JP4995480B2 - Composite molded body - Google Patents

Description

  The present invention relates to a composite molded body of a soft rubber and an organic resin. More specifically, the present invention relates to a composite molded body of soft rubber and polycarbonate resin that is integrally molded by injection molding or the like.

Conventionally, polycarbonate resin has made use of its characteristics such as impact resistance, heat resistance, high transparency, and light weight, and it has been developed for electronic devices such as CDs and mobile phones, OA equipment, medical equipment, automobile parts, building materials, and glasses. It has been used for various purposes such as and goggles, and its demand is expected to increase further in the future.
In addition to being used alone, polycarbonate resin is also used as a composite with flexibility for impact relaxation, sealing properties, etc., such as bonding with soft rubber or coating with soft rubber. Specific examples thereof include keypads and switches of various electronic devices such as mobile phones, mobile communication devices, game machines, watches, image receivers, optical / magnetic recording devices, seal portions, goggles, and the like.
As a soft rubber used for such a composite, a silicone rubber excellent in transparency and durability is well known. Among silicone rubbers, a liquid silicone having a liquid property before curing, a fast curability, and a good fluidity is suitable for injection molding and is advantageous for producing an inexpensive composite molded body. There has been proposed a silicone adhesive composition that can be integrally formed without a primer by adding a specific adhesion-imparting component (see Patent Document 1), and its application has been expanded.
However, since silicone rubber tends to have low adhesion to general adhesives and adhesive tapes, when using a composite molded product of silicone rubber and polycarbonate resin in combination with an adhesive or adhesive tape, Surface treatment or special adhesive may be required. When such secondary processing is required, it is said that the process load is large.
JP 2004-331820 A

  An object of the present invention is to provide a composite of a soft rubber and a polycarbonate resin, which is obtained by integral molding and has excellent secondary processability such as application of an adhesive or a pressure-sensitive adhesive tape.

  As a result of various studies, the present inventor has found that as a soft rubber component, (A) a polyoxyalkylene polymer having at least one alkenyl group on average in one molecule, (B) one on average in one molecule When using a compound having a hydrosilyl group exceeding (C) and a curable composition comprising a hydrosilylation catalyst as an essential component, when the polycarbonate resin is in contact with the polycarbonate resin in the course of curing when integrally molded with the polycarbonate resin, It has been found that it exhibits excellent adhesion and at the same time has excellent mold release properties for molding dies. Furthermore, it is found that a composite molded body in which a soft rubber excellent in secondary processability such as adhesion and adhesion and a polycarbonate resin is bonded can be obtained by curing it in a state where it is in contact with the polycarbonate resin. Completed.

  The composite molded body of the present invention is obtained by joining a polycarbonate resin excellent in impact resistance, heat resistance, and high transparency and a polyoxyalkylene rubber having high applicability to an adhesive or an adhesive tape. , OA equipment, medical equipment, automobile parts, building materials, glasses and goggles can be used in a wide range of applications. In particular, it is useful for keypads and switches, seals, goggles, etc. of various electronic devices such as mobile phones, mobile communication devices, game machines, watches, image receivers, optical / magnetic recording devices and the like.

There is no restriction | limiting in particular as a polyoxyalkylene type polymer which has at least 1 alkenyl group in 1 molecule which is (A) component of this invention, A various thing can be used. Specifically, the polymer main chain has a repeating unit represented by the general formula (1). General formula (1):
-R ¹ -O- (1)
(Wherein R ¹ is a divalent alkylene group)
R ¹ in the general formula (1) is preferably a linear or branched alkylene group having preferably 1 to 14 carbon atoms, more preferably 2 to 4 carbon atoms. Specific examples of the repeating unit represented by the general formula (1) 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- and the like. 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, from the viewpoint of availability and workability, a polymer having —CH ₂ CH (CH ₃ ) O— as the main repeating unit is preferred. The main chain of the polymer may contain a repeating unit other than the oxyalkylene group. In this case, the total of oxyalkylene units in the polymer is preferably 80% by weight or more, particularly 90% by weight or more.

