JP2010280813A - Method for forming reactive solid surface - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a method for forming a solid surface exhibiting excellent reactivity with a solid material such as a rubber, a resin, a metal, a ceramic and the like. <P>SOLUTION: The method for forming a reactive solid surface comprises using a triazinethiol derivative and is applicable to a solid material having a resin layer containing no hydroxy groups. The method comprises a step for causing a compound represented by general formula (1) to adhere on the surface of a solid having a resin layer at least on the surface thereof and a subsequent step for causing a compound represented by general formula (2) to adhere on the surface of the solid. <P>COPYRIGHT: (C)2011,JPO&INPIT

Description

  The present invention relates to a method for forming a reactive solid surface excellent in reactivity with solid materials such as rubber, resin, metal and ceramics.

  Conventionally, a method using an adhesive has been widely used as a method for bonding different kinds of materials. In particular, there are many needs for bonding rubber to solid materials such as resin, metal and ceramics, such as rubber products for electrical and electronic parts, rubber products for construction, automobile parts, etc., but in terms of cost and reliability The current situation is that there is no satisfactory bonding method. For example, when rubber is bonded to the resin, after pre-treatment such as degreasing or blasting on the resin surface, primer coating and adhesive coating are performed, and the unvulcanized rubber is brought into contact with the pressure-bonding method. It has been known. However, since this method requires a complicated process, there is a problem that the cost of the product increases. In addition, it is necessary to select an adhesive according to the type of the solid material and the adhesive, and there is a problem that it takes time for the selection. Therefore, there is a need for an adhesion method that is simpler and that can be performed at a lower cost.

  On the other hand, one of the inventors of the present invention has proposed an adhesion method using a triazine thiol derivative as an adhesion method between a rubber and a different material (Patent Document 1). This method is intended for a solid material having a resin layer on at least a surface, and the resin layer has a hydroxyl group. Here, the phrase “the resin layer has a hydroxyl group” means a case where a hydroxyl group is contained in a monomer unit of the resin and a case where a hydroxyl group is introduced into the resin surface by surface treatment. According to this method, the rubber can be firmly adhered to the solid material simply by attaching the triazine thiol derivative to the surface of the solid material and then thermally bonding the rubber to the surface of the solid material. Here, this triazine thiol derivative has an alkoxysilyl group as a functional group capable of reacting with a hydroxyl group on the surface of the solid material. Since this triazine thiol derivative also has a functional group (thiol group) that reacts with rubber, it can be chemically bonded to rubber by thermocompression bonding of the rubber. That is, this triazine thiol derivative has both a functional group capable of reacting with a hydroxyl group on the surface of a solid material and a functional group chemically bonded to rubber, and can bond a different material at a molecular level. This adhesion method changes the surface of a solid material to a reactive solid surface having high reactivity with rubber by attaching a triazine thiol derivative, and is also a method for forming a reactive solid surface.

JP 2007-119752 A

  The method for forming a reactive solid surface using the above-mentioned triazine thiol derivative can be performed in a simpler process as compared with the conventional method because a solid material having a resin layer on the surface does not require pretreatment of the solid material. And rubber can be firmly bonded. However, the application target is limited to a resin layer having a hydroxyl group, and there is a problem that it cannot be applied to a resin layer having no hydroxyl group. Introducing a hydroxyl group into the resin layer can be performed by surface treatment such as corona discharge treatment, atmospheric pressure plasma treatment, chemical treatment, etc., but this complicates the process and makes it difficult to reduce costs.

  Accordingly, the present inventor provides a method for forming a reactive solid surface using a triazine thiol derivative, which is applicable to a solid material having a resin layer not having a hydroxyl group. Aimed at that.

  In order to solve the above problems, the method for forming a reactive solid surface of the present invention comprises a step of attaching a compound represented by the general formula (1) to the surface of a solid material having a resin layer on at least the surface; And a step of attaching the compound represented by the general formula (2) to the surface of the solid.

Here, R1 is a monovalent aliphatic hydrocarbon group having 1 to 20 carbon atoms which may have a substituent, a monovalent aromatic hydrocarbon group which may have a substituent, or hydrogen. Represents an atom. R2 represents a C1-C20 divalent aliphatic hydrocarbon group which may have a substituent, a divalent aromatic hydrocarbon group which may have a substituent, or a carbonyl group. The aliphatic hydrocarbon group may contain a hetero atom or a functional group. X ¹ is a monovalent aliphatic hydrocarbon group having 1 to 20 carbon atoms which may have a substituent, a monovalent aromatic hydrocarbon group which may have a substituent, a halogen atom or hydrogen. Represents an atom. Y ¹ represents an alkoxy group having 1 to 10 carbon atoms. n is a natural number of 1 to 3.

