JP2006137797A - Autohesive organopolysiloxane composition - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide an autohesive organopolysiloxane composition giving a cured product capable of adhering well to a substrate such as a metal, a plastic, etc., particularly to a plastic. <P>SOLUTION: This autohesive organopolysiloxane composition comprises (A) 100 pts.mass of an organopolysiloxane containing at least two alkenyl groups each bonding to a silicon atom, (B) an organopolysiloxane containing at least two hydrogen atoms each bonding to a silicon atom in an amount of 0.5-10.0 mol hydrogen atom bonded to the silicon atom in the component(B) per 1 mol alkenyl group in the total composition, (C) an effective amount of catalyst for hydrosilylation reaction and (D) 0.01-10 pts.mass of isocyanuric ester having an epoxy group. <P>COPYRIGHT: (C)2006,JPO&NCIPI

Description

  The present invention relates to a self-adhesive organopolysiloxane composition that can be cured at a relatively low temperature and can form a cured product that adheres firmly to a substrate such as metal or plastic, particularly plastic, without using a primer. .

  Presence of a platinum-based catalyst comprising an addition-curable organopolysiloxane composition containing an organopolysiloxane containing an alkenyl group bonded to a silicon atom and an organohydrogensiloxane containing a hydrogen atom bonded to a silicon atom (SiH group) It is well known that an elastic cured product can be obtained by addition reaction under the above, and various compositions have been proposed.

  However, since the cured products obtained from these compositions are all poor in adhesion to metals, resins, etc., this is used for potting or coating electric circuits, impregnating motor coils, impregnating flyback transformers for TV sets, Disadvantages such as peeling of the semiconductor chip to the circuit board, bonding of the bonding part of the structure, or impregnation or coating of a film-like or woven-like resin, and the required characteristics cannot be obtained. There was a point.

  Therefore, in order to obtain an addition-curable organopolysiloxane composition having good adhesion to various substrates, studies have been made conventionally. For example, Patent Document 1 discloses a vinyl group-containing diorganopolysiloxane, 100 to 1 part by weight of an organohydrogenpolysiloxane having an epoxy group and / or an ester group, and an organohydrogenpolysiloxane having no epoxy group or ester group. Addition-curable compositions containing 0 to 99 parts by weight are described. Patent Document 2 describes an addition-curable organopolysiloxane composition containing an organopolysiloxane having a trialkoxysilyl group, an oxirane group, and a hydrosilyl group in one molecule.

  However, the adhesion performance of these conventional addition-curing organopolysiloxane compositions is not sufficient compared to other resin-based adhesives such as epoxy-based adhesives, and adhesion to substrates such as metals and plastics, especially plastics. There is a problem that the holding ability is inferior, and further improvement of the adhesion performance has been desired.

Japanese Patent Publication No.53-13508 Japanese Patent Publication No.59-5219

  In view of the above-mentioned problems, the present invention provides a self-adhesive material that provides a cured product that can adhere well to substrates such as metals, plastics, etc., which have poor adhesion with conventional addition-curable organopolysiloxane compositions. It is an object of the present invention to provide a functional organopolysiloxane composition.

The present inventors have made various studies to solve the above problems, and by adding an isocyanuric acid ester compound having an epoxy group to the addition-curable organopolysiloxane composition, the self-adhesion performance has been dramatically improved. I found out. That is, the present invention
(A) 100 parts by mass of an organopolysiloxane containing at least two alkenyl groups bonded to silicon atoms,
(B) Organohydrogenpolysiloxane containing at least two hydrogen atoms bonded to silicon atoms The amount of hydrogen atoms bonded to silicon atoms in this component (B) is 0.5 per mole of alkenyl groups in the total composition. Amount to be ~ 10.0 mol,
A self-adhesive organopolysiloxane composition comprising (C) an effective amount of a catalyst for hydrosilylation reaction, and (D) 0.01 to 10 parts by mass of an isocyanuric acid ester having an epoxy group is provided.