  The structure of the polymer of component (A) may be a linear polymer, a branched polymer, or a mixture thereof. In order to obtain good elasticity, it is preferable to contain 50% by weight or more of a linear polymer.

  The molecular weight of the polymer of component (A) is preferably 1,000 to 70,000 in terms of number average molecular weight, more preferably 3,000 to 50,000, and particularly preferably 5,000 to 30,000. When the number average molecular weight is less than 1,000, the resulting cured product tends to be too brittle and may lack elasticity as a good rubber. On the other hand, if the number average molecular weight exceeds 50,000, the viscosity becomes too high, and the handling of the composition may be remarkably lowered. The number average molecular weight can be measured by various methods, but usually conversion from a terminal group analysis of a polyoxyalkylene polymer or measurement by a gel permeation chromatography (GPC) method is common. The preferable number average molecular weight illustrated here is a value measured by the GPC method.

Although there is no restriction | limiting in particular as an alkenyl group in (A) component, The alkenyl group shown by following General formula (2) is used suitably. General formula (2):
^{_{H 2 C = C (R 2}} ) - (2)
(Wherein R ² is hydrogen or a methyl group)
Although there is no restriction | limiting in particular as a coupling | bonding mode to the polyoxyalkylene type polymer of an alkenyl group, For example, the direct coupling | bonding of an alkenyl group, an ether bond, an ester bond, a carbonate bond, a urethane bond, a urea bond etc. are mentioned.

As a specific example of the polymer of the component (A), the general formula (3):
_{{H 2 C = C (R} 3) -R 4 -O} aR 5 (3)
(In the formula, R ³ is hydrogen or a methyl group, R ⁴ is a divalent hydrocarbon group having 1 to 20 carbon atoms, and one or more ether groups may be contained, R ⁵ is polyoxy An alkylene-based polymer residue, and a is a positive integer). R ⁴ is _{specifically, -CH 2 -, - CH 2} CH 2 -, - CH 2 CH 2 CH 2 -, - CH 2 CH (CH 3) CH 2 -, - CH 2 CH 2 CH 2 CH 2 —, —CH ₂ CH ₂ OCH ₂ CH ₂ —, —CH ₂ CH ₂ OCH ₂ CH ₂ CH ₂ — and the like can be mentioned. From the viewpoint of ease of synthesis, —CH ₂ — is preferable.

Other specific examples of the polymer of the component (A) include the general formula (4):
_{{H 2 C = C (R} 3) -R 4 -OC (= O)} aR 5 (4)
(Wherein R ³ , R ⁴ , R ⁵ and a are the same as above), and a polymer having an ester bond.

Further, the following general formula (5):
{H ₂ C = C (R ³ )} a R ⁵ (5)
(Wherein R ³ , R ^5, and a are the same as those described above). Furthermore, the following general formula (6):
_{{H 2 C = C (R} 3) -R 4 -OC (= O) O} aR 5 (6)
A polymer having a carbonate bond represented by the formula (wherein R ³ , R ⁴ , R ⁵ and a are the same as above) is also included.

  The polymerization method of the polyoxyalkylene polymer (A) is the usual polymerization method of oxyalkylene (anionic polymerization method using caustic alkali) disclosed in JP-A-50-13396, etc., and JP-A-50-149797. A polymerization method using a chain extension reaction method using this polymer as a starting material, a polymerization method using a cesium metal catalyst disclosed in Japanese Patent Application Laid-Open No. 7-179597, Japanese Patent Application Laid-Open No. 61-197631, Polymerization method using porphyrin / aluminum complex catalyst disclosed in JP-A-61-215622, JP-A-61-215623, JP-A-61-218632, disclosed in JP-B-46-27250 and JP-B-59-15336 A polymerization method using a composite metal cyanide complex catalyst, a catalyst comprising a polyphosphazene salt disclosed in JP-A-10-273512, etc. It can be obtained by that polymerization.