Here, R3 represents a monovalent aliphatic hydrocarbon group having 1 to 4 carbon atoms which may have a substituent, a monovalent aromatic hydrocarbon group which may have a substituent, or a hydrogen atom. To express. R4 represents a C1-C20 divalent aliphatic hydrocarbon group which may have a substituent, and the aliphatic hydrocarbon group may include a hetero atom or a functional group. X ² represents a monovalent aliphatic hydrocarbon group having 1 to 20 carbon atoms which may have a substituent. Y ² represents an alkoxy group having 1 to 10 carbon atoms. n represents a natural number of 1 to 3. M represents a hydrogen atom or an alkali metal.

  The resin preferably has a carbonyl group in at least one constituent monomer unit.

  In the compound represented by the general formula (1), R1 is preferably a hydrogen atom.

  In the compound represented by the general formula (1), R2 is preferably a C1-C20 divalent aliphatic hydrocarbon group which may have a substituent.

  In the present invention, an amino group-containing alkoxysilane compound represented by the general formula (1) is adhered to at least the surface of a solid material having a resin layer on the surface, and then a triazine thiol derivative represented by the general formula (2) is adhered. Let Even if the said resin layer consists of resin which does not contain a hydroxyl group, the amino group containing alkoxysilane compound shown by General formula (1) can be couple | bonded with the resin layer. The triazine thiol derivative and the amino group-containing alkoxysilane compound are bonded to each other by a condensation reaction. As a result, the triazine thiol derivative is fixed to the surface resin layer of the solid material via the amino group-containing alkoxysilane compound. Since the triazine thiol derivative has a thiol group as a reactive group, it can react with another material. Thereby, it becomes possible to adhere | attach various solid materials using a triazine thiol derivative, without being restrict | limited to the kind of resin layer. Of course, since it is not necessary to perform a corona discharge treatment, an atmospheric pressure plasma treatment, a chemical treatment or the like in order to introduce a hydroxyl group into the resin layer as in the prior art, adhesion can be performed at a lower cost.

  The method for forming a reactive solid surface of the present invention comprises a step of attaching an amino group-containing alkoxysilane compound represented by the general formula (1) to at least the surface of a solid material having a resin layer on the surface, and then the solid material. Attaching a triazine thiol derivative represented by the general formula (2) to the surface of

  The reactive solid surface of the present invention is a solid surface in which a solid material made of rubber, resin, metal or ceramics is used as a base material, and a resin layer is formed on the surface of the base material. This means that the sex group is fixed. The reactive group means a group capable of reacting with another solid material. When the solid material is a resin, the resin layer refers to a layer portion having a composition different from that of the solid material or a surface portion of the solid material itself. The shape of the solid material used in the present invention is not particularly limited as long as a resin layer can be formed on the surface, and can take a plate shape, a film shape, a powder shape, a fine particle shape, or the like. Further, the size and thickness of the solid material are not particularly limited.

  In the present invention, the amino group-containing alkoxysilane compound represented by the general formula (1) is attached to the resin layer on the surface of the solid material. Next, a triazine thiol derivative represented by the general formula (2) (hereinafter abbreviated as triazine thiol derivative) is attached to the surface of the solid material. The silyl group of the amino group-containing alkoxysilane compound undergoes a condensation reaction with the silyl group of the triazine thiol derivative, and the triazine thiol derivative is fixed to the resin layer on the surface of the solid material via the amino group-containing alkoxysilane compound. Since the triazine thiol derivative has a thiol group as a reactive group, the triazine thiol derivative can react with other solid materials.

  The resin used for the resin layer formed on the surface of the solid material is not particularly limited as long as it does not have a hydroxyl group in the constituent monomer unit. Specific examples include olefin resin, styrene resin, vinyl resin, chroman indene resin, terpene resin, (meth) acrylic resin, ethylene oxide resin, propylene oxide resin, polyester resin, polycarbonate resin, vinyl acetate resin, vinylidene fluoride resin, Thermoplastic resins such as vinyl chloride resin, ABS resin, polyacetal resin, polyamide resin, polyamideimide resin, polysulfone resin, polyphenylene ether resin, polyphenylene sulfide resin, polyether ether ketone resin, liquid crystal polymer, xylene resin, guanamine resin, diallyl Examples include thermosetting resins such as phthalate resins, vinyl ester resins, unsaturated polyester resins, furan resins, imide resins, urethane resins, maleic resins, and melamine resins. . Of course, these resins can also be used as a substrate of a reactive solid.

  The resin used for the resin layer formed on the surface of the solid material is preferably one having a carbonyl group in at least one constituent monomer unit. This is because the amino group-containing alkoxysilane compound is strongly fixed to the resin by hydrogen bonding with the amino group of the amino group-containing alkoxysilane compound. Examples of the resin having a carbonyl group include acrylic resin, polyester resin, polyamide resin, and urethane resin. Acrylic resin is preferable. More preferred is a photosensitive acrylic resin. This is because a resin layer having a desired pattern can be formed by performing development processing by using a photosensitive acrylic resin. Examples of the photosensitive acrylic resin include acrylamide and methacrylamide having a carbonyl group.

