicinity of 1140 cm ⁻¹ was confirmed. ²⁹ Si-NMR Furthermore, the appearance of a new peak was confirmed from -60 ppm to -70 ppm.

  In Table 4, the compounding quantity of each compounding substance is shown by g.

(Synthesis Example 11)
As shown in Table 5, 100 g of the silane compound B1 obtained in Synthesis Example 7 was placed in a flask equipped with a stirrer, a nitrogen gas inlet tube, a thermometer, a dropping device, and a reflux condenser, followed by Olgatrix TC-750. 63.1 g of [trade name, titanium diisopropoxybis (ethyl acetoacetate) manufactured by Matsumoto Fine Chemical Co., Ltd.] was added and aged by heating and stirring at 70 ° C. for 144 hours to obtain a titanium catalyst G1. About the obtained titanium catalyst G1, the change of the peak was confirmed from ²⁹ Si-NMR.

(Synthesis Example 12)
As shown in Table 5, 100 g of the silane compound B1 obtained in Synthesis Example 7 was placed in a flask equipped with a stirrer, a nitrogen gas inlet tube, a thermometer, a dropping device, and a reflux condenser, followed by Olgatrix TC-750. Was aged by heating and stirring at 70 ° C. for 144 hours to obtain a titanium catalyst G2. About the obtained titanium catalyst G2, the change of the peak was confirmed from ²⁹ Si-NMR.

(Synthesis Example 13)
A flask equipped with a stirrer, a nitrogen gas inlet tube, a thermometer, a dropping device and a reflux condenser was charged with 23.47 g of triethylamine, 10 g of titanium tetrachloride, and subsequently 17.19 g of t-butyl alcohol. The mixture was stirred at room temperature for 2 hours, and the precipitate was filtered and purified by distillation to obtain titanium tetra-t-butoxide. 10 g of the obtained titanium tetra-t-butoxide and 7.65 g of ethyl acetoacetate (manufactured by Nippon Gosei Co., Ltd.) were added and stirred at room temperature for 2 hours, and then stirred at 70 ° C. for 2 hours. After completion of the reaction, unreacted substances and the like were removed under reduced pressure to obtain a titanium catalyst C1.

Subsequently, as shown in Table 5, 19.85 g of the silane compound B1 obtained in Synthesis Example 7 was added to 14.12 g of the obtained titanium catalyst C1 and aged by heating and stirring at 50 ° C. for 72 hours. A titanium catalyst G3 was obtained. About the obtained titanium catalyst G3, the change of the peak was confirmed from ²⁹ Si-NMR.

(Synthesis Example 14)
In a flask equipped with a stirrer, a nitrogen gas inlet tube, a thermometer, a dropping device, and a reflux condenser, 50 g of titanium tetraisopropoxide (trade name: Orgatics TA-10, manufactured by Matsumoto Fine Chemical Co., Ltd.), methylacetate 40.85 g of acetate (manufactured by Nippon Gosei Co., Ltd.) was added, stirred at room temperature for 2 hours, and then stirred at 70 ° C. for 2 hours. After completion of the reaction, unreacted substances and the like were removed under reduced pressure to obtain a titanium catalyst C2.

Subsequently, as shown in Table 5, 106.96 g of the silane compound B1 obtained in Synthesis Example 7 was added to 69.71 g of the obtained titanium catalyst C2, and the mixture was aged by heating and stirring at 60 ° C. for 168 hours. A titanium catalyst G4 was obtained. About the obtained titanium catalyst G4, the change of the peak was confirmed from ²⁹ Si-NMR.

(Synthesis Example 15)
50 g of titanium tetraisopropoxide and 50.72 g of isopropyl acetoacetate (manufactured by Nihon Gosei Co., Ltd.) are placed in a flask equipped with a stirrer, a nitrogen gas inlet tube, a thermometer, a dripping device, and a reflux condenser. The mixture was stirred for 2 hours and then stirred at 70 ° C. for 2 hours. After completion of the reaction, unreacted substances and the like were removed under reduced pressure to obtain a titanium catalyst C3.

Subsequently, as shown in Table 5, 79.58 g of the obtained titanium catalyst C3 was charged with 118.85 g of the silane compound B1 obtained in Synthesis Example 7, and aged by heating and stirring at 70 ° C. for 72 hours. Catalyst G5 was obtained. About the obtained titanium catalyst G5, the change of the peak was confirmed from ²⁹ Si-NMR.

(Synthesis Example 16)
As shown in Table 5, 118.85 g of the silane compound B2 obtained in Synthesis Example 8 was added to a flask equipped with a stirrer, a nitrogen gas inlet tube, a thermometer, a dropping device, and a reflux condenser. Name: KBM1003, manufactured by Shin-Etsu Chemical Co., Ltd.) (3.8 g) and ORGATICS TC-750 (78.88 g) were added and aged by heating and stirring at 70 ° C. for 144 hours to obtain a titanium catalyst G6. About the obtained titanium catalyst G6, the change of the peak was confirmed from ²⁹ Si-NMR.

(Synthesis Example 17)
As shown in Table 5, 184.28 g of the silane compound B2 obtained in Synthesis Example 8 and ORGATICS TC-750 were added to a flask equipped with a stirrer, a nitrogen gas inlet tube, a thermometer, a dropping device, and a reflux condenser. 100.00 g was added and aged by heating and stirring at 70 ° C. for 144 hours to obtain a titanium catalyst G7. About the obtained titanium catalyst G7, the change of the peak was confirmed from ²⁹ Si-NMR.

(Synthesis Example 18)
As shown in Table 5, 126.93 g of the silane compound B3 obtained in Synthesis Example 9 and ORGATICS TC-750 were added to a flask equipped with a stirrer, a nitrogen gas inlet tube, a thermometer, a dropping device, and a reflux condenser. 100.00 g was added and aged by heating and stirring at 70 ° C. for 144 hours to obtain a titanium catalyst G8. About the obtained titanium catalyst G8, the change of the peak was confirmed from ²⁹ Si-NMR.

(Synthesis Example 19)
As shown in Table 5, 156.37 g of the silane compound B4 obtained in Synthesis Example 10 and ORGATICS TC-750 were added to a flask equipped with a stirrer, a nitrogen gas inlet tube, a thermometer, a dropping device, and a reflux condenser. 100.00 g was added and matured by heating and stirring at 70 ° C. for 144 hours to obtain a titanium catalyst G9. About the obtained titanium catalyst G9, the change of the peak was confirmed from ²⁹ Si-NMR.

