JP5959183B2 - Resin composition - Google Patents

Description

  The present invention relates to a resin composition suitable as a manufacturing material for a thin molded product for use in a housing or an internal chassis of an electronic device such as a mobile phone, a thin molded product using the resin composition, and a manufacturing method thereof.

  Electronic device housings such as mobile phones are made of thin molded bodies, which require high flexural modulus, excellent impact resistance, small dimensional change due to water absorption, and in some cases flame resistance. The

Patent Document 1 describes a lightweight resin composition for an automobile engine room made of a glass fiber-containing thermoplastic resin and manufacturing a molded product by applying injection compression molding from the composition.
Although many types of thermoplastic resins are listed in paragraph 0031, there is no description about blending a flame retardant and imparting flame retardancy when improving flame retardancy.
Paragraph No. 0042 describes that the average glass fiber length in the molded product is in the range of 2 to 20 mm, particularly 3 to 15 mm, and the total length is 3 to 100 mm, preferably 4 to 50 mm, so as to be within the above range. It is described that glass fiber reinforced thermoplastic resin pellets in which glass fibers are arranged in parallel to each other can be used.

Patent Document 2 includes an inorganic fiber having a length of 3 to 100 mm, including a thermoplastic resin having a bending elastic modulus in a predetermined range and 10 to 90% by weight of inorganic fibers arranged in parallel to each other and having almost the same length of pellets. The invention of the containing thermoplastic resin pellet is described.
Paragraph No. 0041 lists a number of optional components, which include flame retardants and flame retardant aids, but are not used in the examples, especially for imparting flame retardancy. Not listed.
Paragraph No. 0055 describes that it is expected to be used as an energy and resource saving material in various fields such as automobile interior materials, building materials, and civil engineering.

Patent Document 3 describes a composition obtained by dry-mixing (A) long fiber reinforced thermoplastic resin pellets, (B) flame retardant pellets, and (C) a lubricant.
A large number of thermoplastic resins and long fibers that can be used as the component (A) are listed in paragraphs 0025 and 0041, but there is no description of combinations of specific resins and long fibers.
Paragraph number 0095 describes uses of casings, housings, and the like of electronic devices.

  Patent Document 4 discloses a flame retardant glass fiber reinforced resin composition containing a glass fiber chopped strand using an epoxy sizing agent and an organic halogen-containing flame retardant as a flame retardant.

Patent Document 5, a polycarbonate resin, styrene resin, that the long fiber-reinforced thermoplastic resin composition comprising reinforcing fibers have been disclosed. Moreover, when improving a flame retardance, there is no description about mix | blending a flame retardant and providing a flame retardance .

JP 2000-257442 A JP 2000-289023 A JP 2009-167270 A JP 7-11100 A JP 2008-202012 A

  An object of the present invention is to provide a resin composition from which a thin molded article having excellent mechanical strength and heat resistance can be obtained.

  Another object of the present invention is to provide a thin-walled molded article having excellent mechanical strength and heat resistance and a method for producing the same.

As a means for solving the problems, the present invention
(A) A thermoplastic resin containing a polycarbonate-based resin, (B) a fluidity improver, and optionally (C) a flame retardant, and (D) a resin-attached long fiber bundle containing reinforcing long fibers A composition comprising:
The resin-attached long fiber bundle is bundled in a state where the reinforcing long fibers of the component (D) are aligned in the length direction, and the bundle of reinforcing long fibers (A) and (B), and further if necessary Then, after the components including the component (C) are adhered and integrated in a melted state, a resin composition is provided which is cut to a length of 3 to 30 mm.

  As a means for solving other problems, the present invention is a thin molded article comprising the above resin composition and having a thickness of 0.3 to 1.5 mm and a remaining fiber length of 0.3 to 1.5 mm. I will provide a.

The present invention is a method for producing a thin-walled molded article using the above resin composition as a means for solving another problem,
Provided is a method for producing a thin molded article, wherein the resin composition is molded by an injection molding method or an injection compression molding method.

  The molded product obtained from the resin composition of the present invention has high mechanical strength and heat resistance even if it is thin, and when it is made into a composition containing a flame retardant, the mechanical strength described above, Flame retardancy can be imparted while maintaining the heat resistance at a high level. For this reason, it is suitable for various thin-walled molded product applications that require mechanical strength, heat resistance, and, if necessary, flame retardancy.