  In addition, this invention does not exclude using resin which has a hydroxyl group in a structural monomer unit as resin used for a resin layer at all. The present invention can also be applied to a resin having a hydroxyl group in a constituent monomer unit. Examples of the resin include cellulose and derivatives thereof, hydroxyethyl cellulose, starch, cellulose diacetate, surface saponified vinyl acetate resin, phenol-formalin resin, hydroquinone-formalin resin, cresol-formalin resin, polyvinylphenol resin, resorcin-formalin. Examples thereof include resins, cellophane, epoxy resins, modified epoxy resins, hydroxyl group-containing polyvinyl formal resins, hydroxyethyl (meth) acrylate homopolymers or copolymers thereof, polyvinyl alcohol or copolymers thereof.

  In the present invention, an amino group-containing alkoxysilane compound represented by the following general formula (1) is used.

Here, R1 is a monovalent aliphatic hydrocarbon group having 1 to 20 carbon atoms which may have a substituent, a monovalent aromatic hydrocarbon group which may have a substituent, or hydrogen. Represents an atom. R1 is preferably a hydrogen atom. This is because the amino group-containing alkoxysilane compound is easily arranged on the surface of the solid material. R2 represents a C1-C20 divalent aliphatic hydrocarbon group which may have a substituent, a divalent aromatic hydrocarbon group which may have a substituent, or a carbonyl group. The aliphatic hydrocarbon group may contain a hetero atom or a functional group. R2 is preferably an aliphatic hydrocarbon group. This is because the amino group-containing alkoxysilane compound is easily arranged on the surface of the solid material. X ¹ is a monovalent aliphatic hydrocarbon group having 1 to 20 carbon atoms which may have a substituent, a monovalent aromatic hydrocarbon group which may have a substituent, a halogen atom or hydrogen. Represents an atom. Y ¹ represents an alkoxy group having 1 to 10 carbon atoms. n is a natural number of 1 to 3.

  Here, as monovalent aliphatic hydrocarbon having 1 to 20 carbon atoms, methyl group, ethyl group, propyl group, isopropyl group, butyl group, isobutyl group, t-butyl group, amyl group, hexyl group, octyl group Decyl group, undecyl group, dodecyl group, tridecyl group, tetradecyl group, pentadecyl group, hexadecyl group, heptadecyl group, octadecyl group, nonadecyl group, eicosane group and the like. The monovalent aromatic hydrocarbon is preferably an aromatic hydrocarbon having 6 to 14 carbon atoms, and an aryl group such as a phenyl group, a naphthyl group, a toluyl group, a biphenyl group, a phenanthryl group, an anthranyl group, and a mesityl group. And aralkyl groups such as a benzyl group, a phenethyl group, a naphthylmethyl group, and a biphenylmethyl group. In addition, the divalent aliphatic hydrocarbon group having 1 to 20 carbon atoms may be linear, branched or cyclic, and is a methylene group, ethylene group, trimethylene group, tetramethylene group, hexamethylene group, nonamethylene. Group, decamethylene group, isopropylidene group and the like. Examples of the divalent aromatic hydrocarbon include phenylene group, biphenylene group, terphenylene group, naphthylene group, anthranylene group, phenanthrylene group, pyrenylene group, chrysenylene group, and fluoranthenylene group. Examples of the halogen atom include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom. Examples of the alkoxy group having 1 to 10 carbon atoms include methoxy group, ethoxy group, propoxy group, isopropoxy group, butoxy group, isobutoxy group, t-butoxy group, hexyloxy group, 2-ethylhexyloxy group, and decyloxy group. Can be mentioned.

  Moreover, as a substituent which said aliphatic hydrocarbon and aromatic hydrocarbon may have, a C1-C10 alkyl group and a C1-C10 alkoxy group can be mentioned. Here, the alkyl group having 1 to 10 carbon atoms includes methyl group, ethyl group, propyl group, isopropyl group, butyl group, isobutyl group, t-butyl group, amyl group, hexyl group, octyl group, decyl group and the like. Can be mentioned. Further, the alkoxy group having 1 to 10 carbon atoms is the same as described above.

  Specific examples of the amino group-containing alkoxysilane compound include aminopropyltrimethoxysilane, aminopropyltriethoxysilane, aminopropylmethyldimethoxysilane, N-aminoethyl-aminopropyltrimethoxysilane, and N-aminoethyl-aminopropylmethyldimethoxy. Silane, N-aminoethyl-aminopropyltriethoxysilane, ureidopropylpropyltrimethoxysilane, anilinopropyltrimethoxysilane, N-phenyl-aminopropyltrimethoxysilane, and the like. Two or more kinds can be used. Preferably, aminopropyltrimethoxysilane, aminopropyltriethoxysilane, N-aminoethyl-aminopropyltrimethoxysilane, N-aminoethyl-aminopropyltriethoxysilane, ureidopropylpropyltrimethoxysilane, anilinopropyltrimethoxysilane , Trialkoxysilanes such as N-phenyl-aminopropyltrimethoxysilane. More preferred is aminopropyltrimethoxysilane or aminopropyltriethoxysilane.