In Table 5, the compounding quantity of each compounding substance is shown by g. Silane compounds B1 to B4 are silane compounds B1 to B4 obtained in Synthesis Examples 7 to 10, respectively, and titanium catalysts C1 to C3 are titanium catalysts C1 to C3 obtained in Synthesis Examples 13 to 15, respectively. The details are as follows.
ORGATICS TC-750: trade name, titanium diisopropoxybis (ethyl acetoacetate) manufactured by Matsumoto Fine Chemical Co., Ltd.
Vinyltrimethoxysilane: Trade name: KBM1003, manufactured by Shin-Etsu Chemical Co., Ltd.

(Synthesis Example 20)
As shown in Table 6, in a flask equipped with a stirrer, nitrogen gas inlet tube, thermometer, dropping device and reflux condenser, 10 g of the silane compound B1 obtained in Synthesis Example 7 and 40 g of Olgax TC-750 were added. The mixture was aged by heating and stirring at 70 ° C. for 144 hours to obtain a titanium catalyst G10. About the obtained titanium catalyst G10, the change of the peak was confirmed from ²⁹ Si-NMR.

(Synthesis Example 21)
As shown in Table 6, in a flask equipped with a stirrer, nitrogen gas inlet tube, thermometer, dropping device, and reflux condenser, 60 g of the silane compound B1 obtained in Synthesis Example 7 and 40 g of Olgax TC-750 were added. After aging by heating and stirring at 70 ° C. for 144 hours, 100 g of normal paraffin (trade name: N-11, manufactured by JX Nippon Oil & Energy Corporation) is added and heated and stirred at 70 ° C. for 144 hours. To obtain a titanium catalyst G11. About the obtained titanium catalyst G11, the change of the peak was confirmed from ²⁹ Si-NMR.

(Synthesis Example 22)
As shown in Table 6, a titanium catalyst G12 was obtained by the same method as in Synthesis Example 21 except that the blending ratio of the blended materials was changed. About the obtained titanium catalyst G12, the change of the peak was confirmed from ²⁹ Si-NMR.

(Synthesis Example 23)
As shown in Table 6, 10 g of the silane compound B1 obtained in Synthesis Example 7 was added to a flask equipped with a stirrer, a nitrogen gas inlet tube, a thermometer, a dropping device, and a reflux condenser, and (D) 50 g of methoxysilane (trade name: KBM103, manufactured by Shin-Etsu Chemical Co., Ltd.), 40 g of ORGATICS TC-750 and 100 g of normal paraffin were added and aged by heating and stirring at 70 ° C. for 144 hours, titanium catalyst G13 Got. About the obtained titanium catalyst G13, the change of the peak was confirmed from ²⁹ Si-NMR.

(Synthesis Example 24)
As shown in Table 6, a titanium catalyst G14 was obtained by the same method as in Synthesis Example 23, except that the blending ratio of the blended materials was changed. About the obtained titanium catalyst G14, the change of the peak was confirmed from ²⁹ Si-NMR.

(Synthesis Examples 25 to 28)
As shown in Table 6, titanium catalysts G15 to G18 were obtained in the same manner as in Synthesis Example 24 except that (D) the silane compound was changed. About the obtained titanium catalysts G15-G18, the change of the peak was confirmed from ²⁹ Si-NMR.

(Synthesis Example 29)
As shown in Table 6, 10 g of the silane compound B1 obtained in Synthesis Example 7 was added to a flask equipped with a stirrer, a nitrogen gas inlet tube, a thermometer, a dropping device, and a reflux condenser, and (D) 50 g of methoxysilane (trade name: KBM103, manufactured by Shin-Etsu Chemical Co., Ltd.) is added, followed by 40 g of ORGATICS TC-750, aging by heating and stirring at 70 ° C. for 144 hours, and then 100 g of normal paraffin. The mixture was aged by heating and stirring at 70 ° C. for 144 hours to obtain a titanium catalyst G19. About the obtained titanium catalyst G19, the change of the peak was confirmed from ²⁹ Si-NMR.

(Synthesis Example 30)
As shown in Table 6, in a flask equipped with a stirrer, nitrogen gas inlet tube, thermometer, dropping device and reflux condenser, 10 g of the silane compound B1 obtained in Synthesis Example 7 and 40 g of Olgax TC-750 were added. The mixture was aged by heating and stirring at 70 ° C. for 144 hours, and (D) 50 g of phenyltrimethoxysilane (trade name: KBM103, manufactured by Shin-Etsu Chemical Co., Ltd.) as a silane compound and 100 g of normal paraffin were added. The mixture was aged by heating and stirring at 144 ° C. for 144 hours to obtain a titanium catalyst G20. About the obtained titanium catalyst G20, the change of the peak was confirmed from ²⁹ Si-NMR.

(Synthesis Example 31)
As shown in Table 6, a titanium catalyst G21 was obtained in the same manner as in Synthesis Example 29 except that the blending ratio of the blended materials was changed. About the obtained titanium catalyst G21, the change of the peak was confirmed from ²⁹ Si-NMR.

In Table 6, the compounding quantity of each compounding substance is shown by g. Silane compound B1 is silane compound B1 obtained in Synthesis Example 7, and details of other compounding substances are as follows.
ORGATICS TC-750: trade name, titanium diisopropoxybis (ethyl acetoacetate) manufactured by Matsumoto Fine Chemical Co., Ltd.
Phenyltrimethoxysilane: Trade name: KBM-103, manufactured by Shin-Etsu Chemical Co., Ltd.
Vinyltrimethoxysilane: Trade name: KBM-1003, manufactured by Shin-Etsu Chemical Co., Ltd.
Methyltrimethoxysilane: Trade name: KBM-13, manufactured by Shin-Etsu Chemical Co., Ltd.
3-glycidoxypropyltrimethoxysilane: Trade name: KBM-403, manufactured by Shin-Etsu Chemical Co., Ltd.
Decyltrimethoxysilane: Trade name: KBM-3013C, manufactured by Shin-Etsu Chemical Co., Ltd.

Example 1
As shown in Table 7, 50 g of the polyoxyalkylene polymer A1 obtained in Synthesis Example 1 and Synthesis Example 2 were placed in a 300 mL flask equipped with a stirrer, thermometer, nitrogen inlet, monomer charging tube, and water-cooled condenser. 10 g of the polyoxyalkylene polymer A2 obtained in the above and 40 g of vinyl polymer A4 obtained in Synthesis Example 4 in terms of solid content were mixed. The mixture was heated (120 ° C.) and degassed under reduced pressure to remove residual monomer and m-xylene contained in the vinyl polymer A4, and cooled to room temperature. Thereafter, 16.5 g of the titanium catalyst G2 obtained in Synthesis Example 12 was added and degassed and stirred at 25 ° C. to obtain a curable composition. Table 8 shows the results of the curability test, the storage stability test, the surface curability test, and the adhesion test of the curable composition.