  Practically, a method using a double metal cyanide complex catalyst is preferable from the viewpoint of catalyst availability and polymerization stability. A known method can be used as a method for producing the double metal cyanide complex catalyst. For example, U.S. Pat. Nos. 3,278,457, 3,278,459, 5,891,818, 5,767,323, 5,767,323, 5,536,883 No. 5,482,908, No. 5,158,922, No. 4,472,560, No. 6,063,897, No. 5,891,818, No. 5,627,122, The methods described in JP-A-5,482,908, JP-A-5,470,813, JP-A-5,158,922 and the like are preferable.

  The synthesis method of the polyoxyalkylene polymer (A) having at least one alkenyl group in one molecule is a normal polymerization method for producing the polyoxyalkylene polymer (anionic polymerization method using caustic alkali). In addition to the chain extension reaction method using this polymer as a raw material, JP-A 61-197631, JP-A 61-215622, JP-A 61-215623, JP-A 61-218632, JP 46-27250 and JP-B-59-15336.

  Various methods can be used for introducing an alkenyl group into the polyoxyalkylene polymer. For example, it can be introduced by copolymerization of a monomer having an alkenyl group such as allyl glycidyl ether and an oxyalkylene monomer. In addition, by reacting an oxyalkylene polymer having a functional group such as a hydroxyl group or an alkoxide group on the main chain or side chain with an organic compound having a functional group and an alkenyl group reactive to these functional groups, Alkenyl groups can be introduced into the main chain or side chain. In particular, when an alkenyl group is present at the end of the main chain of the polymer, the effective network chain length in the cured product is increased, and thus a cured product having excellent mechanical properties can be obtained.

  Examples of the organic compound having a functional group and an alkenyl group having reactivity with the above functional group include those having 3 to 20 carbon atoms such as acrylic acid, methacrylic acid, vinyl acetate, acrylic acid chloride or acrylic acid bromide. Saturated fatty acid acid halide, acid anhydride, allyl chloroformate, allyl chloride, allyl bromide, vinyl (chloromethyl) benzene, allyl (chloromethyl) benzene, allyl (bromomethyl) benzene, allyl (chloromethyl) ether, allyl ( Chloromethoxy) benzene, 1-butenyl (chloromethyl) ether, 1-hexenyl (chloromethoxy) benzene, allyloxy (chloromethyl) benzene and the like.

  The alkenyl group should be present in an amount exceeding an average of 1 in one molecule of the polymer (A), preferably 5 or less. When the number of alkenyl groups contained in one molecule of the polymer (A) is 1 or less on average, the curability is insufficient and the resulting network structure is incomplete, and a good molded product is obtained. Absent. Further, when the number of alkenyl groups contained in one molecule increases, the network structure becomes too dense, so that the resulting molded product is hard and brittle, which is not preferable. In particular, when the number is 5 or more, the tendency becomes remarkable.

  The compound having a hydrosilyl group exceeding 1 on average in one molecule as the component (B) in the present invention can be used without particular limitation as long as it has a hydrosilyl group, but has a number average molecular weight of 400 to 3,000. The thing of 500-1,000 is more preferable. When the number average molecular weight is less than 400, it is volatilized at the time of heat curing and a sufficient cured product cannot be obtained, and when it exceeds 3,000, a sufficient curing rate cannot be obtained. Examples of such compounds include organohydrogenpolysiloxanes modified with organic groups from the standpoint of availability of raw materials and compatibility with the component (A). These (B) components are preferably those having good compatibility with the (A) component. In particular, when the viscosity of the whole system is low, use of a material having low compatibility may cause phase separation and cause poor curing. Specifically showing the structure of such an organohydrogenpolysiloxane, for example,

