JP2001329165A - Reinforced polyamide resin composition excellent in solvent welding strength - Google Patents

Abstract

PROBLEM TO BE SOLVED: To obtain a reinforced polyamide resin composition excellent in flowability and cyclicity in molding and producing a molded article having a high solvent welding strength in various welding methods. SOLUTION: This reinforced polyamide resin composition for molding producing a molded article excellent in the strength of solvent-welded parts comprises (A) 96-99.9 wt.% of a crystalline polyamide resin and (B) 0.1-4 wt.% of a partially amorphous copolyamide comprising at least two aromatic monomer components, and (C) 5-200 pts.wt of an inorganic filler per 100 pts.wt of the polyamide resin.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a reinforced polyamide resin composition having excellent mechanical properties and moldability and having excellent welding strength. These resin compositions are used as materials for automobiles and electric and electronic parts.

[0002]

2. Description of the Related Art Crystalline polyamide resins are widely used as industrial materials because of their high strength and rigidity.
However, reinforced polyamides that use only crystalline polyamides as the polyamides have a high welding strength due to their crystallinity.In recent years, when welding, which has become widely used when manufacturing resin parts, is performed, the strength of the portions is not sufficient. Can not be used for parts that require, and when using a polyamide consisting of amorphous polyamide only, the vibration welding strength is sufficient, but because of poor moldability, especially fluidity, the injection welding strength is low. This has also been restricted in use.

[0003] With respect to techniques for improving the welding strength of crystalline polyamide, various studies have been made with the increase in the number of parts using welding in recent years. JP-A-9-17648
No. 4, JP-A-10-219106 proposes a method for improving the weldability of nylon using copper iodide and potassium iodide. However, this method has problems such as a decrease in mechanical strength and generation of a decomposition gas at the time of molding due to a large amount of potassium iodide and copper iodide actually used. JP-A-8-3377
No. 18 proposes a method using crystalline copolymerized nylon, but when copolymerized nylon is used, the weldability is significantly improved, but the mechanical strength and rigidity are reduced and heat resistance is reduced. The use is limited because the durability decreases.

[0004] Compositions similar to the composition of the present invention have been known for a long time, and are described in JP-A-58-53949 and JP-A-58-53949.
The technology is disclosed in JP-A-8-53950. However, since these inventions are techniques for improving the metal halide resistance and hot water resistance of aliphatic nylon, and the low warpage, the amount of amorphous nylon is required to be larger than that of the present invention. It is not known at all that the effect of improving the weldability can be obtained within the composition range of the present invention.

[0005]

DISCLOSURE OF THE INVENTION In order to solve the above-mentioned problems, the present invention provides a reinforced polyamide resin composition which is excellent in fluidity and high cycle property at the time of molding and has high strength by various welding methods. It is to provide.

[0006]

Means for Solving the Problems The inventors of the present invention have conducted intensive studies to solve this problem, and as a result, have found that a crystalline polyamide has an amorphous partially aromatic copolymer containing at least two aromatic monomer components at least. The present inventors have found that the object can be achieved by adding a polymerized polyamide resin, and have reached the present invention.

That is, the present invention relates to (A) 96 to 99.9% by weight of a crystalline polyamide resin and (B) 0.1 to 4% of an amorphous partially aromatic copolymerized polyamide resin containing at least two aromatic monomer components. The present invention relates to a reinforced polyamide resin composition for molding excellent in the strength of a welded portion, which is (C) 5 to 200 parts by weight of an inorganic filler with respect to 100 parts by weight of a polyamide resin consisting of 100% by weight.

[0008]

DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be described below in detail.
The (A) crystalline polyamide resin used in the present invention comprises an aliphatic diamine and an aliphatic dicarboxylic acid,
Or an aliphatic polyamide resin comprising lactam or aminocarboxylic acid or a partially aromatic copolymerized polyamide resin containing one aromatic monomer component.