(Example 2)
As shown in Table 7, 50 g of the polyoxyalkylene polymer A1 obtained in Synthesis Example 1 and Synthesis Example 2 were placed in a 300 mL flask equipped with a stirrer, thermometer, nitrogen inlet, monomer charging tube, and water-cooled condenser. 10 g of the polyoxyalkylene polymer A2 obtained in the above and 40 g of vinyl polymer A3 obtained in Synthesis Example 3 in terms of solid content were mixed. The mixture was heated (120 ° C.) and degassed under reduced pressure to remove residual monomers and ethyl acetate contained in the vinyl polymer A3, and cooled to room temperature. Thereafter, 11.0 g of the titanium catalyst G3 obtained in Synthesis Example 13 was added and degassed and stirred at 25 ° C. to obtain a curable composition. Table 8 shows the results of the curability test, the storage stability test, the surface curability test, and the adhesion test of the curable composition.

(Example 3)
As shown in Table 7, 50 g of the polyoxyalkylene polymer A1 obtained in Synthesis Example 1 and Synthesis Example 2 were placed in a 300 mL flask equipped with a stirrer, thermometer, nitrogen inlet, monomer charging tube, and water-cooled condenser. 10 g of the polyoxyalkylene polymer A2 obtained in the above and 40 g of vinyl polymer A3 obtained in Synthesis Example 3 in terms of solid content were mixed. The mixture was heated (120 ° C.) and degassed under reduced pressure to remove residual monomers and ethyl acetate contained in the vinyl polymer A3, and cooled to room temperature. Thereafter, 9.0 g of the titanium catalyst G4 obtained in Synthesis Example 14 was added and degassed and stirred at 25 ° C. to obtain a curable composition. Table 8 shows the results of the curability test, the storage stability test, the surface curability test, and the adhesion test of the curable composition.

Example 4
As shown in Table 7, 50 g of the polyoxyalkylene polymer A1 obtained in Synthesis Example 1 and Synthesis Example 2 were placed in a 300 mL flask equipped with a stirrer, thermometer, nitrogen inlet, monomer charging tube, and water-cooled condenser. 10 g of the polyoxyalkylene polymer A2 obtained in the above and 40 g of vinyl polymer A3 obtained in Synthesis Example 3 in terms of solid content were mixed. The mixture was heated (120 ° C.) and degassed under reduced pressure to remove residual monomers and ethyl acetate contained in the vinyl polymer A3, and cooled to room temperature. Thereafter, 11.0 g of the titanium catalyst G5 obtained in Synthesis Example 15 was added, and degassed and stirred at 25 ° C. to obtain a curable composition. Table 8 shows the results of the curability test, the storage stability test, the surface curability test, and the adhesion test of the curable composition.

(Example 5)
As shown in Table 7, 50 g of the polyoxyalkylene polymer A1 obtained in Synthesis Example 1 and Synthesis Example 2 were placed in a 300 mL flask equipped with a stirrer, thermometer, nitrogen inlet, monomer charging tube, and water-cooled condenser. 10 g of the polyoxyalkylene polymer A2 obtained in the above and 40 g of vinyl polymer A3 obtained in Synthesis Example 3 in terms of solid content were mixed. The mixture was heated (120 ° C.) and degassed under reduced pressure to remove residual monomers and ethyl acetate contained in the vinyl polymer A3, and cooled to room temperature. Thereafter, 9.0 g of the titanium catalyst G6 obtained in Synthesis Example 16 was added and degassed and stirred at 25 ° C. to obtain a curable composition. Table 8 shows the results of the curability test, the storage stability test, the surface curability test, and the adhesion test of the curable composition.

(Example 6)
As shown in Table 7, 100 g of the polymer A5 obtained in Synthesis Example 5 was added to a 300 mL flask equipped with a stirrer, thermometer, nitrogen inlet, monomer charging tube, and water-cooled condenser, and (E) surface-treated calcium carbonate. MC coating P-1 50g, Disparon # 6500 1g as a thixotropic agent, 1g Nocrack CD 1% as an anti-aging agent, heated (100 ° C), degassed and stirred for 1 hour until room temperature (25 ° C) Then, 5 g of acetyltriethyl citrate as a diluent (F) and 10 g of the titanium catalyst G1 obtained in Synthesis Example 11 were added and further deaerated and stirred to obtain a curable composition. Table 8 shows the results of the curability test, the storage stability test, the surface curability test, and the adhesion test of the curable composition.

(Example 7)
As shown in Table 7, 100 g of the polymer A5 obtained in Synthesis Example 5 and titanium obtained in Synthesis Example 17 were placed in a 300 mL flask equipped with a stirrer, thermometer, nitrogen inlet, monomer charging tube, and water-cooled condenser. 10.0 g of catalyst G7 was added and degassed and stirred at 25 ° C. to obtain a curable composition. Table 8 shows the results of the curability test, the storage stability test, the surface curability test, and the adhesion test of the curable composition.

(Example 8)
As shown in Table 7, 100 g of the polymer A5 obtained in Synthesis Example 5 and titanium obtained in Synthesis Example 18 were placed in a 300 mL flask equipped with a stirrer, thermometer, nitrogen inlet, monomer charging tube, and water-cooled condenser. 9.0 g of catalyst G8 was added and degassed and stirred at 25 ° C. to obtain a curable composition. Table 8 shows the results of the curability test, the storage stability test, the surface curability test, and the adhesion test of the curable composition.

Example 9
As shown in Table 7, 100 g of the polymer A5 obtained in Synthesis Example 5 and titanium obtained in Synthesis Example 19 were placed in a 300 mL flask equipped with a stirrer, thermometer, nitrogen inlet, monomer charging tube, and water-cooled condenser. 9.0 g of catalyst G9 was added and degassed and stirred at 25 ° C. to obtain a curable composition. Table 8 shows the results of the curability test, the storage stability test, the surface curability test, and the adhesion test of the curable composition.