（式中、１＜ｂ＋ｃ≦４０、１＜ｂ≦２０、０＜ｃ≦３８である。Ｒは、主鎖の炭素数が２〜２０の炭化水素基であり、１個以上のフェニル基を含有してもよい）、

(In the formula, 1 <b + c ≦ 40, 1 <b ≦ 20, 0 <c ≦ 38. R is a hydrocarbon group having 2 to 20 carbon atoms in the main chain, and represents one or more phenyl groups. May be contained),

（式中、０≦ｄ＋ｅ≦４０、０≦ｄ≦２０、０＜ｅ≦３８である。Ｒは、主鎖の炭素数が２〜２０の炭化水素基であり、１個以上のフェニル基を含有してもよい）、又は、

(In the formula, 0 ≦ d + e ≦ 40, 0 ≦ d ≦ 20, and 0 <e ≦ 38. R is a hydrocarbon group having 2 to 20 carbon atoms in the main chain, and represents one or more phenyl groups. May be included), or

（式中、３≦ｆ＋ｇ≦２０、１＜ｆ≦２０、０＜ｇ≦１８である。Ｒは、主鎖の炭素数が２〜２０の炭化水素基であり、１個以上のフェニル基を含有してもよい）等で示される鎖状又は環状のもの等が挙げられる。
（Ａ）成分及び（Ｃ）成分との相溶性、又は、分散安定性および硬化速度が比較的良好な（Ｂ）成分を具体的に示すと、以下のものが挙げられる。

(In the formula, 3 ≦ f + g ≦ 20, 1 <f ≦ 20, 0 <g ≦ 18. R is a hydrocarbon group having 2 to 20 carbon atoms in the main chain, and represents one or more phenyl groups. Or a chain-like or cyclic group represented by
Specific examples of the (B) component having relatively good compatibility with the (A) component and the (C) component, or relatively good dispersion stability and curing speed include the following.

式中、１＜ｋ＋ｌ≦２０、１＜ｋ≦１９、０＜ｌ≦１８である。Ｒは炭素数８以上の炭化水素基である。

In the formula, 1 <k + l ≦ 20, 1 <k ≦ 19, and 0 <l ≦ 18. R is a hydrocarbon group having 8 or more carbon atoms.

  As a more specific example of the component (B), methyl hydrogen polysiloxane is used in order to ensure compatibility with the component (A) and to adjust the amount of SiH, α-olefin, styrene, α-methylstyrene, Examples include compounds modified with allyl alkyl ethers, allyl alkyl esters, allyl phenyl ethers, allyl phenyl esters, and the like, and examples include the following structures.

但し、１＜ｐ＋ｑ≦４０、１＜ｐ≦２０、０＜ｑ≦３８である。また、さらに好ましい例としては、１＜ｐ＋ｑ≦２０、１＜ｐ≦１９、０＜ｑ≦１８である。

However, 1 <p + q ≦ 40, 1 <p ≦ 20, and 0 <q ≦ 38. Further, more preferable examples are 1 <p + q ≦ 20, 1 <p ≦ 19, and 0 <q ≦ 18.

  The amount of the hydrosilyl group-containing compound as the component (B) in the present invention is such that [total amount of hydrosilyl groups in the component (B)] / [total amount of alkenyl groups in the component (A)] is 0.5 or more. Preferably, it is 0.7 or more. When [total amount of hydrosilyl groups in component (B)] / [total amount of alkenyl groups in component (A)] is less than 0.5, the resulting soft rubber portion has low crosslink density, and thus has high tackiness. Handling of the composite molded body becomes difficult. In addition, if [total amount of hydrosilyl groups in component (B)] becomes excessive compared to [total amount of alkenyl groups in component (A)], formation of a three-dimensional network skeleton becomes difficult, and similarly obtained It becomes difficult to handle the composite molded body. Thus, it is necessary to pay attention to both the lower limit and the upper limit for the amount of component (B) used.