<Resin composition>
The composition of the present invention comprises a resin-attached continuous fiber bundle containing the component (A), the component (B) and, if necessary, the component (C), and further containing the component (D). It may be composed of only, or may further contain other components as necessary.

  The resin-attached fiber bundle contained in the composition of the present invention is composed of (A) component and (B) component in the reinforcing long fiber bundle in which the reinforcing long fibers for component (D) are bundled in the length direction. If necessary, the component containing the component (C) is adhered and integrated in a melted state, and then cut to a length of 3 to 30 mm.

Resin-attached fiber bundles contained in the composition of the present invention are (A) and (B) components attached to reinforcing long fiber bundles, and if necessary, (C) components are attached.
The resin is infiltrated (impregnated) to the center of the reinforcing long fiber bundle, and the resin has entered between the fibers in the center of the fiber bundle (hereinafter referred to as “resin-impregnated fiber bundle”),
A state in which only the surface of the reinforcing long fiber bundle is covered with resin (hereinafter referred to as “resin surface coated fiber bundle”),
In the middle of them (the fiber bundle surface is covered with resin, the resin is impregnated only in the vicinity of the surface, and the resin does not enter the center) (hereinafter referred to as “partially impregnated fiber bundle”) It is a waste.

  The resin-attached fiber bundle contained in the composition of the present invention is preferably a resin-impregnated fiber bundle from the viewpoint of dispersibility and fluidity.

[Component (A)]
(A) The thermoplastic resin of a component contains a polycarbonate-type resin.
The component (A) thermoplastic resin preferably contains (A-2) a styrene resin and / or a polyester resin in addition to the (A-1) polycarbonate resin.

As the polycarbonate-based resin of the component (A-1), 2,2-bis (4-oxyphenyl) alkane-based, bis (4-oxyphenyl) ether-based, bis (4-oxyphenyl) sulfone, sulfide or In addition to polymers or copolymers [component (A-1-1)] consisting of bisphenols such as sulfoxides, copolymers [(A-1-2)] of polycarbonate and organosiloxane Can be mentioned.
As the (A-1) component polycarbonate resin, the component (A-1-1) or the component (A-1-2) is used alone, the component (A-1-1) and the component (A-1 -2) Components can be used in combination.

  As the polycarbonate-based resin of component (A-1-1), known resins can be used, for example, those described in paragraph Nos. 0010 and 0011 of Japanese Patent No. 3376753, paragraph numbers of Japanese Patent No. 3319638 Those described in 0011 to 0026 and those described in paragraph Nos. 0006 to 0010 of Japanese Patent No. 3998630 can be used.

  The (A-1-2) component polycarbonate and organosiloxane copolymer are derived from an aromatic polycarbonate block and diorganosiloxane described in JP-A-10-7897, paragraphs 0010 to 0014. (8) Polysiloxane-polycarbonate copolymer-1, which is described in paragraph No. 0032 of the above publication, and a polycarbonate in which the amount of polydimethylsiloxane is 15% by weight of the whole copolymer -Organopolysiloxane copolymer (silicon content is 5.25 wt%), viscosity average molecular weight 22,000, (9) polysiloxane-polycarbonate copolymer-2, polydimethylsiloxane is 5 in the total amount of copolymer Polycarbonate-organopolysiloxane copolymer (silicon content) 1.75 wt%), it can be used viscosity-average molecular weight of 22,000.

Further, as the (A-1-2) component polycarbonate and organosiloxane copolymer, those described in paragraph Nos. 0027 to 0028 of JP-A No. 2010-280923 shown below can be used.
A polycarbonate and an organosiloxane copolymer are composed of a polycarbonate part and a polyorganosiloxane part. For example, a polyorganosiloxane having a reactive group at the terminal constituting a polycarbonate oligomer and a polyorganosiloxane part (polydimethylsiloxane, polyorganosiloxane) (Diethylsiloxane, polymethylphenylsiloxane, etc.) are dissolved in a solvent such as methylene chloride, an aqueous sodium hydroxide solution of bisphenol A is added, and an interfacial polycondensation reaction is performed using a catalyst such as triethylamine. . These polycarbonate and organosiloxane copolymers are disclosed in, for example, JP-A-3-292359, JP-A-4-202465, JP-A-8-81620, JP-A-8-302178, JP-A-10-7897. It is disclosed in the publication.
The degree of polymerization of the polycarbonate and the organosiloxane copolymer is preferably 3 to 100, and the degree of polymerization of the polydimethylsiloxane part is preferably about 2 to 500.
Further, the content of polydimethylsiloxane in the polycarbonate and the organosiloxane copolymer (including the by-produced bisphenol A polycarbonate) is usually 0.2 to 30% by mass, preferably 0.3 to 20% by mass. It is.