  The amino group-containing alkoxysilane compound is used after diluted in a solvent. Solvents include water, methanol, ethanol, isopropanol, carbitol, cellosolve, ethylene glycol, acetone, hexane, methyl ethyl ketone, hexane, ethyl acetate, methyl benzoate, diethyl phthalate, diethyl adipate, dibutyl ether, anisole, benzene, Toluene, xylene and the like can be mentioned, and one or more of these solvents can be used. The concentration of the amino group-containing alkoxysilane compound is 0.01 to 10% by weight, more preferably 0.1 to 5% by weight. This is because if it exceeds 10% by weight, the liquid becomes unstable and precipitation occurs. Moreover, it is because sufficient effect will not be acquired when it is less than 0.01 weight%.

  In the present invention, a triazine thiol derivative represented by the following general formula (2) is used.

Here, R3 represents a monovalent aliphatic hydrocarbon group having 1 to 4 carbon atoms which may have a substituent, a monovalent aromatic hydrocarbon group which may have a substituent, or a hydrogen atom. To express. R4 represents a C1-C20 divalent aliphatic hydrocarbon group which may have a substituent, and the aliphatic hydrocarbon group may include a hetero atom or a functional group. Preferably, the aliphatic hydrocarbon group contains a hetero atom or a functional group, and the hetero atom or functional group is preferably a divalent sulfur atom, a divalent nitrogen atom, a carbamoyloxy group or a urea group. By including a hetero atom or a functional group, the triazine thiol derivative is easily arranged on the surface of the solid material, and the reactive group can be more uniformly distributed. X ² represents a monovalent aliphatic hydrocarbon group having 1 to 20 carbon atoms which may have a substituent. Y ² represents an alkoxy group having 1 to 10 carbon atoms. n represents a natural number of 1 to 3. M represents a hydrogen atom or an alkali metal.

Here, examples of R3 include a hydrogen atom, a methyl group, a propyl group, an allyl group, a butyl group, a phenyl group, and a cyclohexyl group. As the _{R4, -CH 2 CH 2 -,} - (CH 2) 6 -, - (CH 2) 10 -, - CH 2 CH 2 SCH 2 CH 2 -, - CH 2 CH 2 CH 2 SCH 2 CH _{2 CH 2 -, - CH 2} CH 2 NHCH 2 CH 2 CH 2 -, - (CH 2 CH 2) 2 NCH 2 CH 2 CH 2 -, - C 6 H 4 -, - C 6 H 4 C 6 H 4 _{-, - CH 2 C 6 H} 4 CH 2 -, - CH 2 CH 2 OCONHCH 2 CH 2 CH 2 -, - CH 2 CH 2 NHCONHCH 2 CH 2 CH 2 -, or _{- (CH 2 CH 2) 2} CHOCONHCH 2 CH ₂ CH ₂ — and the like can be mentioned. Examples of X ² include a hydrogen atom, a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, an isobutyl group, and a t-butyl group. N represents a natural number of 1 to 3. M is a hydrogen atom, Li, Na, K, or Ce.

  Moreover, as a substituent which said aliphatic hydrocarbon and aromatic hydrocarbon may have, a C1-C10 alkyl group and a C1-C10 alkoxy group can be mentioned. Here, the alkyl group having 1 to 10 carbon atoms includes methyl group, ethyl group, propyl group, isopropyl group, butyl group, isobutyl group, t-butyl group, amyl group, hexyl group, octyl group, decyl group and the like. Can be mentioned. Further, the alkoxy group having 1 to 10 carbon atoms is the same as described above.

  Specific examples of the triazine thiol derivative include 6- (triethoxysilane) propylamino-1,3,5-triazine-4,6-dithiol monosodium), 6- (trimethoxysilane) propylamino-1,3, Examples include 5-triazine-4,6-dithiol monosodium, 6- (triethoxysilane) ethylamino-1,3,5-triazine-4,6-dithiol monosodium, and the like.

  Solvents include water, methanol, ethanol, isopropanol, carbitol, cellosolve, ethylene glycol, acetone, hexane, methyl ethyl ketone, hexane, ethyl acetate, methyl benzoate, diethyl phthalate, diethyl adipate, dibutyl ether, anisole, benzene, Toluene, xylene and the like can be mentioned, and one or more of these solvents can be used. The concentration of the triazine thiol derivative is 0.01 to 10% by weight, more preferably 0.1 to 5% by weight. This is because if it exceeds 10% by weight, the liquid becomes unstable and precipitation occurs. Moreover, when it is less than 0.01% by weight, a sufficient effect cannot be obtained.

(Formation of reactive solid surface)
The forming method of the present invention includes a step of attaching an amino group-containing alkoxysilane compound to the surface of a solid material having a resin layer on at least a surface, and then a step of attaching a triazine thiol derivative to the surface of the solid material.

  Unless a resin is used for the solid material, it is necessary to form a resin layer on the surface of the solid material. The thickness of the resin layer is desirably 10 nm or more. This is because if it is smaller than 10 nm, it is difficult to bind the amino group-containing alkoxysilane compound.