  The addition-curing self-adhesive organopolysiloxane composition according to the present invention is cured at a relatively low temperature, and a cured product that adheres firmly to a substrate such as metal or plastic, particularly plastic, without using a primer. There is an excellent effect that it can be formed. Therefore, the composition is useful as a sealing material, a potting material, a coating material, etc., for example, as a coating material or sealing material for resin fiber textile fabrics or general resin films used for air bags and the like.

  Hereinafter, the present invention will be described in detail.

[(A) component]
The organopolysiloxane of component (A) is a base polymer of the composition of the present invention, and contains at least two alkenyl groups bonded to silicon atoms in one molecule.

  Examples of the molecular structure of the component (A) include a linear structure and a cyclic structure, and these structures may have a branch, but the main chain basically consists of repeating diorganosiloxane units. Thus, a linear diorganopolysiloxane in which both ends of the molecular chain are blocked with a triorganosiloxy group is preferably used as the component (A).

  The viscosity of component (A) at 25 ° C. is preferably in the range of 100 to 500,000 mPa · s, and particularly preferably in the range of 500 to 100,000 mPa · s. When the viscosity is within this range, the handling workability of the composition and the physical strength of the silicone rubber obtained from the composition can be sufficiently ensured.

  As the alkenyl group bonded to the silicon atom in the component (A), for example, the number of carbon atoms such as vinyl group, allyl group, butenyl group, pentenyl group, hexenyl group, heptenyl group is preferably 2-8, more preferably. 2 to 4 may be mentioned, and a vinyl group is particularly preferable. In the case where the organopolysiloxane of component (A) has a linear structure, the alkenyl group is bonded to a silicon atom only in one of the molecular chain terminal and the non-molecular chain terminal. It may be bonded to an atom.

  (A) As an organic group couple | bonded with silicon atoms other than the alkenyl group in a component, for example, an alkyl group, especially a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, a hexyl group, a cyclohexyl group, a heptyl group Alkyl groups having 1 to 10 carbon atoms such as aryl groups, particularly phenyl groups, tolyl groups, xylyl groups, naphthyl groups and the like aryl groups having 6 to 14 carbon atoms; aralkyl groups, particularly benzyl groups and phenethyl groups Aralkyl groups having 7 to 14 carbon atoms such as halogenated alkyl groups, particularly halogenated alkyl groups having 1 to 3 carbon atoms such as chloromethyl group, 3-chloropropyl group, 3,3,3-trifluoropropyl group, etc. Examples thereof include an unsubstituted or halogen-substituted monovalent hydrocarbon group such as an alkyl group, and a methyl group and a phenyl group are particularly preferable.

Specific examples of the component (A) include: a trimethylsiloxy group-capped dimethylsiloxane / methylvinylsiloxane copolymer at both ends of a molecular chain, a trimethylsiloxy group-capped methylvinylpolysiloxane at both ends of a molecular chain, and a trimethylsiloxy group-capped dimethyl at both molecular chains. Siloxane / methylvinylsiloxane / methylphenylsiloxane copolymer, dimethylpolysiloxane blocked with dimethylvinylsiloxy group at both ends of molecular chain, dimethylvinylsiloxy group-blocked methylvinylpolysiloxane with molecular chain at both ends, dimethylvinylsiloxy group-blocked dimethyl with molecular chain at both ends Siloxane / methylvinylsiloxane copolymer, dimethylvinylsiloxy group with both ends of molecular chain blocked dimethylsiloxane / methylvinylsiloxane / methylphenylsiloxane copolymer, trivinylsiloxy group with both ends of molecular chain Blocked dimethylpolysiloxane, siloxane unit represented by the formula: R ¹ ₃ SiO _0.5 (R ¹ is an unsubstituted or substituted monovalent hydrocarbon group other than an alkenyl group, the same shall apply hereinafter) and the formula: R ¹ ₂ R ² Organopolysiloxane copolymer comprising a siloxane unit represented by SiO _0.5 (R ² is an alkenyl group; the same shall apply hereinafter), a unit represented by the formula: R ¹ ₂ SiO and a siloxane unit represented by the formula: SiO ₂ An organopolysiloxane copolymer comprising a siloxane unit represented by the formula: R ¹ ₃ SiO _0.5 , a siloxane unit represented by the formula: R ¹ ₂ R ² SiO _0.5 and a siloxane unit represented by the formula: SiO ₂ , An organopolysiloxane copolymer comprising a siloxane unit represented by R ¹ ₂ R ² SiO _0.5 and a siloxane unit represented by the formula: R ¹ ₂ SiO and a siloxane unit represented by the formula: SiO ₂ , a formula: R ¹ R ² Examples thereof include an organopolysiloxane copolymer comprising a siloxane unit represented by SiO and a siloxane unit represented by the formula: R ¹ SiO _1.5 or a siloxane unit represented by the formula: R ² SiO _1.5 . These can be used singly or in combination of two or more.

