JPH09164634A - Integrated molded object of thermoplastic polyester and silicone rubber - Google Patents

Abstract

PROBLEM TO BE SOLVED: To enhance hydrolysis resistance and heat ageing resistance by adding an oxidation inhibitor to polybutylene terephthalate using a Ti compd. as a polymerization catalyst and having a terminal COOH group in a concn. of a specific equivalent or less and compounding specific pts.wt. of an Si compd. and/or a polymer thereof with polybutylene terephthalate to integrate the same by a compsn. represented by a specific formula. SOLUTION: 0.05-3 pts.wt. (W) of an Si compd. having H directly bonded to Si and/or a polymer thereof is compounded with 100W of polybutylene terephthalate having a terminal COOH group in a concn. of 15 equivlent/ton or less and using a Ti compd. as a polymerization catalyst and 0.01-0.5W of a phenol type oxidation inhibitor and 0.01-0.5W of a thioether type oxidation inhibitor are compounded therewith and the resulting compd. is molded. A coating soln. containing organohydrogenpolysiloxane, a Pt compd. and a compsn. represented by formula (wherein R<1> is a substituted or non-substituted monovalent hydrocarbon group containing no aliphatic unsaturated bond and, when R<1> is plural, they may be different and (k) is 0 or an integer of 1 or more) is applied to the surface of the molded article to be cured.

Description

Detailed Description of the Invention

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a molded product in which a polybutylene terephthalate resin excellent in durability, particularly hydrolysis resistance and heat aging resistance, and silicone rubber are firmly integrated.

[0002]

2. Description of the Prior Art Thermoplastic polyester resins, especially polybutylene terephthalate, are widely used as industrial resins because of their excellent chemical resistance, heat resistance and mechanical properties. In recent years, with the increasing demands for hydrolysis resistance and heat aging resistance as durability, a silicone rubber that satisfies the above required properties in the electric / electronic field and the automobile field, and has excellent heat resistance, electrical properties, and weather resistance. It is desired to supply an integrally molded body that is firmly bonded.

Conventionally, as a method of adhering a molded product of an addition-curable silicone rubber and an organic resin, for example, a primer is applied to the surface of the molded product, an uncured silicone material is applied thereon, and the cured product is adhered. A method and a method of curing a self-adhesive silicone rubber material on a molding resin are known.

However, the method of bonding using a primer requires a complicated step of taking out the resin composition once molded from the mold and applying the primer.

Further, the method of applying a self-adhesive silicone rubber material to a molding resin and curing it is such that when a molded article and a silicone rubber are integrally formed using a mold or the like, the silicone rubber itself is There is a big problem that it adheres to the mold. Furthermore, when applied and cured to a resin molded product, most of self-adhesive addition-curable silicone rubber materials do not have an adhesive strength to a polybutylene terephthalate resin that can be used as an integrally molded product.

[0006]

DISCLOSURE OF THE INVENTION The present invention significantly improves the hydrolysis resistance and heat aging resistance of polybutylene terephthalate resin, which are increasing in demand as industrial resin materials.
In addition, the polybutylene terephthalate resin and the silicone rubber can be bonded easily and reliably in a short time, as well as the integrally molded product of the polybutylene terephthalate resin and the silicone rubber, which are adhered to each other with an adhesive strength that can withstand practical use. The purpose is to provide technology.

[0007]

The present inventors have arrived at the present invention as a result of intensive studies to solve the above-mentioned problems.

That is, according to the present invention, a titanium compound is used as a polymerization catalyst, and a phenol-based antioxidant and a thioether-based antioxidant are added to a polybutylene terephthalate resin having a low terminal carboxyl group concentration. Alternatively, by using the addition-curable silicone rubber containing an organopolysiloxane whose end is terminated by a trivinylsilyl group as an adhesiveness-imparting component, as a silicone rubber in which the polymer is blended and integrated on the other hand,
(EN) A silicone rubber integrated molded article (having a sufficient adhesive strength for practical use to a polybutylene terephthalate resin, which has conventionally been low in adhesive strength of an addition-curable silicone rubber or which could not be adhered in a short time) is obtained. In particular, the polybutylene terephthalate resin composition can be adhered to the above polybutylene terephthalate resin composition under a curing condition for a short time using an injection molding method, and the silicone rubber itself can be easily peeled from the molding die. It is the body.