In Table 7, the compounding quantity of each compounding substance is shown by g, and polymer A3 and A4 are shown by the compounding quantity of solid content conversion. The polymers A1 to A2 are the polyoxyalkylene polymers A1 to A2 obtained in Synthesis Examples 1 and 2, respectively, and the polymers A3 to A4 are vinyl polymers A3 to A4 obtained in Synthesis Examples 3 to 4, respectively. The polymer A5 is the organic polymer A5 obtained in Synthesis Example 5, and the titanium catalysts G1 to G9 are the titanium catalysts G1 to G9 obtained in Synthesis Examples 11 to 19, respectively. Details of other compounding substances are as follows.
MC coat P-1: trade name, colloidal calcium carbonate, surface paraffin wax treatment manufactured by Shiroishi Kogyo Co., Ltd.
Disparon # 6500: trade name, amide wax, manufactured by Enomoto Kasei Co., Ltd.
NOCRACK CD: trade name, 4,4′-bis (α, α-dimethylbenzyl) diphenylamine, manufactured by Ouchi Shinko Co., Ltd.
Acetyltriethyl citrate: manufactured by Tokyo Chemical Industry Co., Ltd.

(Example 10)
As shown in Table 9, 100 g of the polyoxyalkylene polymer A1 obtained in Synthesis Example 1 and Synthesis Example 7 were placed in a 300 mL flask equipped with a stirrer, thermometer, nitrogen inlet, monomer charging tube, and water-cooled condenser. 6 g of the silane compound B1 obtained in step 4 and 4 g of ORGATICS TC-750 were added and stirred at 25 ° C. to obtain a curable composition. Table 10 shows the results of the storage stability test, curability test, surface curability test, and adhesion test of the curable composition.

(Example 11)
As shown in Table 9, 50 g of the polyoxyalkylene polymer A1 obtained in Synthesis Example 1 and Synthesis Example 2 were placed in a 300 mL flask equipped with a stirrer, a thermometer, a nitrogen inlet, a monomer charging tube and a water-cooled condenser. 10 g of the polyoxyalkylene polymer A2 obtained in the above and 40 g of vinyl polymer A3 obtained in Synthesis Example 3 in terms of solid content were mixed. The mixture was heated (120 ° C.) and degassed under reduced pressure to remove residual monomers and ethyl acetate contained in the vinyl polymer A3, and cooled to room temperature. Thereafter, 6 g of the silane compound B1 obtained in Synthesis Example 7 and 4 g of ORGATIC TC-750 were added, and the mixture was deaerated and stirred at 25 ° C. to obtain a curable composition. Table 10 shows the results of the storage stability test, curability test, surface curability test, and adhesion test of the curable composition.

(Example 12)
As shown in Table 9, 50 g of the polyoxyalkylene polymer A1 obtained in Synthesis Example 1 and Synthesis Example 2 were placed in a 300 mL flask equipped with a stirrer, a thermometer, a nitrogen inlet, a monomer charging tube and a water-cooled condenser. 10 g of the polyoxyalkylene polymer A2 obtained in the above and 40 g of vinyl polymer A3 obtained in Synthesis Example 3 in terms of solid content were mixed. The mixture was heated (120 ° C.) and degassed under reduced pressure to remove residual monomers and ethyl acetate contained in the vinyl polymer A3, and cooled to room temperature. Thereafter, 6 g of the silane compound B2 obtained in Synthesis Example 8 and 4 g of ORGATIC TC-750 were added, and the mixture was deaerated and stirred at 25 ° C. to obtain a curable composition. Table 10 shows the results of the storage stability test, curability test, surface curability test, and adhesion test of the curable composition.

  In Table 9, the compounding quantity of each compounding substance is shown by g, and polymer A3 is shown by the compounding quantity of solid content conversion. The polymers A1 to A2 are the polyoxyalkylene polymers A1 to A2 obtained in Synthesis Examples 1 and 2, respectively, the polymer A3 is the vinyl polymer A3 obtained in Synthesis Example 3, and the silane compounds B1 to B2 Are silane compounds B1 to B2 obtained in Synthesis Examples 7 to 8, respectively, and Olgatyx TC-750 is a trade name, titanium diisopropoxybis (ethyl acetoacetate) manufactured by Matsumoto Fine Chemical Co., Ltd.

(Comparative Example 1)
As shown in Table 11, 100 g of the polyoxyalkylene polymer A1 obtained in Synthesis Example 1 and Olgax TC were placed in a 300 mL flask equipped with a stirrer, thermometer, nitrogen inlet, monomer charging tube and water-cooled condenser. 4g of -750 was put and deaerated and stirred at 25 ° C to obtain a curable composition. Table 12 shows the results of the curability test, the storage stability test, the surface curability test, and the adhesion test of the curable composition.

(Comparative Example 2)
As shown in Table 11, 50 g of the polyoxyalkylene polymer A1 obtained in Synthesis Example 1 and Synthesis Example 2 were placed in a 300 mL flask equipped with a stirrer, a thermometer, a nitrogen inlet, a monomer charging tube, and a water-cooled condenser. 10 g of the polyoxyalkylene polymer A2 obtained in the above and 40 g of vinyl polymer A3 obtained in Synthesis Example 3 in terms of solid content were mixed. The mixture was heated (120 ° C.) and degassed under reduced pressure to remove residual monomers and ethyl acetate contained in the vinyl polymer A3, and cooled to room temperature. Thereafter, 3 g of 3-glycidoxypropyltrimethoxysilane and 4 g of Orgatics TC-750 were added and degassed and stirred at 25 ° C. to obtain a curable composition. Table 12 shows the results of the curability test, the storage stability test, the surface curability test, and the adhesion test of the curable composition.

(Comparative Example 3)
As shown in Table 11, 50 g of the polyoxyalkylene polymer A1 obtained in Synthesis Example 1 and Synthesis Example 2 were placed in a 300 mL flask equipped with a stirrer, a thermometer, a nitrogen inlet, a monomer charging tube, and a water-cooled condenser. 10 g of the polyoxyalkylene polymer A2 obtained in the above and 40 g of vinyl polymer A3 obtained in Synthesis Example 3 in terms of solid content were mixed. The mixture was heated (120 ° C.) and degassed under reduced pressure to remove residual monomers and ethyl acetate contained in the vinyl polymer A3, and cooled to room temperature. Then, 5 g of QS-20 was added, heated and degassed and stirred at 100 ° C., returned to room temperature (25 ° C.), 3 g of 3-glycidoxypropyltrimethoxysilane and 4 g of Olgatics TC-750 were added, and degassed at 25 ° C. Air-stirred to obtain a curable composition. Table 12 shows the results of the curability test, the storage stability test, the surface curability test, and the adhesion test of the curable composition.