  Furthermore, what is described in Unexamined-Japanese-Patent No. 2011-46911 can be used as a polycarbonate and organosiloxane copolymer of (A-1-2) component.

  As the component (A-2), only a styrene resin may be used, only a polyester resin may be used, or a styrene resin and a polyester resin may be used in combination.

  (A-2) The component styrene resin includes ABS resin, AS resin, ASA resin, AES resin, ACS resin, ASS resin, PS resin, HIPS resin, MS resin, MBS resin, MABS resin, SB resin, SBS. Examples thereof include resin, SEBS resin, SIS resin, SIPS resin, and SEPS resin. The styrenic resin preferably contains an ABS resin and / or an AS resin.

  (A-2) The polyester resin of a component can use a well-known thing, for example, the aromatic polyester described in the paragraph numbers 0012-0017 of patent 3376753, the paragraph numbers 0027- of patent 3319638. Polyalkylene terephthalate described in No. 0032 and the thermoplastic polyester resin described in paragraph Nos. 0012 and 0013 of Japanese Patent No. 3998630 can be used. Preferably, polyethylene terephthalate, polypropylene terephthalate, polybutylene terephthalate, and polytrimethylene terephthalate can be used.

When the component (A) is composed of the component (A-1) and the component (A-2), the ratio of the component (A-1) to the component (A-2) in the component (A) is as follows:
(A-1) The ratio of a component is 50-98 mass%, Preferably it is 55-96 mass%,
(A-2) The ratio of a component is 50-2 mass%, Preferably it is 45-4 mass%.

[(B) component]
The fluidity improver of component (B) is a component that acts to increase the fluidity of the molten resin composition, and facilitates contact between the fiber bundle and the resin composition during the production of the resin-attached fiber bundle. It is also a component that acts like this.
(B) Component fluidity improvers include aromatic polyester oligomers, cyclic (alkylene terephthalate) oligomers, aromatic polycarbonate oligomers, polycaprolactone, low molecular weight acrylic copolymers, aliphatic rubber-polyester block copolymers. 1 type or 2 types or more selected are preferable.

As aromatic polyester oligomers, there are known aromatic dicarboxylic acids or ester-forming derivatives thereof and glycols or ester-forming derivatives thereof described in paragraph numbers 0051 to 0052 of JP-A-2003-26911. According to the method, a product produced by heating under pressure or slightly reduced pressure can be used.
The degree of polymerization of the aromatic polyester oligomer is determined to a desired value by adjusting the pressure, heating temperature and the like.
As the aromatic dicarboxylic acid, terephthalic acid is most preferable, and examples thereof include isophthalic acid and phthalic acid.
As the aromatic dicarboxylic acid or an ester-forming derivative thereof, an aromatic dicarboxylic acid dialkyl ester, acid chloride, or the like is preferable.
Examples of glycols or ester-forming derivatives thereof include ethylene glycol, 1,3-propanediol, 1,4-butanediol, 1,6-hexanediol, ethylene oxide, propylene oxide, and the like. At this time, a part of the glycol component may be replaced with glycerin, pentaerythritol, p-xylene glycol, 1,4-cyclohexanediol, bisphenol A, or the like.

As the cyclic (alkylene terephthalate) oligomer, those described in paragraph numbers 0012 to 0015 of JP2010-6920A can be used.
A mixture of cyclic oligomers having a polymerization degree of 2 to 30 and having a polymerization degree of up to 12 as the main component is preferred. Examples of commercially available products include CBT (cyclic poly (butylene terephthalate) oligomer; melting point 140 to 190 ° C.) manufactured by Cyclix Corporation.

  As the aromatic polycarbonate oligomer, those described in paragraph No. 0053 of JP-A No. 2003-26911 can be used.

  As polycaprolactone, what is described in Paragraph No. 0054 of Unexamined-Japanese-Patent No. 2003-26911 can be used.