The specific means of solution are: (a) (A) The terminal carboxyl concentration is 15 equivalents / ton.
In the following, per 100 parts by weight of polybutylene terephthalate using a titanium compound as a polymerization catalyst, (B) a silicon compound having a hydrogen atom directly bonded to at least one silicon atom in one molecule and / or a polymer thereof was added. 05-3
Parts by weight, (C) phenolic antioxidant 0.01 to 0.5
Parts by weight and (D) thioether antioxidant 0.01 to
On the surface of a molded article formed by molding a polybutylene terephthalate resin composition containing 0.5 parts by weight, (B) as an addition curable silicone rubber, (E) a vinyl group bonded to a silicon atom in one molecule. An organopolysiloxane having at least two, (F) an organohydrogenpolysiloxane having at least two hydrogen atoms bonded to silicon atoms in one molecule, (G) a platinum compound, and (H) the following general formula (1)

[0010]

Embedded image

(In the formula, R ¹ is a substituted or unsubstituted monovalent hydrocarbon group containing no aliphatic unsaturated bond, and when plural R ^1's are present, they may be different from each other.
Is an integer of 0 or 1 or more), and a coating solution comprising an organopolysiloxane composition containing a terminal trivinylsilyl-terminated organopolysiloxane represented by The resin molded product and the silicone rubber composition are in close contact with each other to form an integrally molded product.

Polybutylene terephthalate, which is the component (A) of the present invention, contains terephthalic acid as a main acid component,
It is a polyester containing 1,4-butanediol as a main glycol component. Here, “main” means 80 mol% or more, preferably 90 mol% or more, based on all acid components or all glycol components.

As the copolymerizable acid component, an aromatic dicarboxylic acid other than terephthalic acid, for example, isophthalic acid, naphthalene dicarboxylic acid, diphenyl dicarboxylic acid, diphenyl ether dicarboxylic acid, difoxyethane dicarboxylic acid, diphenyl ketone dicarboxylic acid, diphenyl sulfone. Examples thereof include dicarboxylic acids and the like, aliphatic dicarboxylic acids such as succinic acid, adipic acid and sebacic acid, and alicyclic dicarboxylic acids such as cyclohexanedicarboxylic acid, tetralindicarboxylic acid and decalindicarboxylic acid.

Copolymerizable glycol components other than butanediol include ethylene glycol hexamethylene glycol, neopentyl glycol, cyclohexanedimethanol, tricyclodecane dimethylol, xylylene glycol, bisphenol A, bisphenol B,
Examples thereof include bishydroxyethoxybisphenol A.

Further, monofunctional compounds such as glycerin, trimethylolpropane, pentaerythritol, trimellitic acid, trimesic acid and pyromellitic acid may be copolymerized within the range in which the polyester does not substantially lose the molding performance.

The polybutylene terephthalate used in the present invention must use a titanium compound as a polymerization catalyst, and the terminal carboxyl group concentration must be 15 equivalents / ton or less. Terminal carboxyl group concentration is 15 equivalents /
When it exceeds ton, the hydrolysis resistance, which is one of the main effects of the present invention, is not significantly improved. Further, when a tin compound is used as the polymerization catalyst, it is not preferable because it inhibits the curing of the silicone rubber.

The polybutylene terephthalate used in the present invention has an intrinsic viscosity (a value produced based on a measured value in orthochlorophenol at 35 ° C.) of 0.3 or more, preferably 0.5 or more. Is. When the intrinsic viscosity is lower than this, the strength is low, the viscosity is low, and it is difficult to use, and the meaning of applying the present invention is small.

The component (B) used in the present invention is a compound containing at least one silicon per minute and / or a polymer thereof, which is a SiH group-containing compound represented by the following formula.

[0019]

Embedded image (In the formula, m and n are 0 or an integer of 1 to 100, respectively.)

The phenolic antioxidant which is the component (C) used in the present invention is a hindered phenol compound.

The phenolic antioxidant is preferably 2,
6-di-t-butyl-p-cresol, 2,2'-methylene-bis- (4-methyl-6-di-t-butylphenol 4,4'-thiobis (3-methyl-t-butylphenol), 1 , 1,3-Tris (2-methyl-4-hydroxy-5-t-butylphenyl) butane, pentaerythrityl-tetrakis [3- (3,5-di-t-butyl-4-hydroxyphenyl) propionate] , Octadecyl-3- (3,5-di-t-butyl-4-hydroxyphenyl) propionate, and particularly preferably,
Pentaerythrityl-tetrakis [3- (3,5-di-
t-butyl-4-hydroxyphenyl) propionate].