It does not specifically limit as a hydrosilylation catalyst which is (C) component of this invention, Arbitrary things can be used. For example, solid platinum supported on a carrier such as chloroplatinic acid, platinum alone, alumina, silica, carbon black, etc .; platinum-vinylsiloxane complex {for example, Pt _X (ViMe ₂ SiOSiMe ₂ Vi) _y , Pt [(MeViSiO) ₄ ] _z }; platinum-phosphine complex {eg, Pt (PPh ₃ ) ₄ , Pt (PBu ₃ ) ₄ }; platinum-phosphite complex {eg, Pt [P (OPh) ₃ ] ₄ , Pt [P (OBu) ₃ ] ₄ (wherein Me represents a methyl group, Bu represents a butyl group, Vi represents a vinyl group, Ph represents a phenyl group, x, y and z represent integers), Pt ( acac) ₂ (However, acac represents acetylacetonato), also platinum described in U.S. Pat. No. 3,159,601 and 3,159,662 of Ashby et al - hydrocarbon complex, and Lam Platinum alcoholate catalysts described in reaux et al., U.S. Patent No. 3,220,972 may also be mentioned.
Examples of catalysts other than platinum compounds include RhCl (PPh ₃ ) ₃ , RhCl ₃ , Rh / Al ₂ O ₃ , RuCl ₃ , IrCl ₃ , FeCl ₃ , AlCl ₃ , PdCl ₂ .2H ₂ O, NiCl _2. , TiCl _{4 and the} like.

These catalysts may be used alone or in combination of two or more. From the viewpoint of catalytic activity, chloroplatinic acid, platinum-olefin complexes, platinum-vinylsiloxane complexes, Pt (acac) _{2 and the} like are preferable. Although there is no restriction | limiting in particular as a usage-amount of a catalyst, It is good to use in the range of 10 ^<-8 > ^-10 < ^-1 > mol with respect to ¹ mol of alkenyl groups in (A) component. Preferably, it is used in the range of 10 ⁻⁶ to 10 ⁻² mol. If it is less than 10 ⁻⁸ mol, the curing rate is slow and the curability is likely to be unstable. Conversely, when it exceeds 10 ⁻¹ mol, it is difficult to ensure the pot life, which is not preferable.
In the curable composition comprising the components (A) to (C) of the present invention, a storage stability improving agent can be used for the purpose of improving storage stability. The storage stability improver may be a normal stabilizer known as a storage stabilizer for the component (B) of the present invention, as long as it achieves the intended purpose, and is particularly limited. is not. Specifically, a compound containing an aliphatic unsaturated bond, an organic phosphorus compound, an organic sulfur compound, a nitrogen-containing compound, a tin compound, an organic peroxide, or the like can be preferably used. Specifically, 2-benzothiazolyl sulfide, benzothiazole, thiazole, dimethylacetylene dicarboxylate, diethylacetylene dicarboxylate, 2,6-di-t-butyl-4-methylphenol, butylhydroxyanisole, vitamin E, 2- (4-morphodinyldithio) benzothiazole, 3-methyl-1-buten-3-ol, acetylenically unsaturated group-containing organosiloxane, acetylene alcohol, 3-methyl-1-butyl-3-ol , Diallyl fumarate, diallyl maleate, diethyl fumarate, diethyl maleate, dimethyl maleate, 2-pentenenitrile, 2,3-dichloropropene, and the like, but are not limited thereto.

  Moreover, the adhesion imparting agent for improving the adhesiveness with respect to polycarbonate resin can be added to the curable composition which consists of (A)-(C) component of this invention as needed. Examples of the adhesion imparting agent include various silane coupling agents and epoxy resins. In particular, a silane coupling agent having a functional group such as an epoxy group, a methacryloyl group, or a vinyl group is easy to use because it has little influence on curability and has a large effect on expression of adhesiveness. However, silane coupling agents that can be used are not limited to these. Moreover, the catalyst for making a silyl group or an epoxy group react can be added together with a silane coupling agent and an epoxy resin. In their use, the impact on the hydrosilylation reaction must be considered.