  The method for forming the resin layer is not particularly limited. If the resin is in the form of a film, it can be formed by a method such as pressure bonding or thermocompression bonding, a coating method if the resin is soluble in a solvent, and a vapor deposition method if insoluble in the solvent and vapor deposition. For the resin layer, a resin having no hydroxyl group in the constituent monomer unit is used.

  In the step of attaching the amino group-containing alkoxysilane compound (hereinafter referred to as APS attachment step), a solution containing the amino group-containing alkoxysilane compound is brought into contact with the surface of the solid material and then heated. As the contact method, for example, methods such as dipping, coating, spraying and the like can be used. Immersion is preferred because it can be uniformly contacted with the solution. Although immersion conditions are not specifically limited, It is preferable to immerse for 1 minute-60 minutes at the temperature of 10 to 60 degreeC. As heating conditions, it is preferable to heat at a temperature of 40 to 250 ° C. for 1 second to 30 minutes. The heating method is not particularly limited, and a known method can be used. For example, an oven, a dryer, high frequency heating, or the like can be used. In addition, in order to fully react an amino-group-containing alkoxysilane compound with a resin layer, you may repeat said contact and heating in multiple times as needed.

  In the step of attaching the triazine thiol derivative (hereinafter referred to as the TES attachment step), after the APS attachment step, the surface of the solid material is further brought into contact with a solution containing the triazine thiol derivative, and then heated. As the contact method, for example, methods such as dipping, coating, spraying and the like can be used. Immersion is preferred because it can be uniformly contacted with the solution. Although immersion conditions are not specifically limited, It is preferable to immerse for 1 minute-60 minutes at the temperature of 0 to 100 degreeC. As heating conditions, it is preferable to heat at a temperature of 40 to 250 ° C. for 1 second to 30 minutes. The heating method is not particularly limited, and a known method can be used. For example, an oven, a dryer, high frequency heating, or the like can be used. In addition, in order to fully react a triazine thiol derivative with an amino group containing alkoxysilane compound, you may repeat said contact and heating in multiple times as needed.

(Reaction between reactive solid surface and different materials)
The reactive solid surface produced by the above method can be reacted with rubber, metal or ceramics.

(Reaction with rubber)
Rubber can be bonded to the reactive solid surface by thermocompression bonding. Specifically, an uncrosslinked rubber compound is thermocompression bonded to the surface of the reactive solid. The composition of uncrosslinked rubber comprises rubber materials, fillers, crosslinking agents, crosslinking accelerators, metal activators as essential components, and stabilizers, anti-aging agents, UV inhibitors, softeners, colorants, as necessary. Add retarder or the like.

  Examples of rubber materials include soft polyvinyl chloride, chlorinated polyethylene, chlorosulfonated polyethylene, alkylated chlorosulfonated polyethylene, chloroprene rubber, chlorinated acrylic rubber, brominated acrylic rubber, fluororubber, epichlorohydrin and copolymer rubber thereof. , Chlorinated ethylene propylene rubber, chlorinated butyl rubber, brominated butyl rubber, natural rubber, isoprene rubber, butadiene rubber, styrene-butadiene rubber, acrylonitrile-butadiene rubber, butyl rubber, ethylene-propylene rubber, ethylene-propylene-diene rubber, acrylic rubber, Examples include ethylene-acrylic rubber, urethane rubber, hydrogenated acrylonitrile-butadiene rubber, hydrogenated chloroprene rubber, and three-dimensional crosslinked rubber obtained by crosslinking hydrogenated styrene-butadiene rubber. Rukoto can.

  Examples of the filler include various grades of carbon black such as HAF and FEF, silica, nippil, talc, calcium silicate, calcium carbonate, carbon fiber, polyester fiber, and glass fiber. The amount of the filler used is 1 to 200 parts by weight, more preferably 20 to 80 parts by weight, based on 100 parts by weight of the rubber material.

  As crosslinking agents, triazine trithiol, 2-dibutylamino-1,3,5-triazine-4,6-dithiol, ethylenethiourea, bisphenol A, sulfur, colloidal sulfur, dicumyl peroxide, di-t-butyl peroxide, 2, Peroxidation of 5-dimethyl-2,5-di (t-butylperoxy) hexane, 2,5-dimethyl-2,5- (t-butylperoxy) hexyne-3, di (t-butylperoxyisopropyl) benzene, etc. 0.1 to 10 parts by weight, preferably 0.5 to 5 parts by weight of the product, benzoquinone dioxime, zarigen, dimethylol / phenol, etc. are added. If the amount is less than 0.1 part by weight, the crosslinking is insufficient and the elastic body is not formed. If the amount is more than 10 parts by weight, the degree of crosslinking is too high and the elastic body becomes a hard elastic body and the airtightness and the sealing performance are lowered.