R ¹ in the above formula is, for example, an alkyl group such as a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, a hexyl group, or a heptyl group; an aryl group such as a phenyl group, a tolyl group, a xylyl group, or a naphthyl group. Groups: aralkyl groups such as benzyl group and phenethyl group; halogenated alkyl groups such as chloromethyl group, 3-chloropropyl group and 3,3,3-trifluoropropyl group. Examples of R ² in the above formula include a vinyl group, an allyl group, a butenyl group, a pentenyl group, a hexenyl group, and a heptenyl group.

[(B) component]
The (B) component organohydrogenpolysiloxane reacts with the (A) component and acts as a crosslinking agent. (B) There is no restriction | limiting in particular in the molecular structure of a component, For example, using various organohydrogen polysiloxane manufactured conventionally, such as linear, cyclic, branched, and three-dimensional network structure (resin form) Can do.

  (B) Component organohydrogenpolysiloxane is 2 or more, preferably 3 or more (usually 3 to 500, preferably 3 to 200, more preferably about 3 to 100) in one molecule. It has a hydrogen atom (ie, hydrosilyl group or SiH group) bonded to a silicon atom. When the organohydrogenpolysiloxane of component (B) has a linear structure, these SiH groups are located in both of the molecular chain terminal and the non-molecular chain terminal part, even if they are located only in either one. It may be.

  The number (degree of polymerization) of silicon atoms in one molecule of component (B) is preferably 2 to 1,000, more preferably 3 to 300, and still more preferably about 4 to 150. Furthermore, the viscosity of the component (B) at 25 ° C. is preferably 0.1 to 5,000 mPa · s, more preferably 0.5 to 1,000 mPa · s, and still more preferably about 5 to 500 mPa · s.

As the component (B), for example, the following average composition formula (1):
R ³ _a H _b SiO _{(4-ab) / 2} (1)
(In the formula, R ³ is an unsubstituted or substituted monovalent hydrocarbon group having 1 to 14 carbon atoms, more preferably 1 to 10 carbon atoms bonded to a silicon atom, excluding an aliphatic unsaturated group. A and b are preferably 0.7 ≦ a ≦ 2.1, 0.001 ≦ b ≦ 1.0, and 0.8 ≦ a + b ≦ 3.0, more preferably 0.9 ≦ a ≦ 2.0, 0.01 ≦ b ≦ 1.0, and 1.0 ≦ a + b ≦ It is a positive number that satisfies 2.5)
The organohydrogenpolysiloxane shown by these is used.

Examples of R ³ include a methyl group, ethyl group, propyl group, isopropyl group, butyl group, isobutyl group, tert-butyl group, pentyl group, neopentyl group, hexyl group, cyclohexyl group, octyl group, nonyl group, Alkyl group such as decyl group; aryl group such as phenyl group, tolyl group, xylyl group and naphthyl group; aralkyl group such as benzyl group, phenylethyl group and phenylpropyl group; a part of hydrogen atoms in these hydrocarbon groups or Groups substituted entirely with halogen atoms such as fluorine, bromine and chlorine, such as chloromethyl group, 3-chloropropyl group, bromoethyl group, 3,3,3-trifluoropropyl group, etc., preferably alkyl group An aryl group, more preferably a methyl group or a phenyl group.