  In addition, various fillers, antioxidants, ultraviolet absorbers, pigments, surfactants, solvents, and silicon compounds may be appropriately added to the curable composition comprising the components (A) to (C) of the present invention. Good. Specific examples of the filler include silica fine powder, calcium carbonate, carbon black, clay, talc, titanium oxide, zinc white, diatomaceous earth, barium sulfate and the like.

  Moreover, as a polycarbonate resin used for the composite of the present invention, a commercially available polycarbonate resin can be used. In addition, a resin modifier, an inorganic filler, an organic filler, and various additives mixed and molded for the purpose of imparting various performances can be used.

  As a method for obtaining the composite molded article of the present invention, a liquid composition in which the components (A) to (C) and, if necessary, additives and fillers are uniformly mixed (hereinafter referred to as the liquid composition of the present invention). ) Is not particularly limited as long as it is cured in contact with the polycarbonate resin. For example, a composite molded article can be obtained even under conditions where no pressure is applied, such as applying the liquid composition to the surface of a polycarbonate resin and curing it with a hot air drier. It is also possible to obtain a composite molded body by fixing a polycarbonate resin to a press mold, filling the liquid composition of the present invention from above, and performing hot pressing. Furthermore, as an insert molding using an injection molding machine, a method of injecting the liquid composition of the present invention onto a polycarbonate resin fixed to an injection mold and molding the same is also possible. Also, methods such as compression molding, transfer molding, extrusion molding, and injection molding are possible.

  Further, in these various molding methods, the liquid composition of the present invention can be handled as a one-liquid form including all the components, or the two components can be mixed so that the components (B) and (C) are not mixed. It is also possible to treat it as a two-liquid form distributed to each other. In the former case, since the reaction can proceed gradually even at room temperature, storage at a low temperature is required, but the trouble of mixing two liquids at the time of molding can be omitted. In the latter case, it is necessary to mix the two liquids at the time of molding and apply, fill, and inject in a state that does not contain bubbles, but it is advantageous for long-term storage of the liquid composition. . Such a two-component liquid composition is used for a two-component mixing and discharging device used in a liquid injection molding system developed for liquid silicone, a two-component urethane resin, and an epoxy resin. The two-liquid mixing / discharging device can be used. Among these, the liquid injection molding system is an automated molding system in which the process from the supply of the two-component composition to the injection molding is integrated, and a composite molded product of the liquid composition of the present invention and the polycarbonate resin is obtained. Is a suitable molding method.

  Moreover, as a method of obtaining the liquid composition of this invention, (A)-(C) component and the method of mixing various additives and fillers used as needed using a mixer, a roll, a kneader, etc. Is mentioned. When there are a lot of moisture contained in the various compounding agents to be used, it is desirable to remove moisture as much as possible in order that the component (B) reacts with moisture to easily generate voids in the molded body. Furthermore, a composite molded body with few defects such as voids can be obtained by performing the defoaming treatment.

  The composite molded body of the polyoxyalkylene rubber and polycarbonate resin of the present invention is a composite of a hard resin and a soft rubber excellent in impact resistance, heat resistance and high transparency. It can be used for a wide range of applications including keypads, switches, seals, goggles, etc. of various electronic devices such as electronic devices, watches, image receivers, optical and magnetic recording devices.

  Next, although the composite molded object of this invention is demonstrated concretely according to an Example, this invention is not limited only to these Examples.

(Production Example 1)
Propylene oxide was polymerized using polypropylene glycol as an initiator and a zinc hexacyanocobaltate glyme complex catalyst to obtain a hydroxyl group-terminated polyoxypropylene polymer having a number average molecular weight of about 10,000 (measured by GPC method). Subsequently, the end of the hydroxyl group-terminated polyoxypropylene polymer was converted to an allyl group by adding 1.2 times equivalent of a 28% methanol solution of NaOMe and allyl chloride to the hydroxyl group. This reaction product was dissolved in hexane and adsorbed with aluminum silicate, and then the hexane was removed under reduced pressure to give a yellow transparent, polyoxypropylene polymer having an average of two allyl group ends in one molecule (A -1) was obtained.