One type or two or more types of phenol type antioxidants can be used at the same time. The blending amount of the phenolic antioxidant is required to be 0.01 to 0.5 parts by weight, preferably 0.1 to 1.3 parts by weight, based on 100 parts by weight of the polybutylene terephthalate resin. If the amount is less than 0.01 part by weight, the effect of improving the heat resistance is small and the result is 0.
Even if the amount is more than 5 parts by weight, the effect of improving the heat aging resistance cannot be expected.

Thio which is the component (D) used in the present invention
The ether antioxidant is preferably giteridyl-ti
Odipropionate, tetrakis [methylene-3-
(Dodecylthio) propionate], bis [2-methyl
-4- {3-n-alkyl (C ₁₂Or C₁₄) Thiopropi
Onyloxy} -5-t-butylphenyl] sulfide
It is.

The compounding amount of the thioether antioxidant is 0.0 with respect to 100 parts by weight of the polybutylene terephthalate resin.
1 to 0.5 parts by weight is necessary, and
0.3 parts by weight is preferred. If the amount is less than 0.01 part by weight, the effect of improving heat resistance cannot be expected.

Further, phosphorus-based antioxidants that are widely used as antioxidants should not be used because they inhibit the curing of silicone rubber.

The polybutylene terephthalate resin composition of the present invention may further contain a reinforcing material such as glass fiber, an inorganic filler, a pigment, a flame retardant, a flame retardant aid, a crystal nucleating agent and a light stabilizer. it can.

In the composition of the addition-curable silicone rubber used in the present invention, the vinyl group-containing organosiloxane as the component (E) has at least two vinyl groups bonded to silicon atoms in one molecule. . The molecular structure of the vinyl group-containing organopolysiloxane may be linear or branched, and even if the vinyl group exists only at the terminal of the molecule, it may be in the middle of the molecular chain. It may be present only at the end of the molecule or in the middle of the molecular chain. In particular, the following general formula:

[0028]

Embedded image

(In the formula, a plurality of R ^{2 to} R ⁸ may be the same or different and each is a substituted or unsubstituted monovalent hydrocarbon group containing no aliphatic unsaturated bond, and i is 0 or 1). ~ 100
And j is an integer of 0 or 1 or more. The diorganopolysiloxane having a vinyl group represented by the formula (1) is preferably used.

R ^{2 to} R ⁸ in the above general formula (3) are substituted or unsubstituted monovalent hydrocarbon groups having no aliphatic unsaturated bond, and are usually groups having 1 to 10 carbon atoms. And preferably a group having 1 to 6 carbon atoms. As R ^{2 to} R ⁸ , specifically, for example, an alkyl group such as a methyl group, an ethyl group, a propyl group, a butyl group;
An aryl group such as a tolyl group, a xylyl group, a benzyl group; for example, a cycloalkyl group such as a cyclohexyl group, a chloromethyl group obtained by substituting a part or all of hydrogen atoms of these groups with a substituent such as a halogen atom or a cyano group. And a cyanoethyl group 3,3,3-trifluoropropyl group and the like.

In the general formula (3), i is an integer of 1 to 100 including 0, j is 0 or an integer of 1 to 100, and i and j are preferably 0 <m + j <j. / (I
+ J) is an integer that satisfies 0.2.

The vinyl group-containing organopolysiloxane (E) has a viscosity at 25 ° C. of 10 to 1,000,
It is preferably 000 cSt (centistokes), and more preferably 100 to 10,000 cSt. The vinyl group-containing organopolysiloxane as the component (E) can be produced by a method known per se.

The organohydrogenpolysiloxane as the component (F) has at least two hydrogen atoms bonded to silicon atoms in one molecule. The component (B) acts as a crosslinking agent, and the composition of the present invention is cured by the addition reaction between the hydrogen atom bonded to the silicon atom and the vinyl group of the component (E). Is.

The molecular structure of the organohydrogenpolysiloxane of the component (F) is not particularly limited, and linear, branched or cyclic structures can be used. The viscosity of this organohydrogenpolysiloxane at 25 ° C. is usually 0.5 to 1000.
cSt, preferably 1 to 200 cSt.

Examples of the organohydrogenpolysiloxane as the component (F) include the following average composition formula (4):

[0036]

Embedded image H _a (R ⁹ ) _b SiO _{(4-ab) / 2} (4) (In the formula, R ⁹ is a substituted or unsubstituted monovalent hydrocarbon group containing no aliphatic unsaturated bond, a and b are 0 <a <
It is a number that satisfies 2, 1 ≦ b ≦ 2 and 2 ≦ a + b ≦ 3. ) Are suitably used.