(Comparative Example 4)
As shown in Table 11, in a 300 mL flask equipped with a stirrer, a thermometer, a nitrogen inlet, a monomer charging tube, and a water-cooled condenser, 50 g of the polyoxyalkylene polymer A1 obtained in Synthesis Example 1 was used in Synthesis Example 2. 10 g of the obtained polyoxyalkylene polymer A2 and 40 g of vinyl polymer A3 obtained in Synthesis Example 3 in terms of solid content were mixed. The mixture was heated (120 ° C.) and degassed under reduced pressure to remove residual monomers and ethyl acetate contained in the vinyl polymer A3, and cooled to room temperature. Thereafter, 50 g of Ryton A-5 was added and heated and deaerated and stirred at 100 ° C. After returning to room temperature (25 ° C.), 6 g of the silane compound X1 obtained in Comparative Synthesis Example 1 and 4 g of Orgatics TC-750 were added and degassed and stirred at 25 ° C. to obtain a curable composition. Table 12 shows the results of the curability test, the storage stability test, the surface curability test, and the adhesion test of the curable composition.

(Comparative Example 5)
As shown in Table 11, in a 300 mL flask equipped with a stirrer, a thermometer, a nitrogen inlet, a monomer charging tube, and a water-cooled condenser, 50 g of the polyoxyalkylene polymer A1 obtained in Synthesis Example 1 was used in Synthesis Example 2. 10 g of the obtained polyoxyalkylene polymer A2 and 40 g of vinyl polymer A3 obtained in Synthesis Example 3 in terms of solid content were mixed. The mixture was heated (120 ° C.) and degassed under reduced pressure to remove residual monomers and ethyl acetate contained in the vinyl polymer A3, and cooled to room temperature. Thereafter, 6 g of the silane compound X2 obtained in Comparative Synthesis Example 2 and 4 g of Orgatics TC-750 were put into 4 g, and deaerated and stirred at 25 ° C. to obtain a curable composition. Table 12 shows the results of the curability test, the storage stability test, the surface curability test, and the adhesion test of the curable composition.

(Comparative Example 6)
As shown in Table 11, in a 300 mL flask equipped with a stirrer, a thermometer, a nitrogen inlet, a monomer charging tube, and a water-cooled condenser, 50 g of the polyoxyalkylene polymer A1 obtained in Synthesis Example 1 was used in Synthesis Example 2. 10 g of the obtained polyoxyalkylene polymer A2 and 40 g of vinyl polymer A3 obtained in Synthesis Example 3 in terms of solid content were mixed. The mixture was heated (120 ° C.) and degassed under reduced pressure to remove residual monomers and ethyl acetate contained in the vinyl polymer A3, and cooled to room temperature. Then, it put in and heated and degassed and stirred at 100 ° C. After returning to room temperature (25 ° C.), 6 g of the silane compound X3 obtained in Comparative Synthesis Example 3 and 4 g of Orgatics TC-750 were added and degassed and stirred at 25 ° C. to obtain a curable composition. Table 12 shows the results of the curability test, the storage stability test, the surface curability test, and the adhesion test of the curable composition.

In Table 11, the compounding quantity of each compounding substance is shown by g, and polymer A3 is shown by the compounding quantity of solid content conversion. The polymers A1 to A2 are the polyoxyalkylene polymers A1 to A2 obtained in Synthesis Examples 1 and 2, respectively, the polymer A3 is the vinyl polymer A3 obtained in Synthesis Example 3, and the silane compounds X1 to X3. Are silane compounds X1 to X3 obtained in Comparative Synthesis Examples 1 to 3, respectively, and details of other compounding substances are as follows.
QS-20: Tokuyama Co., Ltd. trade name, primary particle size 5 to 50 μm, surface-untreated hydrophilic dry silica.
Ryton A-5: trade name manufactured by Shiroishi Kogyo Co., Ltd., ground calcium carbonate, surface fatty acid treatment.
ORGATICS TC-750: trade name, titanium diisopropoxybis (ethyl acetoacetate) manufactured by Matsumoto Fine Chemical Co., Ltd.

(Example 13)
As shown in Table 13, in a 300 mL flask equipped with a stirrer, thermometer, nitrogen inlet, monomer charging tube, and water-cooled condenser, 45 g of the polyoxyalkylene polymer A1 obtained in Synthesis Example 1 was synthesized. 20 g of the polyoxyalkylene polymer A2 obtained in the above and 35 g of vinyl polymer A6 obtained in Synthesis Example 6 in terms of solid content were mixed. The mixture was heated (120 ° C.) and degassed under reduced pressure to remove residual monomers and ethyl acetate contained in the vinyl polymer A6, and cooled to room temperature. Thereafter, 1 g of the silane compound B1 obtained in Synthesis Example 7 and 4 g of ORGATIC TC-750 were added, and the mixture was deaerated and stirred at 25 ° C. to obtain a curable composition. Table 14 shows the results of the storage stability test, the curability test, and the surface curability test of the curable composition.

(Example 14)
A curable composition was prepared in the same manner as in Example 13 except that the blending ratio of the blended materials was changed as shown in Table 13. Table 14 shows the results of the storage stability test, the curability test, and the surface curability test of the curable composition.

(Example 15)
As shown in Table 13, in a 300 mL flask equipped with a stirrer, thermometer, nitrogen inlet, monomer charging tube, and water-cooled condenser, 45 g of the polyoxyalkylene polymer A1 obtained in Synthesis Example 1 was synthesized. 20 g of the polyoxyalkylene polymer A2 obtained in the above and 35 g of vinyl polymer A6 obtained in Synthesis Example 6 in terms of solid content were mixed. The mixture was heated (120 ° C.) and degassed under reduced pressure to remove residual monomers and ethyl acetate contained in the vinyl polymer A6, and cooled to room temperature. Thereafter, 5 g of the titanium catalyst G10 obtained in Synthesis Example 20 was added and degassed and stirred at 25 ° C. to obtain a curable composition. Table 14 shows the results of the storage stability test, the curability test, and the surface curability test of the curable composition.

(Example 16)
As shown in Table 13, in a 300 mL flask equipped with a stirrer, thermometer, nitrogen inlet, monomer charging tube, and water-cooled condenser, 45 g of the polyoxyalkylene polymer A1 obtained in Synthesis Example 1 was synthesized. 20 g of the polyoxyalkylene polymer A2 obtained in the above and 35 g of vinyl polymer A6 obtained in Synthesis Example 6 in terms of solid content were mixed. The mixture was heated (120 ° C.) and degassed under reduced pressure to remove residual monomers and ethyl acetate contained in the vinyl polymer A6, and cooled to room temperature. Thereafter, 5 g of the titanium catalyst G10 obtained in Synthesis Example 20 and 5 g of phenyltrimethoxysilane were added, and the mixture was deaerated and stirred at 25 ° C. to obtain a curable composition. Table 14 shows the results of the storage stability test, the curability test, and the surface curability test of the curable composition.