The monomer components of the aliphatic polyamide resin include an aliphatic diamine having 4 to 12 carbon atoms and an aliphatic diamine having 6 to 1 carbon atoms.
2 aliphatic dicarboxylic acids, lactams having 6 to 12 carbon atoms, or aminocarboxylic acids having 6 to 12 carbon atoms. Specific examples of the aliphatic diamine include tetramethylene diamine, hexamethylene diamine, octamethylene diamine, nonamethylene diamine, undecamethylene diamine, dodecamethylene diamine, and the like. Specific examples of the aliphatic dicarboxylic acid include adipic acid, heptanedicarboxylic acid, octanedicarboxylic acid, nonanedicarboxylic acid, undecanedicarboxylic acid, dodecanedicarboxylic acid, and the like. A preferred combination of aliphatic diamine and aliphatic dicarboxylic acid is an equimolar salt of hexamethylene diamine and adipic acid. Specific examples of lactams include α-pyrrolidone, ε-caprolactam, ω-laurolactam,
Specific examples of aminocaproic acid include 6-aminocaproic acid, 7-aminoheptanoic acid, 11-aminoundecanoic acid, 12-aminododecanoic acid, etc., and 6-aminocaproic acid,
Preferred are 12-aminododecanoic acid, ε-caprolactam and laurolactam. The aliphatic polyamide-forming monomer may be used alone or as a mixture of two or more components.

Specific examples of the aliphatic polyamide resin formed from these monomer components include nylon 6, nylon 11, nylon 12, nylon 66 and nylon 61.
0, nylon 612, and nylon 116, which may be homopolymers or copolymers of two or more.

The crystalline partially aromatic copolymerized polyamide resin containing one aromatic monomer component includes terephthalic acid,
It is a copolymer polyamide containing one aromatic monomer component such as an aromatic dicarboxylic acid component such as isophthalic acid and naphthalenedicarboxylic acid. Preferably, it is a crystalline partially aromatic copolymerized polyamide resin containing one aromatic monomer component and having a melting point of 260 ° C. or more and less than 320 ° C., and more preferably contains one aromatic monomer component and has a melting point. It is a crystalline partially aromatic copolymerized polyamide resin having a temperature of 290 ° C. or more and less than 316 ° C. Preferred combinations of the crystalline partially aromatic copolymerized polyamide resin containing one aromatic monomer component include an equimolar salt of an aliphatic diamine and an aliphatic dicarboxylic acid, an equimolar salt of an aliphatic diamine and an aromatic dicarboxylic acid, and And / or a crystalline copolymerized polyamide comprising an aliphatic polyamide-forming monomer.

Here, the aliphatic diamine is one having 4 to 12 carbon atoms.
And aliphatic methylene diamines such as tetramethylene diamine, hexamethylene diamine, octamethylene diamine, nonamethylenediamine, undecamethylene diamine, and dodecamethylene diamine. Aliphatic dicarboxylic acids are aliphatic dicarboxylic acids having 6 to 12 carbon atoms, and include adipic acid, heptanedicarboxylic acid, octanedicarboxylic acid, nonanedicarboxylic acid, undecanedicarboxylic acid, dodecanedicarboxylic acid, and the like. A preferred combination is an equimolar salt of hexamethylenediamine and adipic acid.

The aromatic dicarboxylic acid includes terephthalic acid, isophthalic acid, naphthalenedicarboxylic acid and the like, and a preferred combination is an equimolar salt of hexamethylenediamine and terephthalic acid.

As the aliphatic-forming monomer, a compound having 6 to 6 carbon atoms is used.
12 aminocarboxylic acids and lactams having 6 to 12 carbon atoms, 6-aminocaproic acid, 7-aminoheptanoic acid, 11-aminoundecanoic acid, 12-aminododecanoic acid, α-pyrrolidone, ε-caprolactam, laurolactam , Ε-enantholactam and the like,
Aminocaproic acid, 12-aminododecanoic acid, ε-caprolactam and laurolactam are preferred. The aliphatic polyamide-forming monomer may be used alone or as a mixture of two or more components.

The amounts used are 30 to 70% by weight of an equimolar salt of hexamethylenediamine and adipic acid, 70 to 30% by weight of an equimolar salt of hexamethylenediamine and terephthalic acid, and 0 to 15% by weight of an aliphatic polyamide-forming monomer. %, Preferably 35 to 55% by weight of an equimolar salt of hexamethylenediamine and adipic acid, 65 to 45% by weight of an equimolar salt of hexamethylenediamine and terephthalic acid, and 0 to 10% by weight of an aliphatic polyamide-forming monomer. is there.

Although the degree of polymerization of the crystalline polyamide resin in the present invention is not particularly limited, 1 g of the polymer is dissolved in 100 ml of 96% concentrated sulfuric acid, and the relative viscosity measured at 25 ° C. is 1.8 to 5.0. It is more preferably, and more preferably 2.0 to 3.0. When the relative viscosity is higher than the upper limit of the above numerical value, the workability is significantly impaired, and when the relative viscosity is lower than the above lower limit, the mechanical strength decreases, which is not preferable.