(Production Example 2)
In the presence of a platinum catalyst, 0.5 equivalent of α-methylstyrene of the total amount of hydrosilyl groups is added to methylhydrogen silicone having an average of 10 (-Si-O-) repeating units, and an average of 5 per molecule. A compound (B-1) having a hydrosilyl group was obtained. The Si—H group content of this compound was 3.8 mmol / g.

(Production Example 3)
In the presence of a platinum catalyst, 0.2 equivalent of α-methylstyrene of the total amount of hydrosilyl groups was added to methylhydrogen silicone having an average of (—Si—O—) repeating units of 7.5, and the average per molecule A compound (B-2) having 6 hydrosilyl groups was obtained. The Si—H group content of this compound was 8.1 mmol / g.

Example 1
According to the blending amounts shown in Table 1, allyl group-terminated polyoxyalkylene polymer (A-1) obtained in Production Example 1, hydrosilyl compounds (B-1, B-2) and hindered phenols as component (B) A system antioxidant (Irganox 245 manufactured by Ciba Geigy), platinum vinylsiloxane (3% platinum xylene solution), and acetylene alcohol (Shinfin Chemical Co., Surfynol 61) were mixed.

  The liquid compositions (1-1, 1-2) thus obtained were each degassed and then filled onto a polycarbonate sheet (Mitsubishi Engineering Plastics Iupilon sheet, thickness 2 mm) and subjected to press molding. Molding was performed at 120 ° C. for 5 minutes. The obtained composite molded body was a composite molded body (molded bodies 1-1 and 1-2) in which a 1 mm thick polyoxyalkylene rubber was bonded to the surface of a 2 mm thick polycarbonate sheet.

(Example 2)
According to the blending amounts shown in Table 2, the allyl group-terminated polyoxyalkylene polymer (A-1) obtained in Production Example 1, a hindered phenol antioxidant (Irganox 245 manufactured by Ciba Geigy), wet silica (bulk specific gravity) 70 g / l) or fumed silica (bulk specific gravity 40 g / l) was mixed and dehydrated by heating. Subsequently, according to the blending amount shown in Table 2, as component (B), hydrosilyl compounds (B-1, B-2), platinum vinylsiloxane (3% platinum xylene solution), acetylene alcohol (Shinfin Chemical Industries Surfynol 61) ) Was mixed.

  The liquid composition (2-1, 2-2) thus obtained was subjected to the same method as described in Example 1 to form a composite molded body of a polyoxyalkylene rubber and a polycarbonate resin (molded body 2-1, 2-2) was obtained.

(Example 3)
The liquid composition 2-1 described in Example 2 was degassed and then filled on a polycarbonate sheet (Mitsubishi Engineering Plastics Iupilon sheet, thickness 2 mm), and 120 ° C., 5 ° C. without applying pressure on the press plate. By heating for a minute, a composite molded body (molded body 3) of polyoxyalkylene rubber and polycarbonate resin was obtained.

（参考例）
実施例２と同様に、実施例２記載の液状組成物２−１を実施例１記載と同様の方法により、厚さ２ｍｍのアクリル樹脂、ポリブチレンテレフタレート樹脂、ポリアセタール樹脂、ナイロン６樹脂、ナイロン６６樹脂、ポリフェニレンオキサイド樹脂上に、１ｍｍ厚のポリオキシアルキレン系ゴムを成形したが、いずれも密着力が弱く、容易に手で剥離した。このように、本発明のポリオキシアルキレン系ゴムとポリカーボネート樹脂との組み合わせにおいて、特異的に密着力の強い複合成形体が得られることがわかった。

(Reference example)
In the same manner as in Example 2, the liquid composition 2-1 described in Example 2 was treated in the same manner as described in Example 1 with a 2 mm thick acrylic resin, polybutylene terephthalate resin, polyacetal resin, nylon 6 resin, nylon 66. A 1 mm-thick polyoxyalkylene rubber was molded on the resin and the polyphenylene oxide resin, but they all had weak adhesion and were easily peeled by hand. As described above, it was found that a composite molded article having a particularly strong adhesive force can be obtained by the combination of the polyoxyalkylene rubber of the present invention and the polycarbonate resin.