  Component (B) can be obtained by a known production method. General production methods such as 1,3,5,7-tetramethyl-1,3,5,7-tetrahydrocyclotetrasiloxane (in some cases a mixture of the cyclotetrasiloxane and octamethylcyclotetrasiloxane) ) And hexamethyldisiloxane, 1,3-dihydro-1,1,3,3-tetramethyldisiloxane, or other siloxane compounds that serve as end group sources, or octamethylcyclotetrasiloxane and 1,3-dihydro By equilibrating -1,1,3,3-tetramethyldisiloxane in the presence of a catalyst such as sulfuric acid, trifluoromethanesulfonic acid, methanesulfonic acid, etc. at a temperature of about −10 to + 40 ° C. Component (B) can be obtained.

Specific examples of component (B) include 1,1,3,3-tetramethyldisiloxane, 1,3,5,7-tetramethylcyclotetrasiloxane, tris (dimethylhydrogensiloxy) methylsilane, tris (dimethylhydro Jensiloxy) phenylsilane, trimethylsiloxy group-capped methylhydrogen polysiloxane with molecular chain at both ends, trimethylsiloxy group-capped dimethylsiloxane / methylhydrogensiloxane copolymer with molecular chain at both ends, trimethylsiloxy group-capped dimethylsiloxane with molecular chain at both ends Methylhydrogensiloxane / methylphenylsiloxane copolymer, dimethylhydrogensiloxy group-blocked dimethylpolysiloxane at both molecular chains, dimethylhydrogensiloxy group-blocked dimethylpolysiloxane / methylhydrogenl at both molecular chains Hexane copolymer, both molecular terminals with dimethylhydrogensiloxy groups dimethylsiloxane-methylphenylsiloxane copolymers, dimethylpolysiloxane with both molecular chain terminals hydro diene siloxy groups at methylphenyl polysiloxane, ^{_{formula: R 1 3 SiO 0.5 (R}} 1 Is as defined and exemplified for the component (A), the same shall apply hereinafter)), an organo comprising a siloxane unit represented by the formula: R ¹ ₂ HSiO _0.5 and a siloxane unit represented by the formula: SiO _2. Polysiloxane copolymer, organopolysiloxane copolymer comprising a siloxane unit represented by the formula: R ¹ ₂ HSiO _0.5 and a siloxane unit represented by the formula: SiO ₂ , a siloxane unit represented by the formula: R ¹ HSiO : siloxane units or of the formula represented by R ¹ SiO _1.5: siloxane units represented by HSiO _1.5 Ranaru organopolysiloxane copolymer. These can be used singly or in combination of two or more.

  The blending amount of the component (B) is bonded to the silicon atom in the component (A), particularly per mole of the alkenyl group bonded to the silicon atom in the entire composition. The amount of hydrogen atoms (SiH groups) bonded to silicon atoms in the component (B) per mole of alkenyl groups is in the range of 0.5 to 10.0 moles, preferably 1.0 to 8.0 moles. At this time, the ratio of the alkenyl group bonded to the silicon atom in the component (A) to the alkenyl group present in the entire composition is preferably 50 to 100 mol%, more preferably 80 to 100 mol%. When only component (A) is present as a component having an alkenyl group in the whole composition, the amount of SiH groups in component (B) per mole of alkenyl groups bonded to silicon atoms in component (A) Is in the range of 0.5 to 10.0 mol, preferably 1.0 to 8.0 mol. If the blending amount of the component (B) is too small, the composition may not be cured sufficiently. Conversely, if the amount is too large, the heat resistance of the resulting silicone rubber may be extremely poor.

[(C) component]
As the catalyst for hydrosilylation reaction of component (C), any catalyst may be used as long as it promotes the addition reaction between the alkenyl group in component (A) and the SiH group in component (B). . For example, platinum catalysts such as chloroplatinic acid, alcohol-modified chloroplatinic acid, coordination compounds of chloroplatinic acid and olefins, vinyl siloxane or acetylene compounds; palladium catalysts such as tetrakis (triphenylphosphine) palladium; chlorotris ( A rhodium catalyst such as triphenylphosphine) rhodium is used as the component (C), and a platinum catalyst is particularly preferable.