  In order to promote crosslinking, azoles such as dibenzothiazoyl disulfide, 4-morpholinodithiothiothiazole, N-cyclohexyl-2-benzothiazoylsulfenamide, Nt-butyl-2-benzothiazoylsulfenamide, Sulfenamides such as N-oxydiethylene-2-benzothiazoyl sulfenamide, N-diisopropyl-2-benzothiazoyl sulfenamide, N-dicyclohexyl-2-benzothiazoyl sulfenamide, tetramethyl 0.1 to 10 parts by weight, preferably 0.5 to 5 parts by weight, of a turum-based cross-linking accelerator such as a turum disulfide, a tetraethylturum disulfide, a tetrabutylturum disulfide, or a tetraoctylturum disulfide is added. If the amount is less than 0.1 parts by weight, the crosslinking is insufficient and the elastic body is not sufficient. If the amount is more than 10 parts by weight, the degree of crosslinking is too high and the elastic body is hard, and the airtightness and sealing performance are lowered. .

  Zinc oxide, magnesium oxide, calcium oxide, barium oxide, aluminum oxide, tin oxide, iron oxide, calcium hydroxide, calcium carbonate, magnesium carbonate, fatty acid sodium, calcium octylate for the purpose of adjusting the crosslinking rate and accepting acid 0.1 to 20 parts by weight, preferably 1 to 10 parts by weight of a metal activator such as potassium isooctylate, potassium butoxide, cesium octylate or potassium isostearate is added. If the amount is less than 1 part by weight, a sufficient effect cannot be obtained. If the amount is more than 20 parts by weight, the properties of the rubber change and desired characteristics cannot be obtained.

  The above-mentioned uncrosslinked rubber compound is used after being formed into a sheet by mixing with a Banbury mixer and blending with a roll.

  The uncrosslinked rubber compound thus obtained is brought into contact with the surface of the reactive solid, and an adhesive is obtained by heating at 40 to 200 ° C. for 1 to 60 minutes under a pressure of 0.1 to 3 MPa. Can do.

(Reaction with metals)
The reactive solid surface obtained by the present invention has a thiol group as a reactive group, and this thiol group is chemically bonded to a metal serving as a catalyst for electroless plating such as palladium, platinum, or silver. Accordingly, various metals can be bonded onto the surface of the reactive solid by using electroless plating.

  Specifically, the surface of the reactive solid is immersed in the catalyst solution to adhere the catalyst. As the catalyst solution, an aqueous solution containing a palladium salt, a platinum salt, a silver salt, tin chloride or the like is used.

  Next, when the surface of the reactive solid carrying the catalyst is immersed in the electroless plating solution, only the portion where the catalyst exists is plated to form a metal layer.

  The electroless plating solution should contain a metal salt and a reducing agent as the main components, and added with auxiliary components such as a pH adjuster, buffer, complexing agent, accelerator, stabilizer and improver. it can. Examples of metals that can be electrolessly plated include gold, silver, copper, nickel, cobalt, iron, palladium, platinum, brass, molybdenum, and tungsten, and these metal salts are used.

Specific metal _{salts, AuCN, Ag (NH 3)} 2 NO 3, AgCN, CuSO 4 · 5H 2 O, CuEDTA, NiSO 4 · 7H 2 O, NiCl 2, Ni (OCOCH 3) 2, CoSO 4, Examples thereof include CoCl ₂ and PdCl ₂ .

Reducing agents are those having an effect of generating a metal by reducing the metal _{salts, KBH 4, NaBH 4, NaH} 2 PO 2, (CH 3) 2 NH · BH 3, CH 2 O, NH 2 NH ₂ , hydroxyamine salt, N, N-ethylglycine and the like can be mentioned. The concentration is preferably in the range of 0.001 to 1 mol / L.

  The following auxiliary components may be added to the main components as described above for the purpose of extending the life of the electroless plating bath or increasing the reduction efficiency. Basic compounds, inorganic salts, organic acid salts, citrates, acetates, borates, carbonates, ammonia hydroxide, EDTA, diaminoethylene, sodium tartrate, ethylene glycol, thiourea, triazinethiol, triethanolamine, etc. It is. The concentration is preferably in the range of 0.001 to 1 mol / L.

  The electroless plating is preferably performed in a temperature range of 0 to 98 ° C. and an immersion time of 1 to 300 minutes.

  By performing electroplating after electroless plating, a metal can be further deposited on the metal layer formed by electroless plating, and the metal layer can be made thicker. This is effective when it is necessary to lower the electrical resistance of the metal layer. Examples of the metal used for electroplating include Au, Ag, Pt, Cu, Ni, and Pd. Ag, Cu, or Ni is preferable.

  Hereinafter, the present invention will be described in more detail with reference to examples. In the examples, “parts” or “%” are based on weight unless otherwise specified. “Phr” means the number of parts of the additive with respect to 100 parts of the resin.

Example 1.
(Resin layer forming process)
On a soda glass substrate having a thickness of 0.7 mm and a size of 5 cm × 5 cm, as a resin material, a positive resist made of acrylic resin (PC-403: manufactured by JSR) (composition: acrylic resin (acrylamide having carbonyl group and acrylamide group) (Methacrylamide), naphthoquinone diad sulfonic acid ester, coupling agent, diethylene glycol methyl ethyl ether) was applied to a thickness of 500 nm by a spin coater to form a resin film on the substrate (hereinafter referred to as a substrate with a resin film). .) In addition, this resin film material can be made into a predetermined pattern shape by exposing to ultraviolet rays through a photomask having a predetermined pattern and then developing with alkali.