As a low molecular weight acrylic copolymer, what is described in paragraph number 0055 of Unexamined-Japanese-Patent No. 2003-26911 can be used.
Specifically, it is a copolymer containing at least 7%, preferably 20 to 40% by weight of methacrylic acid or an ester of acrylic acid with an alcohol having 1 to 6 carbon atoms, and has a weight average molecular weight of 40,000 or less. , Preferably 25,000 or less. Examples of such acrylic acid esters include methyl acrylate, ethyl acrylate, propyl acrylate, butyl acrylate, and 1,3-butylene-diacrylate. Examples of the methacrylic acid ester include methyl methacrylate, ethyl methacrylate, butyl methacrylate, isobutyl methacrylate, and 1,3-butylene-dimethacrylate. Among them, butyl methacrylate is preferable. Components that copolymerize with these esters include vinyl monomers such as styrene, acrylonitrile, ethylene, propylene, butadiene, and butene-1, and preferred monomers are styrene and acrylonitrile.

As the aliphatic rubber-polyester block copolymer, those described in paragraph No. 0056 of JP-A No. 2003-26911 can be used.
Specifically, it is a block copolymer formed by ring-opening polymerization of an aliphatic lactone to an aliphatic diene rubber to form a polyester block, and the aliphatic diene rubber has a polyester block at one or both ends. It is a rubber-polyester block copolymer. The number average molecular weight of the aliphatic diene rubber is 1,000 to 4,000, and has functional groups such as a carboxykyl group, a hydroxyl group, a vinyl group, and an amino group at both ends of the molecule. Is preferred. Examples of the aliphatic diene rubber include α, ω-1,2-polybutadiene glycol, hydrogenated α, ω-1,2-polybutadiene glycol, hydroxyl-terminated modified 1,4-polybutadiene, liquid polychloroprene, and liquid natural rubber. Polybutadiene compounds or partially or completely hydrogenated polybutadiene compounds are preferred.
As the rubber-polyester block copolymer, an aliphatic diene rubber having a hydroxyl group at the terminal is preferably formed by sequentially ring-opening polymerizing an aliphatic lactone in the presence of a catalyst to form a polyester block at the terminal hydroxyl group. As the lactone, ε-caprolactone is preferred. The terminal group of the polyester chain in the block copolymer is usually a hydroxyl group, but it is desirable that the terminal group be blocked with a non-reactive group via an ester bond, an ether bond or a urethane bond.
Particularly preferred are those end-capped by acetylation with acetic anhydride and silyl etherification with a silylating agent.

  The content of the component (B) in the composition is preferably 0.5 to 20% by mass, more preferably 1 to 15% by mass, further preferably 2 in the total amount of the component (A) and the component (B). -10 mass%. Within the above range, fluidity when melt kneaded with the (A) component and the (D) component, and further with the (C) component as necessary can be improved, and therefore, the production of the resin-attached fiber bundle is facilitated. .

[Component (C)]
(C) The flame retardant of a component is a component used in providing flame retardance as needed.
(C) As a flame retardant of a component, a silicone type flame retardant is preferable. A well-known thing can be used for a silicone type flame retardant, For example, in the Example (paragraph number 0097) of the silicone type flame retardant described in Unexamined-Japanese-Patent No. 2005-320457, paragraph number 0051-0079, the said gazette. As substituents described in “X-40-9805” manufactured by Shin-Etsu Chemical Co., Ltd., “Trefill F202” manufactured by Toray Dow Corning Silicone Co., Ltd., paragraph No. 0012 of JP-A-2005-200508 Siloxane polymer having a methyl group and a phenyl group, “X-40-9805” manufactured by Shin-Etsu Chemical Co., Ltd. used in Examples, and paragraphs 0055 and 0056 of JP-A No. 2004-27113 Other than that, it is a siloxane polymer (silicone resin) with methyl and phenyl groups. It is possible to use the chemical industry Co., Ltd. KR-480.

  As for content of (C) component in a composition, 1-20 mass parts is preferable with respect to 100 mass parts of (A) component, More preferably, it is 2-15 mass parts, More preferably, it is 3-10 mass parts. .

[Component (D)]
As the reinforcing long fibers of component (D), known glass fibers, carbon fibers, metal fibers, inorganic fibers (excluding glass fibers) and the like can be used, but glass fibers are preferred.