  The compounding amount of component (C) is not particularly limited as long as it is an effective amount as a catalyst for hydrosilylation reaction, but based on the total amount of components (A) and (B), converted into a catalytic metal element based on mass And preferably in the range of 0.1 to 1,000 ppm, more preferably 1 to 500 ppm, even more preferably 10 to 100 ppm. When the addition amount is within this range, the addition reaction is sufficiently accelerated, the curing is sufficient, and this is economically advantageous.

[(D) component]
(D) component is an isocyanuric acid ester which has an epoxy group, and provides self-adhesiveness to this invention composition. As the component (D), for example, the following general formula (1):

（１）

（式中、R⁴は独立にエポキシ基含有基を表し、R⁵は独立に水素原子、またはエポキシ基を含有しない基を表し、xは1〜3の整数を表し、yは0〜2の整数を表し、ただし、x+yは３である。）
で表されるイソシアヌレート化合物が挙げられる。

(1)

(In the formula, R ⁴ independently represents an epoxy group-containing group, R ⁵ independently represents a hydrogen atom or a group not containing an epoxy group, x represents an integer of 1 to 3, and y represents 0 to 2 Represents an integer, where x + y is 3.)
The isocyanurate compound represented by these is mentioned.

Examples of the epoxy group-containing group represented by R ⁴ include:

（式中、R⁶は炭素原子数１〜１０、好ましくは炭素原子数１〜６の直鎖状もしくは分岐状のアルキレン基を表す。）、

(Wherein R ⁶ represents a linear or branched alkylene group having 1 to 10 carbon atoms, preferably 1 to ⁶ carbon atoms),

（式中、R⁶は前記と同様であり、R⁷は炭素原子数１〜１０、好ましくは炭素原子数１〜６の直鎖状もしくは分岐状のアルキレン基を表す。）、

(Wherein R ⁶ is as defined above, and R ⁷ represents a linear or branched alkylene group having 1 to 10 carbon atoms, preferably 1 to 6 carbon atoms),

（式中、R⁶は前記と同様である。）
が挙げられ、その具体例としては、

(Wherein R ⁶ is the same as described above.)
As a specific example,

（式中、ｍは１〜３の整数である。）、

(Wherein m is an integer of 1 to 3),

（式中、ｍおよびｎは独立に１〜３の整数である。）、

(Wherein, m and n are each independently an integer of 1 to 3),

（式中、ｍは１〜３の整数である。）
などが挙げられる。

(In the formula, m is an integer of 1 to 3.)
Etc.

Examples of R ⁵ include a hydrogen atom; an alkyl group such as a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, an isobutyl group, and a tert-butyl group; a vinyl group, an allyl group, a propenyl group, and a butenyl group. An alkenyl group of (meth) acryloxyalkyl group such as γ-acryloxypropyl group and γ-methacryloxypropyl group; formula: (R ⁸ O) ₃ Si—R ⁷ — or formula: (R ⁸ O) ₃ Si -R ⁶ -OR ⁷ - (wherein, R ⁶ and R ⁷ are the same as defined above, R ⁸ is a methyl group, an ethyl group, a propyl group, an isopropyl group, butyl group, isobutyl group, tert- butyl group, a hexyl And a partially hydrolyzed condensate thereof, for example, a compound represented by the formula: (CH 2 represents an alkyl group having 1 to 6 carbon atoms, preferably 1 to 4 carbon atoms such as a cyclohexyl group) _{3 O) 3 Si- (CH 2} ) m - Moshiku _{Formula: - (C 2 H 5 O} ) 3 Si- (CH 2) m group represented by (. Wherein, m is an integer from 2 to 4); silyl derivatives with or SiH groups, for example, the formula: (R ⁸ O) ₂ (H) Si—R ⁹ — or the formula: (R ⁸ O) ₂ (H) Si—R ⁹ —OR ¹⁰ — (wherein R ⁸ is as defined above, R ⁹ and R ¹⁰ independently represents a group having 1 to 10 carbon atoms which may contain a nitrogen atom, preferably a linear or branched alkylene group having 1 to 6 carbon atoms. It is done.