A substituted or unsubstituted monovalent hydrocarbon group containing no aliphatic unsaturated bond represented by R ^{9 in} the above average composition formula (4) is usually a group having 1 to 10 carbon atoms, preferably Is a group of 1 to 7. Specific examples of R ⁹ include the groups exemplified as R ^{2 to} R ⁸ above.

Further, a and b are 0 <a <2,
It is a number satisfying 1 ≦ b ≦ 2 and 2 ≦ a + b ≦ 3, preferably 0.3 ≦ a ≦ 1 and 2 ≦ a + b ≦ 2.7.

The organohydrogenpolysiloxane as the component (F) can be produced by a method known per se, and is usually R ³ SiHCl ₂ , R ⁸ ₃ SiCl, R ⁸ _{2
^{SiCl 2, R 8 2 SiHCl,}} ( In the formulas, R ³ are as defined above.) Or a chlorosilane, such as hydrolysis,
Alternatively, it can be produced by equilibrating the siloxane thus obtained by hydrolysis.

Specific examples of the organohydrogenpolysiloxane as the component (F) include compounds represented by the following formula.

[0041]

[Chemical 6]

The blending amount of the organohydrogenpolysiloxane as the component (F) is not particularly limited, but is relative to one vinyl group bonded to a silicon atom contained in the component (E) and the component (H) described later. It is preferable to mix the organohydrogenpolysiloxane as the component (F) in an amount such that the number of hydrogen atoms bonded to silicon atoms is 1 to 5.

The platinum compound as the component (G) is an addition reaction catalyst, and the addition reaction between the vinyl group as the component (E) and the hydrogen atom bonded to the silicon atom of the organohydrogenpolysiloxane as the component (F) is carried out. It is used to promote.

As the platinum compound as the component (G),
Usually used as an addition reaction catalyst for organopolysiloxane compositions
Can be used. concrete
Contains platinum alone, and, for example, H_TwoPtCl₆・ XH
_TwoO, NaHPtCl₆・ XH_TwoO, KHPtCl₆・
XH_TwoO, Na_TwoPtCl₆・ XH_TwoO, K_TwoPtCl
₆・ XH_TwoO, PtCl_Four・ XH_TwoO, PtCl_Two, N
a_TwoPtCl_Four・ XH _TwoO, H_TwoPtCl_Four・ XH_TwoO
(Where X is a positive integer.)
I can do it. Further, with the platinum compound, for example, carbonized water
Complex with base, alcohol, vinyl group-containing cyclic siloxane, etc.
You can also use your body.

The amount of the platinum compound as the component (G) to be blended may be an amount sufficient to promote the addition reaction between the component (A) and the component (B). It is preferably 0.1 to 100 ppm in terms of platinum metal based on the total amount with the component (F).

The component (H) is a terminal trivinylsilyl-terminated organopolysiloxane represented by the above general formula (1). The composition of the present invention has a suitable pot life at room temperature by blending the component (H), and has good curability such that it cures rapidly when heated. Moreover, this (H) component can be manufactured by a well-known method.

In the above general formula (1), R ¹ is a substituted or unsubstituted monovalent hydrocarbon group containing no aliphatic unsaturated bond, preferably a group having 1 to 10 carbon atoms,
More preferably, it is a group of 1 to 7. Specific examples of R ¹ include lower alkyl groups such as methyl group, ethyl group and propyl group; aryl groups such as phenyl group, tolyl group, xylyl group and benzyl group; and cyclo groups such as cyclohexyl group. Alkyl group; chloromethyl group, cyanoethyl group, 3,3, in which a part or all of hydrogen atoms of these groups are substituted with a substituent such as a halogen atom and a cyano group.
Examples thereof include 3-trifluoropropyl group.

In the general formula (1), k is 0 or 1.
It is the above integer, preferably an integer of 0 to 100, and more preferably an integer of 0 to 20. Note that k is
Considering the compatibility of the component (H) with the component (E), it is preferably an integer of 0-20.

The compounding amount of the component (H) is 1 to 200 with respect to 1 mol of platinum metal contained in the platinum compound of the component (G).
The range of 00 mol is preferable, and the range of 10-500 mol is more preferable.