(Examples 17 to 19)
A curable composition was prepared in the same manner as in Example 16 except that (D) the silane compound was changed as shown in Table 13. Table 14 shows the results of the storage stability test, the curability test, and the surface curability test of the curable composition.

In Table 13, the compounding quantity of each compounding substance is shown by g, and the polymer A6 is shown by the compounding quantity of solid content conversion. The polymers A1 to A2 are the polyoxyalkylene polymers A1 to A2 obtained in Synthesis Examples 1 and 2, respectively, the polymer A6 is the vinyl polymer A6 obtained in Synthesis Example 6, and the silane compound B1 is synthesized. It is the silane compound B1 obtained in Example 7, the titanium catalyst G10 is the titanium catalyst G10 obtained in Synthesis Example 20, and details of other compounding materials are as follows.
ORGATICS TC-750: trade name, titanium diisopropoxybis (ethyl acetoacetate) manufactured by Matsumoto Fine Chemical Co., Ltd.
Phenyltrimethoxysilane: Trade name: KBM-103, manufactured by Shin-Etsu Chemical Co., Ltd.
Vinyltrimethoxysilane: Trade name: KBM-1003, manufactured by Shin-Etsu Chemical Co., Ltd.
Decyltrimethoxysilane: Trade name: KBM-3013C, manufactured by Shin-Etsu Chemical Co., Ltd.
Tetraethoxysilane: Trade name: KBE-04, manufactured by Shin-Etsu Chemical Co., Ltd.

(Example 20)
As shown in Table 15, in a 300 mL flask equipped with a stirrer, thermometer, nitrogen inlet, monomer charging tube, and water-cooled condenser, 27 g of the polyoxyalkylene polymer A1 obtained in Synthesis Example 1 was synthesized. 52 g of the polyoxyalkylene polymer A2 obtained in the above and 21 g of vinyl polymer A6 obtained in Synthesis Example 6 were mixed in terms of solid content. The mixture was heated (120 ° C.) and degassed under reduced pressure to remove residual monomers and ethyl acetate contained in the vinyl polymer A6, and cooled to room temperature. Thereafter, 40 g of Whiten SB (manufactured by Shiraishi Calcium Co., Ltd., heavy calcium carbonate, average particle size 2.2 μm), Carlex 300 (manufactured by Maruo Calcium Co., Ltd., fatty acid surface-treated calcium carbonate, primary particle size (electronic) (Microscope) 0.05 μm) was added, heated (100 ° C.), degassed and stirred for 1 hour, returned to room temperature, 20 g of the titanium catalyst G11 obtained in Synthesis Example 21 was charged, degassed and stirred at 25 ° C., A curable composition was obtained. Tables 16 and 17 show the results of the storage stability test, the curability test, and the adhesion test of the curable composition.

(Examples 21 to 27)
As shown in Table 15, a curable composition was prepared in the same manner as in Example 20 except that the titanium catalysts G12 to G18 were used instead of the titanium catalyst G11. Tables 16 and 17 show the results of the storage stability test, the curability test, and the adhesion test of the curable composition.

In Table 15, the compounding quantity of each compounding substance is shown by g, and polymer A6 is shown by the compounding quantity of solid content conversion. The polymers A1 to A2 are the polyoxyalkylene polymers A1 to A2 obtained in Synthesis Examples 1 and 2, respectively, the polymer A6 is the vinyl polymer A6 obtained in Synthesis Example 6, and the titanium catalysts G11 to G18. These are the titanium catalysts G11 to G18 obtained in Synthesis Examples 21 to 28, and details of other compounding substances are as follows.
Whiteon SB: Shiraishi Calcium Co., Ltd., heavy calcium carbonate, average particle size 2.2 μm.
Carlex 300: manufactured by Maruo Calcium Co., Ltd., fatty acid surface-treated calcium carbonate, primary particle diameter (electron microscope) 0.05 μm.
Normal paraffin: Trade name: N-11, manufactured by JX Nippon Oil & Energy Corporation.

(Example 28)
As shown in Table 18, in a 300 mL flask equipped with a stirrer, thermometer, nitrogen inlet, monomer charging tube, and water-cooled condenser, 45 g of the polyoxyalkylene polymer A1 obtained in Synthesis Example 1 was synthesized. 20 g of the polyoxyalkylene polymer A2 obtained in the above and 35 g of vinyl polymer A6 obtained in Synthesis Example 6 in terms of solid content were mixed. The mixture was heated (120 ° C.) and degassed under reduced pressure to remove residual monomers and ethyl acetate contained in the vinyl polymer A6, and cooled to room temperature. Thereafter, (E) 40 g of whiten SB as a filler was added, heated (100 ° C.), degassed and stirred for 1 hour, returned to room temperature, 1 g of the silane compound B1 obtained in Synthesis Example 7, Olgax TC- 4g of 750 was added and deaerated and stirred at 25 ° C to obtain a curable composition. Tables 19 and 20 show the results of the storage stability test, the curability test, and the adhesion test of the curable composition.

(Examples 29 to 33)
As shown in Table 18, a curable composition was prepared in the same manner as in Example 28 except that (E) the filler was changed. Tables 19 and 20 show the results of the storage stability test, the curability test, and the adhesion test of the curable composition.

In Table 18, the compounding quantity of each compounding substance is shown by g, and polymer A6 is shown by the compounding quantity of solid content conversion. The polymers A1 to A2 are the polyoxyalkylene polymers A1 to A2 obtained in Synthesis Examples 1 and 2, respectively, the polymer A6 is the vinyl polymer A6 obtained in Synthesis Example 6, and the silane compound B1 is synthesized. The details of the other compounding materials are as follows in the silane compound B1 obtained in Example 7.
ORGATICS TC-750: trade name, titanium diisopropoxybis (ethyl acetoacetate) manufactured by Matsumoto Fine Chemical Co., Ltd.
Phenyltrimethoxysilane: Trade name: KBM-103, manufactured by Shin-Etsu Chemical Co., Ltd.
Whiteon SB: trade name, heavy calcium carbonate, manufactured by Shiraishi Calcium Co., Ltd., average particle size 2.2 μm.
Carlex 300: trade name manufactured by Maruo Calcium Co., Ltd., fatty acid surface-treated calcium carbonate, primary particle diameter (electron microscope) 0.05 μm.
Calfine 200: trade name manufactured by Maruo Calcium Co., Ltd., fatty acid surface-treated calcium carbonate, primary particle diameter (electron microscope) 0.07 μm.
ViscoExcel-30: trade name manufactured by Shiroishi Kogyo Co., Ltd., fatty acid surface-treated calcium carbonate, primary particle diameter (electron microscope) 0.03 μm.
MS-100M: trade name manufactured by Maruo Calcium Co., Ltd., fatty acid / resin acid surface-treated calcium carbonate, primary particle diameter (electron microscope) 0.05 μm.
MC coat P-1: trade name, colloidal calcium carbonate, surface paraffin wax treatment, average particle diameter of 3.0 μm manufactured by Shiroishi Kogyo Co., Ltd.