  Specific examples of the component (D) include the following compounds.

1,3,5-triglycidyl isocyanuric acid:

（以下、「接着性付与剤(a)」という）

(Hereinafter referred to as “adhesiveness imparting agent (a)”)

1-allyl-3,5-diglycidyl isocyanuric acid:

（以下、「接着性付与剤(b)」という）

(Hereinafter referred to as “adhesion imparting agent (b)”)

1,3-diallyl-5-glycidyl isocyanuric acid:

（以下、「接着性付与剤(c)」という）

(Hereinafter referred to as “adhesion imparting agent (c)”)

  (D) The compounding quantity of a component should just be sufficient quantity to provide favorable adhesiveness to this invention composition, and is 0.01-10 mass parts normally with respect to 100 mass parts of (A) component, Preferably it is the range of 0.05-5 mass parts. If the blending amount is too small, good adhesiveness may not be imparted to the composition of the present invention. If the blending amount is too large, a cured silicone product having the desired rubber strength may not be obtained. is there.

  There is no restriction | limiting in particular as a compounding method of (D) component. For example, the component (D) may be added and dispersed in the silicone composition as it is. Further, the component (D) may be added to and dispersed in the silicone composition after being dissolved in a suitable solvent. Further, when the component (D) is solid at room temperature because the melting point of the component (D) is not less than room temperature (for example, 23 ° C.), the component (D) is added to an appropriate dispersion (for example, organo After mixing with siloxane or the like, a paste-like mixture obtained by uniformly dispersing using a device such as a three-roll mill may be added to and dispersed in the silicone composition.

[Other ingredients]
In this composition, in addition to the above-mentioned components (A) to (D), as an optional component, all conventionally known inclusions for controlling agents that are said to have a curing inhibiting effect on the addition reaction catalyst are used. can do. Examples of such compounds include phosphorus-containing compounds such as triphenylphosphine, nitrogen-containing compounds such as tributylamine and tetramethylethylenediamine and benzotriazole, sulfur-containing compounds, and acetylene-based compounds such as 1-ethynyl-1-hexanol, Examples include triallyl isocyanuric acid, hydroperoxy compounds, and maleic acid derivatives. The degree of the retarding effect by the control agent compound varies greatly depending on the chemical structure of the control agent compound. Therefore, the addition amount of the control agent compound should be adjusted to an optimum amount for each of the control agent compounds to be used, but such adjustment can be easily performed by methods well known to those skilled in the art. In general, if the amount added is too small, the long-term storage stability of the composition of the present invention cannot be obtained at room temperature. Conversely, if the amount added is too large, curing of the composition is inhibited.

As other optional components, for example, fumed silica, crystalline silica, precipitated silica, hollow filler, silsesquioxane, fumed titanium dioxide, magnesium oxide, zinc oxide, iron oxide, aluminum hydroxide, magnesium carbonate , Calcium carbonate, zinc carbonate, layered mica, carbon black, diatomaceous earth, glass fiber, and other inorganic fillers, and these fillers as organoalkoxysilane compounds, organochlorosilane compounds, organosilazane compounds, low molecular weight siloxane compounds, etc. And a filler treated with an organosilicon compound. Examples of the filler include silicone rubber powder and silicone resin powder.

  Furthermore, in the composition of the present invention, as long as the object of the present invention is not impaired, as other optional components, for example, an organopolysiloxane containing one hydrogen atom or alkenyl group bonded to a silicon atom in one molecule, Organopolysiloxane containing neither hydrogen atom nor alkenyl group bonded to silicon atom, organic solvent, creep hardening inhibitor, heat resistance imparting agent, flame retardant imparting agent, plasticizer, thixotropy imparting agent, pigment, dye In addition, an antifungal agent or the like may be contained.