The practical use of the composition of the present invention
In addition to the components (E) to (H) described above, the curing of the present invention is impaired.
Add various additives as needed within the range not touched.
be able to. For example, a composition of the invention may include
Supplements the strength of the cured product obtained by curing the composition.
SiO to strengthen_TwoUnit, (CH_Two= CH) R ' _Two
SiO_0.5Unit, and R '_TwoSiO_0.5Units (where
R'is a monovalent hydrocarbon group containing no aliphatic unsaturated bond
is there. ) Organopolysiloxane consisting of
(Japanese Patent Publication No. 38-36771, Japanese Patent Publication No. 45-9476)
(See the official gazette), etc. can be added.
However, even if all the silicon atoms contained in the composition are bound,
Hydrogen atom bonded to silicon atom for one vinyl group
It is necessary to have 1 to 5 children.

Further, the composition of the present invention reduces the heat shrinkage during curing, decreases the thermal expansion coefficient of the elastic body obtained by curing, thermal stability, weather resistance, chemical resistance, flame retardancy, mechanical properties. A filler may be added for the purpose of improving the mechanical strength and lowering the gas permeability. Examples of such fillers include fumed silica; quartz powder; glass fiber; carbon black; metal compounds such as alumina, iron oxide, and titanium oxide; metal carbonates such as calcium carbonate and magnesium carbonate. Suitable pigments, if necessary,
It is also possible to add dyes, antioxidants and the like. The filler is usually the organopolysiloxane 100 as the component (E).
5 to 200 parts by weight are blended per part by weight.

The composition of the addition-curable silicone rubber of the present invention is usually prepared by separately packaging the mixture of the components (E) and (G) and the mixture of the components (F) and (H). It is prepared as a two-pack type in which these are mixed at the time of use. The component (H) may be mixed with the component (E) and the component (G) instead of the component (F).

When the composition of the present invention is used, a suitable organic solvent such as toluene, depending on the use and purpose,
It may be used after being dispersed or dissolved in xylene or the like.

As a method for evaluating the adhesiveness between the polybutylene terephthalate resin composition and the addition-cured silicone rubber, a molded product of the polybutylene terephthalate composition is molded in advance, and the molded product is subjected to the liquid addition-curing described above. Of the polybutylene terephthalate resin composition by applying a type silicone rubber and curing at room temperature for 24 to 48 hours and at 80 to 200 ° C. for 60 to 4 hours. It is possible to obtain good adhesiveness with the molded product.

[0055]

EXAMPLES The present invention will be specifically described below with reference to examples.

In the examples, "parts" means "parts by weight". The intrinsic viscosity [η] of the polymer is 3 in orthochlorophenol.
It is a value calculated from the solution viscosity measured at 5 ° C.

The terminal carboxyl group concentration (COO
H) is the method of A. Conix {(Makromol. Chem, Vol- 26 , 22.
6 (1958)} per 10 ⁶ g of polymer.

Examples 1 to 3, Comparative Examples 1 to 7 Polybutylene terephthalate (intrinsic viscosity: 0.90) using tetrabutoxide titanate was used as a polymerization catalyst.
After drying at 5 ° C for 5 hours, methylhydrogen silicone oil (manufactured by Toray Dow: trade name SH1107) is used as a silicon-containing compound, and pentaerythrityl-tetrakis [3- (3,5-di-t] is used as a phenolic antioxidant. -
Butyl-4-hydroxyphenyl) propionate],
Tetrakis [methylene-
3- (dodecylthio) propionate] was uniformly mixed in a V-blender at various ratios shown in Table 1. The obtained mixture was heated at a barrel temperature of 250 with a twin-screw extruder having a diameter of 44 mm.
The thread discharged from the die was cooled and cut by melting and kneading at 0 ° C. to obtain a molding pellet.

Next, after drying the pellets at 130 ° C. for 5 hours, a test piece mold for physical properties was attached to a 5 ounce injection molding machine, the cylinder temperature was 260 ° C., and the mold temperature was 4 °.
Tensile test pieces (AS) under the molding conditions of 0 ° C., injection pressure 700 kg / cm ² , cooling time 20 seconds, and total cycle 35 seconds.
TM4) and an adhesion test piece were molded. The hydrolysis resistance test was carried out by measuring the tensile strength and the elongation at break of a test piece which had been subjected to a wet heat treatment for 60 hours at 122 ° C. and a humidity of 100%. Temperature 1 for heat resistance test
It was carried out by measuring the tensile strength and the breaking elongation of a test piece which was heat-treated at 70 ° C. for 500 hours.