The (B) amorphous partially aromatic copolymerized polyamide resin containing at least two aromatic monomer components used in the present invention contains at least one terephthalic acid component or a heteroaromatic compound in addition to isophthalic acid. It is a polyamide resin. This amorphous partially aromatic copolymerized polyamide resin is an amorphous polyamide having a glass transition temperature of 100 ° C. or higher determined by the peak temperature of the loss modulus at the time of absolute drying obtained by the measurement of dynamic viscoelasticity. Preferably, two or more sets containing an equimolar salt of an aliphatic diamine and an aromatic dicarboxylic acid are desirable.

Here, the aliphatic diamine has 4 to 12 carbon atoms.
And aliphatic methylene diamines such as tetramethylene diamine, hexamethylene diamine, octamethylene diamine, nonamethylene diamine, undecamethylene diamine, and dodecamethylene diamine.

Examples of the aromatic dicarboxylic acid include terephthalic acid, isophthalic acid, naphthalenedicarboxylic acid and the like. A preferred combination is an equimolar salt of hexamethylenediamine and terephthalic acid and an equimolar salt of hexamethylenediamine and isophthalic acid. is there.

The amorphous partially aromatic copolymerized polyamide resin (B) containing at least two aromatic monomer components used in the present invention includes a polyamide-forming component 10 composed of an aliphatic diamine, isophthalic acid and terephthalic acid.
0-60% by weight and aliphatic polyamide component 0-40% by weight
Is preferred. The equimolar salt of an aliphatic diamine and an aromatic dicarboxylic acid includes 60 to 95 mol% of a terephthalic acid component unit and 5 to 4 mol of an isophthalic acid component unit.
Those comprising 0 mol% and an aliphatic diamine are preferred.

In the present invention, the mixing ratio of (A) the crystalline polyamide resin and (B) the amorphous partially aromatic copolymerized polyamide resin containing at least two aromatic monomer components is such that (A) the resin is 96-99. 9.9% by weight, and (B) resin in the range of 0.1 to 4% by weight. Preferably, (A) the resin is 97 to 99% by weight, and (B) the resin is 1 to 3% by weight.

When the amount of the amorphous partially aromatic copolymerized polyamide resin (B) is more than the above upper limit, the fluidity in the mold is deteriorated, and the crystallization is delayed to deteriorate the high cycle moldability. Not preferred.

On the other hand, if the amount of the amorphous partially aromatic polyamide resin (B) used is less than the lower limit of the above value, the effect of improving the welding strength is small and the object of the present invention cannot be achieved.

The (C) inorganic filler used in the present invention comprises:
Fibrous inorganic materials such as glass fiber and carbon fiber, wollastonite and potassium titanate whisker, montmorillonite, talc, mica, calcium carbonate, silica, clay, kaolin, glass powder, glass beads, and other inorganic fillers, various organic or An organic filler such as a polymer powder may be used, but glass fiber or talc is preferably used, and glass fiber is more preferable. The fibrous filler has a fiber diameter of 0.01 to 20 μm, preferably 0.03 to 15 μm, and a fiber cut length of 0.5 to 0.5 μm.
10 to 10 mm, preferably 0.7 to 5 mm.

The amount of the inorganic filler (C) used in the present invention is based on 100 parts by weight of the obtained polyamide resin.
The amount is 5 to 200 parts by weight, preferably 10 to 150 parts by weight, more preferably 10 to 100 parts by weight. If the amount is less than 5 parts by weight, the mechanical strength of the polyamide resin is not sufficiently satisfied. If the amount is more than 200 parts by weight, the mechanical strength is sufficiently satisfied, but the moldability and the surface condition deteriorate, which is not preferable.

The resin composition of the present invention can be used as it is as a material for automobiles or electric / electronic parts, but as long as its purpose is not impaired, a heat-resistant agent, a weather-resistant agent, a crystal nucleating agent, a crystallization accelerator, Functionality-imparting agents such as a mold agent, a lubricant, an antistatic agent, a flame retardant, a flame retardant auxiliary, and a coloring agent can be used.