As for content of (D) component in a composition, 12-240 mass parts is preferable with respect to 100 mass parts of (A) component, More preferably, it is 16-100 mass parts, More preferably, it is 24-67 mass parts. .
When the content of the component (D) is within the above range, the mechanical strength of the molded body can be increased, and the molding of the thin molded body is facilitated.

[Method for producing resin-attached fiber bundle]
The resin-attached fiber bundle is bundled in a state where the reinforcing long fibers for component (D) are aligned in the length direction, and the (A) component and (B) component are melted in the reinforcing long fiber bundle. (C) It can be obtained by adhering the components in a dispersed state and integrating them, and then cutting to a length of 3 to 30 mm.

  In the present invention, by using the fluidity improver of the component (B) as a component of the resin-attached fiber bundle, when the components (A) and (B) are further melted and kneaded, if necessary, the component (C) Since the fluidity is enhanced, the adhesion process of the components (A) and (B) to the reinforcing long fiber bundle composed of the component (D) and, if necessary, the component (C) is facilitated. The production of fiber bundles is also facilitated.

  The resin-attached fiber bundle can be manufactured by a well-known manufacturing method using a die. For example, paragraph number 7 of Patent Document 2 (Japanese Patent Laid-Open No. 6-31350), Patent Document 3 (Japanese Patent Laid-Open No. 2007-176227). In addition to paragraph No. 23 of Japanese Patent Publication No. 6-2344 (Manufacturing method and molding method of resin-coated long fiber bundle), JP-A-6-114732 (Fiber-reinforced thermoplastic resin structure and manufacturing method thereof) JP-A-6-293023 (manufacturing method of long fiber-reinforced thermoplastic resin composition), JP-A-7-205317 (method of taking out fiber bundles and manufacturing method of long fiber-reinforced resin structure), JP-A-7 -216104 (manufacturing method of long fiber reinforced resin structure), JP 7-251437 (manufacturing method and manufacturing apparatus of long fiber reinforced thermoplastic composite material), JP It can be applied to the manufacturing method described in such -118490 Patent Application (production method of the cross-head die and the long-fiber-reinforced resin structures).

  The length of the resin-attached fiber bundle (that is, the length of the reinforcing long fiber of component (D) contained in the resin-attached fiber bundle) is in the range of 3 to 30 mm, preferably 5 to 20 mm, more preferably 6 mm to 15 mm. If it is 3 mm or more, the mechanical strength of the molded product obtained from the composition can be increased, and if it is 30 mm or less, the moldability is improved.

  The diameter of the resin-attached fiber bundle is not particularly limited, but can be in the range of 0.5 mm to 5 mm.

  The remaining fiber length derived from the component (D) contained in the thin molded article of the present invention is preferably 0.3 to 1.5 mm, and more preferably 0.5 to 1.3 mm. Sufficient impact strength can be obtained within the above range.

<Other ingredients>
The composition of the present invention includes a flame retardant aid, a heat stabilizer, a lubricant, a light stabilizer, an antioxidant, a colorant, a release agent, an antistatic agent and the like within the scope that can solve the problems of the present invention. Can be contained.

<Thin-walled molded product and manufacturing method thereof>
The thin-walled molded article of the present invention can be manufactured by applying a known resin molding method such as an injection molding method using the above-mentioned resin-attached fiber bundle, and in addition, the (D) component contained in the molded body Since the length of the reinforcing fiber can be maintained longer, it can be manufactured by applying an injection compression molding method.

  The injection compression molding method is a known resin molding method. During resin filling, the cavity is temporarily enlarged slightly, and after filling without difficulty, a clamping mechanism or a hydraulic cylinder built into the mold, etc. Is a method of applying a predetermined shape by pressurizing and compressing a part or the entire surface of a molded product. The injection compression molding method is roughly divided from the viewpoint of the mold structure, and is divided into a low link method and a micromold method, and either method can be applied.

  Since the thin molded article of the present invention is thin and exhibits high mechanical strength, it is preferable that the thickness is 0.3 to 1.5 mm and the remaining fiber length is in the range of 0.3 to 1.5 mm.