[Use of composition]
The self-adhesive organopolysiloxane composition of the present invention is cured at a relatively low temperature, and can form a cured product that adheres firmly to a substrate such as metal or plastic without using a primer. Therefore, the composition can be used as a sealing material, a potting material, a coating material, etc., for example, as a coating material or sealing material for a resin fiber textile fabric or a general resin film used for an air bag or the like.

  In use, the composition of the present invention can be cured by heating after being applied to a predetermined substrate depending on the application. The curing conditions of the composition of the present invention vary depending on the amount and are not particularly limited. The curing temperature is preferably 60 to 200 ° C, more preferably 100 to 180 ° C. Usually, it hardens in about 0.5 to 10 minutes.

  EXAMPLES Hereinafter, although an Example and a comparative example are shown and this invention is demonstrated more concretely, this invention is not limited to these Examples. In the following examples, “part” means “part by mass”. The viscosity is a measured value at 25 ° C.

Example 1
(A) 100 parts of dimethylpolysiloxane with a viscosity of 10 Pa · s, both ends of the molecular chain blocked with dimethylvinylsiloxy groups, (B) Trimethylsiloxy group-capped methylhydrogen with a viscosity of 5 mPa · s Polysiloxane (content of SiH group = 1.45% by mass) 2.0 parts (SiH group in component (B) / vinyl group in component (A) (molar ratio) = 5.3), (C) chloroplatinic acid and divinyltetra Methyldisiloxane complex 30 ppm by mass based on the total amount of components (A) and (B), (D) Adhesive agent (a) 0.3 parts, 3,5- Composition of 0.15 parts of dimethyl-1-hexyn-3-ol (added as a retarder) and 15 parts of silica with a specific surface area of 120 m ² / g treated with hexamethyldisilazane (added as hydrophobic silica) Product A was prepared. In addition, when the above component (D) is actually added, the adhesion-imparting agent (a), dimethylpolysiloxane having a viscosity of 100 Pa · s, both ends of which are blocked with dimethylvinylsiloxy groups, and After equal mass mixing, 0.6 parts of a paste mixture prepared by uniformly dispersing in a three-roll mill was dispersed in the composition.

Example 2
A composition B was prepared in the same manner as in Example 1, except that the adhesion-imparting agent (a) of the component (D) was replaced with the adhesion-imparting agent (b) in Example 1.

Example 3
In Example 1, when the adhesion-imparting agent (a) of the component (D) is replaced with the adhesion-imparting agent (c), and the component (D) is actually added, the adhesion-imparting agent (c) A composition C was prepared in the same manner as in Example 1 except that 0.6 part of a methanol solution prepared by uniformly dissolving the lysate in an equal mass of methanol was dispersed in the composition.

Comparative Example 1
In Example 1, the compound (i) represented by the following structural formula is used as the adhesion imparting agent (a) as the component (D):

に置き換えた以外は、実施例1と同様にして組成物Ｄを調製した。

Composition D was prepared in the same manner as in Example 1 except that

Comparative Example 2
In Example 1, Composition E was prepared in the same manner as in Example 1, except that the adhesion-imparting agent (a) of component (D) was replaced with γ-glycidoxypropyltrimethoxysilane.

Shear adhesion test These compositions A, B, C, D, and E were poured into an aluminum plate, a Nylon 66 plate, and an SPS (syndiotactic polystyrene) plate so as to have a thickness of 2 mm. It was cured by heating at 1 ° C. for 1 hour. After returning to room temperature, a shear adhesive strength test was conducted using a shopper type tensile tester under a tensile speed of 50 mm / min in accordance with the tensile shear bond strength test method of the adhesive specified in JIS K 6850. The cohesive failure rate was measured by visually observing the fracture state of the sample subjected to the shear adhesion test. The results are shown in Table 1.

As shown in Evaluation Table 1, the cured products of the examples showed higher shear adhesion and cohesive failure rate than the cured products of the comparative examples for any adherend. This shows that the composition of an Example can form the hardened | cured material which adhere | attaches firmly on a metal base material and a plastic base material, without using a primer.