(Example 34)
As shown in Table 21, in a 300 mL flask equipped with a stirrer, thermometer, nitrogen inlet, monomer charging tube, and water-cooled condenser, 27 g of the polyoxyalkylene polymer A1 obtained in Synthesis Example 1 was synthesized. 52 g of the polyoxyalkylene polymer A2 obtained in the above and 21 g of vinyl polymer A6 obtained in Synthesis Example 6 were mixed in terms of solid content. The mixture was heated (120 ° C.) and degassed under reduced pressure to remove residual monomers and ethyl acetate contained in the vinyl polymer A6, and cooled to room temperature. Thereafter, (E) 40 g of whiten SB as the filler, 20 g of Carlex 300 as the surface-treated calcium carbonate, and 1 g of NOCRACK CD as the anti-aging agent are added, heated (100 ° C.), degassed and stirred for 1 hour. The temperature was returned to room temperature (25 ° C.), 10 g of the titanium catalyst G20 obtained in Synthesis Example 30 was added, and the mixture was further degassed and stirred to obtain a curable composition. Table 22 shows the results of the curability test and the storage stability test of the curable composition.

(Example 35)
As shown in Table 21, a curable composition was prepared in the same manner as in Example 34 except that the titanium catalyst G19 was used instead of the titanium catalyst G20. Table 22 shows the results of the curability test and the storage stability test of the curable composition.

(Example 36)
As shown in Table 21, in a 300 mL flask equipped with a stirrer, thermometer, nitrogen inlet, monomer charging tube, and water-cooled condenser, 27 g of the polyoxyalkylene polymer A1 obtained in Synthesis Example 1 was synthesized. 52 g of the polyoxyalkylene polymer A2 obtained in the above and 21 g of vinyl polymer A6 obtained in Synthesis Example 6 were mixed in terms of solid content. The mixture was heated (120 ° C.) and degassed under reduced pressure to remove residual monomers and ethyl acetate contained in the vinyl polymer A6, and cooled to room temperature. Thereafter, 150 g of Almorix B316 as aluminum hydroxide and 5 g of NOCRACK CD as an anti-aging agent were added, heated (100 ° C.), degassed and stirred for 1 hour, returned to room temperature (25 ° C.), (F) Diluent As the component (D), 2.5 g of vinyltrimethoxysilane as the component (D) and 9.2 g of the titanium catalyst G21 obtained in Synthesis Example 31 were added and further deaerated and stirred to obtain a curable composition. Table 22 shows the results of the curability test and the storage stability test of the curable composition, and Table 23 shows the results of the adhesion test.

In Table 21, the compounding quantity of each compounding substance is shown by g, and the polymer A6 is shown by the compounding quantity of solid content conversion. The polymers A1 to A2 are the polyoxyalkylene polymers A1 to A2 obtained in Synthesis Examples 1 and 2, respectively, the polymer A6 is the vinyl polymer A6 obtained in Synthesis Example 6, and the titanium catalysts G19 to G21. Are titanium catalysts G19 to G21 obtained in Synthesis Examples 29 to 31, respectively, and details of other compounding substances are as follows.
Vinyltrimethoxysilane: Trade name: KBM-1003, manufactured by Shin-Etsu Chemical Co., Ltd.
Whiteon SB: trade name, heavy calcium carbonate, manufactured by Shiraishi Calcium Co., Ltd., average particle size 2.2 μm.
Carlex 300: trade name manufactured by Maruo Calcium Co., Ltd., fatty acid surface-treated calcium carbonate, primary particle diameter (electron microscope) 0.05 μm.
Armorix B316: trade name, aluminum hydroxide, average particle diameter of 18 μm, manufactured by Armorix Co., Ltd.
Isopar M: trade name, isoparaffin, manufactured by ExxonMobil Co., Ltd.
NOCRACK CD: trade name, 4,4′-bis (α, α-dimethylbenzyl) diphenylamine, manufactured by Ouchi Shinko Co., Ltd.

(Example 37)
As shown in Table 24, 100 g of the polyoxyalkylene polymer A1 obtained in Synthesis Example 1 was added to a 300 mL flask equipped with a stirrer, a thermometer, a nitrogen inlet, a monomer charging tube and a water-cooled condenser, (E) 40 g of Furex (registered trademark) E-2 [manufactured by Tatsumori Co., Ltd., amorphous silica having an average particle size of 6 μm] was added as amorphous silica, mixed at 100 ° C. and 10 mmHg for 1 hour, and then heated to 20 ° C. After cooling, 21.2 g of the titanium catalyst G14 obtained in Synthesis Example 24 was added and vacuum mixed for 10 minutes to obtain a curable composition.
Table 25 shows the results of the storage stability test, the curability test, the surface curability test, the adhesion test and the transparency test of the curable composition.

(Example 38)
As shown in Table 24, 27 g of the polyoxyalkylene polymer A1 obtained in Synthesis Example 1 and Synthesis Example 2 were placed in a 300 mL flask equipped with a stirrer, a thermometer, a nitrogen inlet, a monomer charging tube, and a water-cooled condenser. 52 g of the polyoxyalkylene polymer A2 obtained in the above and 21 g of vinyl polymer A6 obtained in Synthesis Example 6 were mixed in terms of solid content. The mixture was heated (120 ° C.) and degassed under reduced pressure to remove residual monomers and ethyl acetate contained in the vinyl polymer A6, and cooled to room temperature. Thereafter, (E) 20 g of MR13G (manufactured by Soken Chemical Co., Ltd., methacrylic acid ester polymer powder, average particle size of about 1 μm) as the polymer powder, and FTR8100 (manufactured by Mitsui Oil Co., Ltd.) as the refractive index adjuster, 17 g of C5 and C9 copolymer petroleum resin) was mixed at 100 ° C. and 10 mmHg for 1 hour, then cooled to 20 ° C., and 21.2 g of titanium catalyst G14 obtained in Synthesis Example 24 was added and vacuum mixed for 10 minutes. Thus, a curable composition was obtained.

  The amount of FTR8100 is determined by the following method. First, FTR8100 serving as a refractive index adjusting agent is heated and melted to the component (A) at an appropriate ratio, and the refractive index is measured with an Abbe refractometer at 20 ° C. An XY plot of FTR8100 compounding ratio and refractive index is taken. The FTR8100 blending amount that matches the refractive index of the powder serving as the main filler is the blending amount.