More specifically, hindered phenols, phosphites, thioethers,
Copper halogenated and the like can be mentioned, and these can be used alone or in combination. Examples of the weathering agent include hindered amines and salicylates, which can be used alone or in combination. As a crystal nucleating agent, talc,
Examples include inorganic fillers such as clay and organic crystal nucleating agents such as fatty acid metal salts, and these can be used alone or in combination. Examples of the crystallization promoter include low molecular weight polyamides, higher fatty acids, higher fatty acid esters and higher fatty alcohols, and these can be used alone or in combination. Release agents include fatty acid metal salts,
Examples thereof include fatty acid amides and various waxes, which can be used alone or in combination. Examples of the antistatic agent include aliphatic alcohols, aliphatic alcohol esters and higher fatty acid esters, and these can be used alone or in combination. Flame retardants include metal hydroxides such as magnesium hydroxide, phosphorus, ammonium phosphate, ammonium polyphosphate, melamine cyanurate,
Ethylene dimelamine dicyanurate, potassium nitrate, brominated epoxy compound, brominated polycarbonate compound,
Brominated polystyrene compounds, tetrabromobenzyl polyacrylate, polycondensates of tribromophenol, polybromobiphenyl ethers and chlorine-based flame retardants,
They can be used alone or in combination.

Other thermoplastic resin compositions can be added to the resin composition of the present invention as long as the object of the present invention is not impaired. Examples of the thermoplastic resin used in combination are polyethylene, polypropylene, polystyrene, ABS resin, A
General-purpose resin materials such as S resin and acrylic resin, nylon 6,
Examples thereof include aliphatic polyamide resins such as nylon 66 and nylon 12, polycarbonate, polyphenylene oxide, polyethylene terephthalate, polybutylene terephthalate, polyphenylene sulfide, and other high heat resistant resins. In particular, when polyethylene or polypropylene is used in combination, it is desirable to use those modified with maleic anhydride, a glycidyl group-containing monomer, or the like.

The resin composition of the present invention may be formed by blending respective resin pellets and melt-mixing at the stage of obtaining a final product, or may be previously melted by a single-screw or twin-screw extruder, a Banbury mixer or the like. After mixing, the mixture can be subjected to molding. Thus, it can be used for extrusion molding, blow molding or injection molding.

When the composition of the present invention is used for a product using a welding method, its performance can be remarkably exhibited, but is not limited thereto. Specific examples of the welding method include a vibration welding method, an injection welding method such as die slide injection (DSI) and a die rotary injection (DRI), an ultrasonic welding method, a spin welding method, a hot plate welding method, a hot wire welding method, and a laser welding method. And a high-frequency induction heating welding method.

Further, the composition of the present invention exhibits its performance even in products having a melt-bonded portion such as a multicolored molding or a weld portion.

The composition of the present invention can be used for engines of automobiles and motorcycles, transmissions, differential mechanism parts, chassis parts, exterior parts, interior parts and electric parts,
Can be used for electric and electronic parts. Specific examples include oil strainers, timing chain covers, rocker covers, intake manifolds, fuel rails,
Timing chain tensioner, thrust washer, power steering tank, brake fluid sub tank, canister, automatic transmission stator, air cleaner, resonator, vacuum tank, throttle body, radiator tank, thermostat housing, radiator inlet pipe, radiator outlet pipe, gear, retainer, Mechanical parts such as front end, headlight stay, lower arm, link, etc., hollow parts such as air duct, gasoline tank, brake pipe, fuel pipe, etc.
Examples include pedals such as an accelerator pedal, a brake pedal, and a clutch pedal, electric components such as a sensor, a relay box, and a connector, and electric and electronic components such as a terminal block, a connector, and a relay.

(Examples) The present invention will be specifically described below with reference to Examples and Comparative Examples, but the present invention is not limited thereto. The measurement of the physical properties of the molded articles in Examples and Comparative Examples was performed as follows.

(Evaluation of Physical Properties) (Evaluation of Mechanical Properties) Evaluation was performed under the following conditions. All evaluations were performed in a dry state. (1) Tensile strength and elongation: According to ASTM D638, a 3.2 mm-thick No. 1 test piece was used at a pulling rate of 5 mm / min. (2) Flexural strength and flexural modulus: According to ASTM D790, a three-point bending test was performed using a 3.2 mm-thick strip-shaped test piece. (3) Impact strength: According to ASTM D256, a 3.2 mm-thick strip-shaped test piece was notched by post-processing and evaluated by an Izod impact test apparatus.

(Evaluation of Formability) (4) Flow Length: Using a spiral mold for measuring the flow length of a rod having a width of 12.5 mm and a thickness of 1 mm, the flow length at an injection pressure of 50 MPa was measured with an SG75 injection molding machine manufactured by Sumitomo Heavy Industries. did.