(APS adhesion process)
A 2% solution of aminopropyltriethoxysilane was prepared using hexane as a solvent. The substrate with the resin film was immersed in this solution (20 ° C., 10 minutes), and then heated in an oven at 80 ° C. As a result, aminopropyltriethoxysilane was adhered to the surface of the resin film.

(TES adhesion process)
As the triazine thiol derivative, 6- (triethoxysilane) propylamino-1,3,5-triazine-4,6-dithiol monosodium) was used. Using a mixed solution of ethanol 95% / water 5% as a solvent, a 0.1% solution of this triazine compound was prepared. A substrate with a resin film treated with an amino group-containing alkoxysilane compound was immersed in this solution (room temperature, 20 seconds) and heated at 180 ° C. in an oven. As a result, the triazine thiol derivative was adhered to the surface of the resin film to obtain a substrate having a reactive solid surface.

(Surface analysis)
When the surface after the APS adhesion process and the surface after the TES adhesion process was analyzed by XPS (X-ray photoelectron spectroscopy), an Si2p peak based on APS-derived silicon and an S2p peak based on TES-derived sulfur were confirmed. For comparison, an untreated resin substrate and a substrate surface subjected to only the TES deposition step without performing the APS deposition step were analyzed by XPS, and no sulfur-based peak was confirmed from any substrate. From this result, it can be seen that aminopropyltriethoxysilane and the triazine thiol derivative are bonded.

Example 2
(Reaction with rubber)
BR (butadiene rubber, manufactured by Nippon Zeon, nipole BR) 100 phr, CB (SRF carbon black, manufactured by Asahi Carbon) 40 phr, sulfur 2 phr, stearic acid 1 phr, zinc oxide 5 phr, MBTS (DM, manufactured by Ouchi Shinsei Chemical Co., Ltd.) 1 phr was kneaded with a Banbury mixer and then formed into a sheet. This rubber sheet was placed on the surface of the reactive solid produced in Example 1, and heat-pressed under the conditions of 160 ° C., 10 minutes, and 0.98 MPa with a press. This rubber sheet could not be peeled from the substrate by hand.

Comparative Example 1
A substrate with a resin film was obtained in the same manner as in Example 1 except that the APS adhesion process was not performed and only the triazine thiol derivative treatment was performed. A rubber sheet was thermocompression bonded to this substrate in the same manner as in Example 2. The sheet adhered to the substrate but could be easily peeled off by hand.

Comparative Example 2
A substrate with a resin film was obtained in the same manner as in Example 1 except that only the APS adhesion process was performed without performing the TES adhesion process. A rubber sheet was thermocompression bonded to this substrate in the same manner as in Example 2. The sheet adhered to the substrate but could be easily peeled off by hand.

Comparative Example 3
A substrate with a resin film was obtained in the same manner as in Example 1 except that the TES attaching step and the APS attaching step were performed. A rubber sheet was thermocompression bonded to this substrate in the same manner as in Example 2. The sheet adhered to the substrate but could be easily peeled off by hand.

Example 3 FIG.
(Reaction with metals)
On the reactive solid surface produced in Example 1, the plating film which consists of copper was produced by the electroless-plating method. Specifically, the following procedure was used.
(1) Pre-dip treatment (immersion at 25 ° C. for 1 minute, cataplet 404 (manufactured by Rohm and Haas))
(2) Catalyzing treatment (immersion at 80 ° C. for 1 minute, mixed liquid of cataplet 404 and cataposit 44 (Rohm and Haas))
(3) Rinsing with water (4) Accelerate treatment (immersion 25 ° C., 10 minutes, accelerator 19E (Rohm and Haas))
(5) Rinsing with water (6) Electroless copper plating treatment (immersion 25 ° C., 20 minutes, Sulcup PSY (manufactured by Uemura Kogyo Co., Ltd.))
(7) Water rinsing (8) Replacement gold plating treatment (immersion at 80 ° C for 5 minutes, NC Gold BS (manufactured by Kojima Chemical Co., Ltd.))
(9) Water rinse (10) Firing (150 ° C., 10 minutes in oven)

(Tape peeling test)
A polyimide tape (manufactured by ASONE, model number 1-6797-01, adhesive strength: 5.69 N / 25 mm) was used as the tape. After the plating film was cut into a 1 mm square grid, this tape was applied and peeled off, but the plating film was not peeled off at all.

Comparative Example 4
A substrate with a resin film was obtained in the same manner as in Example 1 except that only the TES adhesion process was performed without performing the APS adhesion process. Electroless plating was performed on this substrate by the same method as in Example 3, but a plating film could not be formed.