Example 4
(A) 60 parts of dimethylpolysiloxane with both ends of the molecular chain blocked with dimethylvinylsiloxy groups and having a viscosity of about 30 Pa · s. Similarly, both ends of the molecular chain were blocked with dimethylvinylsiloxy groups and the viscosity was about 5 Pa. 20 parts of dimethylpolysiloxane which is s, and 20 parts of vinyl group-containing methylpolysiloxane resin (vinyl group content: 2.3% by mass) composed of Vi (Me) ₂ SiO _1/2 units and SiO _4/2 units, (B) Molecular chain both ends trimethylsiloxy group-capped methylhydrogenpolysiloxane with a viscosity of 5 mPa · s (SiH group content = 1.45% by mass) 3.1 parts (SiH group in component (B) / component (A)) Vinyl group (molar ratio) = 2.3), (C) complex of chloroplatinic acid and divinyltetramethyldisiloxane (A) and the total amount of component (B), based on mass in terms of platinum metal element 30 ppm, (D) Adhesive agent (b) 0.3 part, 3,5 -Prepare composition F by uniformly mixing 0.10 parts of dimethyl-1-hexyn-3-ol (added as a retarder) and 0.5 parts of Bengala (added so that the coating state can be visually confirmed). did. When the component (D) is actually added, the adhesion-imparting agent (b), dimethylpolysiloxane having a viscosity of 100 Pa · s with both ends of the molecular chain blocked with dimethylvinylsiloxy groups, and After equal mass mixing, 0.6 parts of a paste mixture prepared by uniformly dispersing in a three-roll mill was dispersed in the composition.

Comparative Example 3
In Example 4, the adhesion-imparting agent (b) as the component (D) is a compound (ii) represented by the following structural formula:

に置き換えた以外は、実施例４と同様にして組成物Ｇを調製した。

Composition G was prepared in the same manner as in Example 4 except that

Comparative Example 4
In Example 4, the compound (iii) represented by the following structural formula is used as the adhesion-imparting agent (b) of the component (D):

に置き換えた以外は、実施例４と同様にして組成物Ｈを調製した。

A composition H was prepared in the same manner as in Example 4 except that

Smoldering durability evaluation These compositions F, G, and H were uniformly coated on a Nylon 66 fiber woven fabric (420 denier) with a knife coater so that the average coating amount was about 30 g / m ^2, and 170 ° C. in an oven. And cured by heating for 1 minute. Next, the coated textile fabric was cut into a strip shape having a width of 30 mm and a length of 150 mm, and the coated surfaces were bonded together to prepare a test piece. This test piece was subjected to a Scott type stagnation tester to evaluate stagnation durability of the coated surface. Specifically, the evaluation should be carried out by visually observing the peeled state of the silicone rubber on the coated surface from the surface of the textile fabric after performing a sag test 500 times, 1000 times and 1500 times at a pressing pressure of 1 kgf / cm ^2. It went by. The results are shown in Table 2.

As shown in Evaluation Table 2, the cured products of the examples exhibited higher durability against stagnation than the cured products of the comparative examples. This shows that the composition of an Example can form the hardened | cured material which adhere | attaches firmly also on resin fiber textile fabric.

Claims (3)

(A) 100 parts by mass of an organopolysiloxane containing at least two alkenyl groups bonded to silicon atoms,
(B) Organohydrogenpolysiloxane containing at least two hydrogen atoms bonded to silicon atoms The amount of hydrogen atoms bonded to silicon atoms in this component (B) is 0.5 per mole of alkenyl groups in the total composition. Amount to be ~ 10.0 mol,
A self-adhesive organopolysiloxane composition comprising (C) an effective amount of a catalyst for hydrosilylation reaction, and (D) 0.01 to 10 parts by mass of an isocyanuric acid ester having an epoxy group.   The self-adhesive organopolysiloxane composition according to claim 1, wherein the component (D) has an alkenyl group. The self-adhesive organopolysiloxane composition according to claim 1 or 2, wherein component (D) has a melting point of 23 ° C or higher.