(Evaluation of Welding Strength) (5) Injection Welding Strength: Tension of a test piece having the shape shown in FIGS. 1 to 3 formed by the DRI method using the composition obtained in the present invention under the following conditions. The strength was measured. The tensile conditions were a tensile speed of 5 mm / sec and a distance between chucks of 25 mm. Molding machine: Nikko N140BII Resin temperature: See Tables 1 and 2. Mold temperature: 80 ° C Holding pressure: 20 MPa Injection time: 1 sec Cooling time: 20 sec

Example 1 97% by weight of polyamide 6 (1015B manufactured by Ube Industries, Ltd .; relative viscosity 2.65) and 3% by weight of polyamide 6I / 6T (Grivory G21 manufactured by EMS) were previously mixed uniformly and then barreled. 44mmφ set at a temperature of 270 ° C
The mixture was kneaded with a twin-screw extruder equipped with a vent. When kneading the polyamide resin, glass fiber (manufactured by Nippon Electric Glass Co., Ltd., glass fiber diameter: 11 μm, glass fiber cut length: 3 mm) is supplied from the middle of the extruder so as to be 45 parts by weight with respect to 100 parts by weight of the polyamide resin. Then, an intended reinforced polyamide resin composition pellet was prepared. Next, the obtained pellet is
After drying under reduced pressure of 10 ° C. and 10 torr for 24 hours, injection molding was performed at a cylinder temperature of 270 ° C. and a mold temperature of 80 ° C.
The molding and flowability of a tensile test piece, a bending test piece, and an impact test piece based on STM were evaluated. Further, the tensile strength of the test piece formed by the DRI method was measured. Table 1 shows the obtained results.
It was shown to.

Examples 2 to 5 Table 1 shows the charging ratio of polyamide 6 and polyamide 6I / 6T.
A reinforced polyamide resin composition was prepared in the same manner as in Example 1 except that the properties were changed as shown in Table 1, and the physical properties thereof were evaluated. The results obtained are shown in Table 1.

Examples 6 and 7 A reinforced polyamide resin composition was prepared in the same manner as in Example 1 except that the proportion of the glass fibers was changed as shown in Table 1.
The physical properties were evaluated. The results obtained are shown in Table 1.

Example 8 A reinforced polyamide resin composition was prepared in the same manner as in Example 1 except that talc (talc cup manufactured by Tsuchiya Kaolin Kogyo KK) was supplied in a proportion of 45 parts by weight instead of glass fiber. Physical properties were evaluated. The results obtained are shown in Table 1.

Comparative Example 1 A reinforced polyamide resin was prepared according to Example 1 without using the amorphous partially aromatic copolymerized polyamide resin of (B), and the physical properties thereof were evaluated. The obtained results are also shown in Table 1.

Comparative Examples 2-3 Table 1 shows the proportions of polyamide 6 and polyamide 6I / 6T charged.
A reinforced polyamide resin composition was prepared in the same manner as in Example 1 except that the properties were changed as shown in Table 1, and the physical properties thereof were evaluated. The results obtained are shown in Table 1.

Example 9 A reinforced polyamide resin was prepared in the same manner as in Example 1 except that polyamide 66 (2020B manufactured by Ube Industries, Ltd .; relative viscosity 2.70) was used as the polyamide resin, and its physical properties were evaluated. Kneading was performed at a barrel temperature of 285 ° C., and injection molding was performed at a cylinder temperature of 275 ° C. and a mold temperature of 80 ° C. The results obtained are shown in Table 2.

Example 10 As a polyamide resin, polyamide 66 / 6T (Ube Industries, Ltd.)
A reinforced polyamide resin composition was prepared in the same manner as in Example 1 except that 8123X (manufactured by Corporation; relative viscosity 2.30) was used.
The physical properties were evaluated. The kneading was performed at a barrel temperature of 320 ° C., and injection molding was performed at a cylinder temperature of 320 ° C. and a mold temperature of 110 ° C. The obtained results are shown in Table 2.

Example 11 Polyamide 6/66 (Ube Industries, Ltd.) as a polyamide resin
A reinforced polyamide resin composition was prepared in the same manner as in Example 1 except that 2123B manufactured by Co., Ltd .; and the relative viscosity was 2.65, and the physical properties were evaluated. The kneading was performed at a barrel temperature of 280 ° C., and injection molding was performed at a cylinder temperature of 270 ° C. and a mold temperature of 80 ° C. The obtained results are also shown in Table 2.