Comparative Example 5
A substrate with a resin film was obtained in the same manner as in Example 1 except that only the APS adhesion process was performed without performing the TES adhesion process. Electroless plating was performed on this substrate by the same method as in Example 3, but a plating film could not be formed.

Comparative Example 6
A substrate with a resin film was obtained in the same manner as in Example 1 except that the APS adhesion step and the TES adhesion step were not performed. Electroless plating was performed on this substrate by the same method as in Example 3, but a plating film could not be formed.

Example 4
(Example of different resin layers)
On the same soda glass substrate as in Example 1, a urethane resin (371G: manufactured by Techno Alpha) was pattern printed as a resin material by screen printing. After printing, it was dried on an 80 ° C. hot plate and baked in an oven at 150 ° C. for 1 hour to form a resin film. The thickness of the resin film was 500 nm.

(APS adhesion process)
A 2% solution of aminopropyltriethoxysilane was prepared using hexane as a solvent. The substrate with the resin film was immersed in this solution (20 ° C., 10 minutes), and then heated in an oven at 80 ° C. As a result, aminopropyltriethoxysilane was adhered to the surface of the resin film.

(TES adhesion process)
As the triazine thiol derivative, 6- (triethoxysilane) propylamino-1,3,5-triazine-4,6-dithiol monosodium) was used. Using a mixed solution of ethanol 95% / water 5% as a solvent, a 0.1% solution of this triazine compound was prepared. A substrate with a resin film treated with an amino group-containing alkoxysilane compound was immersed in this solution (room temperature, 20 seconds) and heated at 180 ° C. in an oven. As a result, the triazine thiol derivative was adhered to the surface of the resin film to obtain a substrate having a reactive solid surface.

(Surface analysis)
When the surface after the APS adhesion process and the surface after the TES adhesion process was analyzed by XPS (X-ray photoelectron spectroscopy), an Si2p peak based on APS-derived silicon and an S2p peak based on TES-derived sulfur were confirmed. For comparison, an untreated resin substrate and a substrate surface subjected to only the TES deposition step without performing the APS deposition step were analyzed by XPS, and no sulfur-based peak was confirmed from any substrate. From this result, it can be seen that aminopropyltriethoxysilane and the triazine thiol derivative are bonded.

Embodiment 5 FIG.
(Reaction with rubber)
BR (butadiene rubber, manufactured by Nippon Zeon, nipole BR) 100 phr, CB (SRF carbon black, manufactured by Asahi Carbon) 40 phr, sulfur 2 phr, stearic acid 1 phr, zinc oxide 5 phr, MBTS (DM, manufactured by Ouchi Shinsei Chemical Co., Ltd.) 1 phr was kneaded with a Banbury mixer and then formed into a sheet. This rubber sheet was placed on the surface of the reactive solid produced in Example 4, and thermocompression bonded under the conditions of 160 ° C., 10 minutes, and 0.98 MPa with a press. This rubber sheet could not be peeled from the substrate by hand.

Claims (4)

A step of attaching a compound represented by the general formula (1) to at least a solid surface having a resin layer on the surface, and a step of attaching a compound represented by the general formula (2) to the surface of the solid. Method for forming a reactive solid surface.

(Wherein R1 is a monovalent aliphatic hydrocarbon group having 1 to 20 carbon atoms which may have a substituent, a monovalent aromatic hydrocarbon group which may have a substituent, or R2 represents a hydrogen atom, which may have a substituent, a C1-C20 divalent aliphatic hydrocarbon group, a divalent aromatic hydrocarbon group that may have a substituent, or it represents a carbonyl group, an aliphatic hydrocarbon group which may contain a hetero atom or a functional group .X ¹ is a monovalent aliphatic hydrocarbon group having 1 to 20 carbon atoms that may have a substituent, A monovalent aromatic hydrocarbon group, a halogen atom or a hydrogen atom which may have a substituent, Y ¹ represents an alkoxy group having 1 to 10 carbon atoms, and n is a natural number of 1 to 3. is there.)

(In the formula, R 3 is a monovalent aliphatic hydrocarbon group having 1 to 4 carbon atoms which may have a substituent, a monovalent aromatic hydrocarbon group which may have a substituent, or a hydrogen atom. .R4 representing a represents a divalent aliphatic hydrocarbon group having 1 to 20 carbon atoms which may have a substituent group, the aliphatic hydrocarbon group may contain a hetero atom or a functional group .X ² Represents a monovalent aliphatic hydrocarbon group having 1 to 20 carbon atoms which may have a substituent, Y ² represents an alkoxy group having 1 to 10 carbon atoms, and n represents a natural number of 1 to 3. M represents a hydrogen atom or an alkali metal.)   The method according to claim 1, wherein the resin has a carbonyl group in at least one constituent monomer unit.   The formation method according to claim 1 or 2, wherein in the compound represented by the general formula (1), R1 is a hydrogen atom.   4. The compound represented by the general formula (1), wherein R 2 is a divalent aliphatic hydrocarbon group having 1 to 20 carbon atoms which may have a substituent. 5. Forming method.