Preparation of Addition Type Silicone Rubber: As component (A), dimethylpolysiloxane having two methylvinylsiloxane units in one molecule and terminated with a dimethylvinylsiloxy group (viscosity at 25 ° C .: 1000 cSt. ) 100 parts by weight, hydrogen atom bonded to silicon atom as the component (B) is 0.73 per 100 g.
3. Methyl hydrmediene polysiloxane having 9 moles.
6 parts by weight, 0.12 parts by weight of an octyl alcohol modified solution of chloroplatinic acid as the component (C) (platinum content: 0.5%), a reaction inhibitor as the component (D), represented by the following formula:

[0061]

Embedded image

Polymer represented by (manufactured by a conventionally known method, appearance: unemployed transparent, at 25 ° C .: 13 cS
t) 0.5 part by weight was prepared.

The adhesion test between the above polybutylene terephthalate resin composition and the addition-curable silicone rubber is shown in FIG.
The adhesive test piece shown in Fig. 1 is applied under the conditions of width 25 mm, length 15 mm, and thickness 0.2 mm, and is cured by heating at 130 ° C. for 1 minute to obtain the adhesive strength between the polybutylene terephthalate resin composition and the silicone rubber, and the silicone. The peelability between the rubber and chrome-plated adhesion test piece and a metal jig of the same size was evaluated.

The results obtained are shown in Table 1.

[0065]

[Table 1]

As shown in Table 1, the polybutylene terephthalate resin having a terminal carboxyl group concentration of 35 equivalents / 10 ⁶ g was inferior in hydrolysis resistance as shown by the PCT results.
On the other hand, it is understood that the polybutylene terephthalate resin having a terminal carboxyl group concentration of 10 equivalents / 10 ⁶ g shows good results.

The heat aging property is greatly improved by combining a phenol type antioxidant and a thioether type antioxidant.

Further, by adding methylhydrogen silicone oil to the polybutylene terephthalate resin composition and adding an adhesiveness-imparting component (H) component to the addition-curable silicone rubber, the polybutylene terephthalate resin becomes a silicone rubber. It is possible to obtain a result in which the adhesiveness is strong and the peelability from the metal is good.

[Example 4, Comparative Examples 8 to 9] By the same method as in Example 1, the same evaluation was performed on the compositions having the blending ratios shown in Table 2.

As a result, it was found that when a polybutylene terephthalate resin using a tin compound as a catalyst and a phosphorus antioxidant were added, the silicone rubber did not cure and could not be used.

[0071]

[Table 2]

[Brief description of the drawings]

FIG. 1 is an elevational view showing a state in which an addition-curable silicone rubber is coated on the surface of a molded product made of the polybutylene terephthalate resin composition of the present invention and sandwiched between the molded product made of metal (chrome plated sheet). is there.

FIG. 2 is a plan view showing the plane of FIG. 1;

[Explanation of symbols]

10 is a coating layer of silicone rubber. 12 is a polybutylene terephthalate molded product. Reference numeral 14 is a chrome-plated metal plate (metal plate).

Continuation of front page (51) Int.Cl. ⁶ Identification number Office reference number FI Technical display area C08K 5/54 C08K 5/54 C08L 67/02 C08L 67/02 KKE KKE C09D 183/07 PMV C09D 183/07 PMV // C08L 83:05

Claims (1)

[Claims] 1. (B) Per 100 parts by weight of polybutylene terephthalate having a terminal carboxyl concentration of 15 equivalents / ton or less and a titanium compound as a polymerization catalyst, (B)
A silicon compound and / or a polymer thereof having a hydrogen atom directly bonded to at least one silicon atom in one molecule is prepared as follows.
05 to 3 parts by weight, (C) phenolic antioxidant 0.01
.About.0.5 part by weight and (D) a thioether antioxidant.
A molded product obtained by molding a polybutylene terephthalate resin composition prepared by blending 01 to 0.5 parts by weight is added to a (E) molecule as an addition-curable silicone rubber, and at least a vinyl group bonded to a silicon atom is contained in the molecule. Organopolysiloxane having two, (F) an organohydrogenpolysiloxane having at least two hydrogen atoms bonded to silicon atoms in one molecule, (G) a platinum compound, and (H) the following general formula (1) 1] (In the formula, R ¹ is a substituted or unsubstituted monovalent hydrocarbon group containing no aliphatic unsaturated bond, and when plural R ¹ are present, they may be different. K is 0 or Which is an integer of 1 or more) and a coating liquid comprising an organopolysiloxane composition containing a terminal trivinylsilyl-terminated organopolysiloxane, which is applied and cured to form an integral body of a thermoplastic polyester and a silicone rubber. Molded body.