  Table 25 shows the results of the storage stability test, the curability test, the surface curability test, the adhesion test and the transparency test of the curable composition.

(Example 39)
As shown in Table 24, a curable composition was prepared in the same manner as in Example 38 except that the compounding substances were changed. Table 25 shows the results of the storage stability test, the curability test, the surface curability test, the adhesion test and the transparency test of the curable composition.

In Table 24, the compounding quantity of each compounding substance is shown by g, and the polymer A6 is shown by the compounding quantity of solid content conversion. Polymers A1 and A2 are the polyoxyalkylene polymers A1 and A2 obtained in Synthesis Examples 1 and 2, respectively, Polymer A6 is the vinyl polymer A6 obtained in Synthesis Example 6, and titanium catalyst G14 is synthesized. The titanium catalyst G14 obtained in Example 24 and details of other compounding materials are as follows.
MR13G: trade name manufactured by Soken Chemical Co., Ltd., methacrylic acid ester polymer powder, average particle size of about 1 μm.
Fuselex (registered trademark) E-2: trade name of Tatsumori Co., Ltd., amorphous silica, average particle size (50% weight average when measuring particle size distribution by laser method): 6 μm.
FTR8100: trade name of Mitsui Oil Co., Ltd., C5 and C9 copolymer petroleum resin.

  As shown in Tables 7 to 10 and 13 to 25, the curable composition of the present invention exhibited sufficient adhesion, storage stability, and curability.

Claims (16)

(A) an organic polymer containing 0.8 or more crosslinkable silicon groups on average in one molecule and the main chain is not polysiloxane;
(B) An epoxysilane compound represented by the following formula (1) and an aminosilane compound represented by the following formula (2) are added in a range of 1.5 to 10 moles with respect to 1 mole of the aminosilane compound. (C) one or more titanium catalysts selected from the group consisting of a titanium chelate represented by the following formula (3) and a titanium chelate represented by the following formula (4),
A curable composition comprising
0.1 to 40 parts by mass of (B) silane compound and 0.1 to 40 parts by mass of (C) titanium catalyst are blended with respect to 100 parts by mass of (A) organic polymer. Curable composition.

(In the formula (1), R ^{1 to} R ³ are each a hydrogen atom or an alkyl group, R ⁴ is an alkylene group or an alkyleneoxyalkylene group, R ⁵ is a monovalent hydrocarbon group, and R ⁶ is An alkyl group, and a is 0, 1 or 2.)

(In the formula (2), R ^{7 to} R ¹² are each a hydrogen atom or an alkyl group, R ¹³ is a monovalent hydrocarbon group, R ¹⁴ is an alkyl group, and b is 0 or 1. )

(In the formula (3), n R ^{21 s} are independently substituted or unsubstituted hydrocarbon groups having 1 to 20 carbon atoms, and 4-n R ^{22 s} are independently hydrogen atoms. Or a substituted or unsubstituted hydrocarbon group having 1 to 20 carbon atoms, wherein 4-n R ²³ and 4-n R ²⁴ are independently substituted or unsubstituted carbon atoms having 1 to 20 carbon atoms. And n is 0, 1, 2 or 3.)

(In the formula (4), R ²⁵ is a substituted or unsubstituted divalent hydrocarbon group having 1 to 20 carbon atoms, and the two R ²⁶ are independently hydrogen atoms or substituted or unsubstituted. And 2 R ²⁷ and 2 R ²⁸ are each independently a substituted or unsubstituted hydrocarbon group having 1 to 20 carbon atoms.)   The curable composition according to claim 1, wherein the (B) silane compound is a silane compound obtained by reacting the epoxysilane compound and the aminosilane compound at a reaction temperature of 40 to 100 ° C.   The (A) organic polymer is a polyoxyalkylene polymer containing 0.8 or more crosslinkable silicon groups on average per molecule, and 0.8 or more crosslinks on average per molecule. Selected from the group consisting of a saturated hydrocarbon polymer containing a functional silicon group and a (meth) acrylic acid ester polymer containing an average of 0.8 or more crosslinkable silicon groups in one molecule. The curable composition according to claim 1 or 2, wherein the curable composition is one or more.   The curable composition according to claim 1, wherein the crosslinkable silicon group contains a trimethoxysilyl group.   (D) The curing according to any one of claims 1 to 4, further comprising a silane compound having one hydrolyzable silicon group and one primary amino group in one molecule. Sex composition. The curable composition according to claim 5, wherein the (D) silane compound is a compound represented by the following formula (12).

(In the formula (12), R ⁴¹ is a methyl group or an ethyl group, and when a plurality of R ⁴¹ are present, they may be the same or different, and R ⁴² is a methyl group. Or when there are a plurality of R ^{42 s} , they may be the same or different, R ⁴³ is a hydrocarbon group having 1 to 10 carbon atoms, and m is 2 Or 3 and n is 0 or 1.)   (E) The curable composition according to any one of claims 1 to 6, further comprising a filler.   The filler (E) is at least one selected from the group consisting of surface-treated calcium carbonate, amorphous silica having a particle size of 0.01 to 300 μm, and polymer powder having a particle size of 0.01 to 300 μm. The curable composition according to claim 7.   The curable composition according to claim 8, wherein the difference between the refractive index of the organic polymer (A) and the refractive index of the amorphous silica is 0.1 or less.   The curability according to claim 8 or 9, wherein the difference between the refractive index of the liquid phase component (A) containing the organic polymer as a main component and the refractive index of the polymer powder is 0.1 or less. Composition.   By adding a refractive index adjusting agent to the (A) organic polymer, the difference between the refractive index of the liquid phase component mainly composed of the (A) organic polymer and the refractive index of the polymer powder is 0.1. It is set as follows, The curable composition of Claim 10 characterized by the above-mentioned.   The polymer powder polymerizes a monomer selected from the group consisting of (meth) acrylic acid ester, vinyl acetate, ethylene and vinyl chloride alone, or the monomer and one or more vinyl monomers The curable composition according to any one of claims 8 to 11, which is a polymer powder obtained from a polymer obtained by copolymerization.   The curable composition according to claim 12, wherein the polymer powder is at least one selected from the group consisting of an acrylic polymer powder and a vinyl polymer powder.   (F) The curable composition according to any one of claims 1 to 13, further comprising a diluent.   The curable composition according to claim 1, further comprising a metal hydroxide.   The curable composition according to claim 15, wherein the metal hydroxide is aluminum hydroxide.