Example 12 A reinforced polyamide resin composition was prepared in the same manner as in Example 1 except that polyamide 12 (3020B, manufactured by Ube Industries, Ltd .; relative viscosity: 2.90) was used as the polyamide resin, and its physical properties were evaluated. did. The kneading was performed at a barrel temperature of 240 ° C., and injection molding was performed at a cylinder temperature of 240 ° C. and a mold temperature of 80 ° C. The obtained results are also shown in Table 2.

Example 13 Polyamide 6 having a relative viscosity of 2.45 as a polyamide resin
Example 1 except that (1013B manufactured by Ube Industries, Ltd.) was used.
A reinforced polyamide resin was prepared in the same manner as described above, and its physical properties were evaluated. The obtained results are also shown in Table 2.

Example 14 Polyamide resin having a relative viscosity of 2.90 polyamide 6
Example 1 except that (Ube Industries, Ltd. 1022B) was used.
A reinforced polyamide resin was prepared in the same manner as described above, and its physical properties were evaluated. The obtained results are also shown in Table 2.

Example 15 Polyamide resin having a relative viscosity of 3.20 polyamide 6
Example 1 except that (1030B manufactured by Ube Industries, Ltd.) was used.
A reinforced polyamide resin was prepared in the same manner as described above, and its physical properties were evaluated. The obtained results are also shown in Table 2.

Comparative Example 4 A reinforced polyamide resin was prepared according to Example 9 without using the amorphous partially aromatic copolymerized polyamide resin of (B), and the physical properties thereof were evaluated. The obtained results are also shown in Table 2.

Comparative Example 5 A reinforced polyamide resin was prepared according to Example 10 without using the amorphous partially aromatic copolymerized polyamide resin of (B).
The physical properties were evaluated. The obtained results are also shown in Table 2.

[0052]

[Table 1]

[0053]

[Table 2]

From these results, when the ratio of the resin (B) is reduced, the effect of improving the welding strength is not exhibited. Conversely, when the ratio of the resin (B) is increased, the fluidity in the mold is reduced and the moldability is reduced. Worsens. The effect of the resin (B) is effective for various crystalline polyamide resins.

[0055]

The reinforced polyamide resin composition of the present invention comprises:
It has high welding strength without damaging the intrinsic mechanical properties of the crystalline polyamide resin. For this reason, it can be used for a large molded product or a component having a complicated shape without depending on a special molding machine or a post-processing method.

[Brief description of the drawings]

FIG. 1 shows a front view of an example of a test piece.
(The unit of the numerical value is mm)

FIG. 2 shows a side view of an example of a test piece.
(The unit of the numerical value is mm)

FIG. 3 shows a state diagram of a test piece formed by the DRI method.

 ──────────────────────────────────────────────────続 き Continued on the front page F term (reference) 4J002 CL011 CL031 CL032 CL051 DA016 DE186 DE236 DJ006 DJ016 DJ036 DJ046 DJ056 DL006 FA046 FD016 FD060 FD080 FD100 FD130 FD160 GN00 GQ00

Claims (6)

[Claims] (A) a crystalline polyamide resin of 96 to 99.
9% by weight (B) 100 parts by weight of a polyamide resin comprising 0.1 to 4% by weight of an amorphous partially aromatic copolymerized polyamide resin containing at least two aromatic monomer components, and (C) an inorganic filler 5 to 5% by weight. A reinforced polyamide resin composition for molding excellent in the strength of a welded portion of 200 parts by weight. 2. The reinforced polyamide resin composition for molding according to claim 1, wherein the crystalline polyamide resin comprises an aliphatic diamine and an aliphatic dibasic acid or a lactam. 3. The reinforced polyamide resin composition for molding according to claim 1, wherein the crystalline polyamide resin comprises terephthalic acid or an inducer thereof and an aliphatic diamine. 4. An amorphous partially aromatic copolymerized polyamide resin containing at least two aromatic monomer components, comprising 60 to 95 mol% of a terephthalic acid component unit, 5 to 40 mol% of an isophthalic acid component unit, and an aliphatic diamine. The reinforced polyamide resin composition for molding according to claim 1, which is excellent in the strength of the welded portion. 5. An amorphous partially aromatic copolymerized polyamide resin containing at least two aromatic monomer components, wherein said polyamide-forming component is composed of an aliphatic diamine, isophthalic acid and terephthalic acid in an amount of from 100 to 60% by weight and an aliphatic polyamide. The reinforced polyamide resin composition for molding according to claim 1, wherein the component is 0 to 40% by weight. 6. The reinforced polyamide resin composition for molding according to claim 1, wherein the inorganic filler is glass fiber.