(Adhesion test 1 of the composite molded product of the present invention)
In order to investigate the adhesion between the polyoxyalkylene rubber and the polycarbonate resin in the composite molded bodies (molded bodies 1-1, 1-2 and 2-1, 2-2) thus obtained, a hand peel test was conducted. went.

  As a result, in any composite molded body, the polyoxyalkylene rubber was agglomerated and destroyed, and it was confirmed that the polyoxyalkylene rubber and the polycarbonate resin had good adhesion.

(Adhesion test 2 of the composite molded product of the present invention)
Next, in order to examine the adhesion between the polyoxyalkylene rubber and the polycarbonate resin in the composite molded body (molded bodies 2-1 and 2-2) obtained in Example 2, a 180 ° peel test described in JIS K 6854 Went.

  As a result, in any composite molded article, the peel load was 20 N / 25 mm or more, and it was confirmed that the polyoxyalkylene rubber and the polycarbonate resin had good adhesion.

(Applicability of the adhesive to the soft rubber part of the composite molded body of the present invention)
The following various adhesives were applied to the surface of the composite molded body (2-1) obtained in Example 2 of the present invention, and an aluminum substrate and a polycarbonate substrate were attached. After curing for 1 week, a 180 ° peel test described in JIS K 6854 was performed. For comparison, a similar test was performed using silicone rubber having a hardness of Duro A 50 °.

1) Bond G Clear made by Konishi
2) Konishi Bond Silex White
3) Bondi Bond Ultra Versatile S / U Clear
4) Super X Clear made by Cemedine
5) Cemedine Loctite strong instantaneous adhesive The results are shown in Table 3.

表３に示されるように、本発明の複合成形体は、一部強力瞬間接着剤とアルミ基材との組み合わせにおいて密着力が発現していない例を除き、いずれもシリコーンゴムに比較し、良好な密着性を有していることが確認できた。

As shown in Table 3, the composite molded body of the present invention is good compared to silicone rubber, except for some examples where the adhesive strength is not expressed in the combination of a part of the strong instantaneous adhesive and the aluminum base. It was confirmed that it has excellent adhesion.

(Applicability of adhesive tape to the soft rubber part of the composite molded body of the present invention)
Next, two composite molded bodies (2-1) obtained in Example 2 of the present invention were attached with a double-sided adhesive tape, and a 180 ° peel test described in JIS K 6854 was performed. For comparison, a similar test was performed using silicone rubber having a hardness of Duro A 50 °.

  The results are shown in Table 4.

表４に示されるように、本発明の複合成形体はシリコーンゴムに比較し、粘着テープによる良好な密着性を有していることが確認できた。

As shown in Table 4, it was confirmed that the composite molded article of the present invention had better adhesion with an adhesive tape than silicone rubber.

Claims (3)

The following components (A) to (C) :
(A) a polyoxyalkylene polymer having a number average molecular weight of 1,000 to 70,000 and having an average of more than 1 and not more than 5 alkenyl groups in one molecule,
(B) a compound having an average of more than one hydrosilyl group in one molecule, and
(C) A polyoxyalkylene rubber / polycarbonate resin composite formed by laminating a polyoxyalkylene rubber obtained by curing a curable composition containing a hydrosilylation catalyst and a polycarbonate resin. A molded body ,
A composite molded article obtained by compression molding, transfer molding, extrusion molding, injection molding or injection molding in a state where the curable composition is in contact with a polycarbonate resin . The composite molded body according to claim 1, wherein an average structural formula of the compound having a hydrosilyl group as the component (B) is represented by the following general formula .

(Where a 1 <p + q ≦ 40,1 < p ≦ 20,0 <q ≦ 38.) The component for electronic devices which uses the composite molded object of Claim 1 or 2 .