The thin molded article of the present invention is suitable for an electronic device housing or an internal chassis.
Electronic devices include mobile phones, personal digital assistants (PDAs), smart phones, smart books, car navigation, game consoles, compact cassettes, CD players, DVD players, electronic notebooks, electronic dictionaries, calculators, hard disk recorders, personal computers, mobiles Listed are computers, tablet PCs, video cameras, and digital cameras.

Production Example 1 (Production of resin-impregnated glass long fiber bundle)
(A) Component, (A-2) Component and (B) component fluidity improver and (C) component flame retardant and other various additives are mixed in a tumbler with the formulation shown in Table 1. Thereafter, the mixture was melt-kneaded with a twin-screw extruder (270 ° C.) to obtain a pellet-shaped resin composition.
A fiber bundle (glass fiber 1: bundle of about 4000 fibers) bundled with a sizing agent composed of long glass fibers as component (D) was passed through a crosshead die. At that time, a melt kneaded product of the resin composition pellets shown in Table 1 is supplied to the crosshead die from another twin-screw extruder (cylinder temperature 290 ° C.) to impregnate the long glass fiber bundle of component (D). And a resin composition having a predetermined fiber content was obtained. Then, after shaping with a shaping nozzle at the outlet of the crosshead die and shaping with a shaping roll, the pellet was cut into a predetermined length with a pelletizer to obtain a pellet-shaped (columnar) resin-impregnated fiber bundle. When the resin-impregnated fiber bundle thus obtained was cut and confirmed, the long glass fibers were almost parallel to the length direction, and the resin was impregnated to the center.

Examples and Comparative Examples In Examples 1 to 9, the resin-impregnated fiber bundle obtained in Production Example 1 was used.
In Comparative Examples 1 to 3, an attempt was made to produce a resin-impregnated fiber bundle according to Production Example 1 using the components shown in Table 2, but the fiber bundle could not be impregnated with the polycarbonate resin.

<Measurement method>
(1) Weight average fiber length Test piece preparation method An ISO multipurpose test piece A-shaped product (thickness 4 mm) was prepared under the following conditions.

Apparatus: J-150EII manufactured by Nippon Steel Works
Cylinder temperature 280 ° C
Mold temperature: 100 ° C
Screw: Screw for long fibers Screw diameter: 51mm
Gate shape 20 mm wide side gate A sample of about 3 g was cut out from the above test piece, heated at 650 ° C. to be ashed, and the fiber was taken out. The weight average fiber length was determined from a part (500) of the extracted fibers. As the calculation formula, [0044] and [0045] of JP-A-2006-274061 were used.

(2) Tensile strength (MPa)
The measurement was performed according to ISO527.
(3) Bending strength (MPa)
Measurement was performed in accordance with ISO178.
(4) Flexural modulus (MPa)
Measurement was performed in accordance with ISO178.
(5) Charpy impact strength (kJ / m ² )
The notched Charpy impact strength was measured according to ISO 179 / 1eA.
(6) Heat resistance (deflection temperature under load)
Based on ISO75, the load was evaluated at 1.80 MPa.
(7) Flame retardancy In a UL94 vertical combustion test (V-0 to V-2), a test piece having a thickness of 1.2 mm prepared from the compositions of Examples and Comparative Examples was tested.

<Use ingredients>
Component (A-1) PC-1: Mitsubishi Engineering Plastics Co., Ltd., Iupilon S2000F, viscosity average molecular weight of about 22000
PC-2: Mitsubishi Engineering Plastics, Iupilon S3000F, viscosity average molecular weight of about 18000
(A-2) Component ABS-1: Emulsion polymerization ABS resin (40% by mass of rubber, 26% by mass of acrylonitrile)
AS: Sebian N 050 manufactured by Daicel Polymer Co., Ltd.
PET: Belpet EFG6C manufactured by Bell Polyester Products
(B) Component Polycaprolactone: Placel H1P manufactured by Daicel Corporation
Cyclic polyester oligomer: CBT100 made by CYCLICS CORPRATION
Component (C) Glass fiber 1: Glass fiber roving, fiber diameter 17 μm, bundled with epoxy silane coupling agent (D) Component Methylphenylsilicone resin: KR-480 manufactured by Shin-Etsu Chemical Co., Ltd.
(Other)
PTFE: Asahi Glass Co., Ltd. Fluon PTFE CD141
Stabilizer 1: BASF Japan, Irganox 1010
Stabilizer 2: ADEKA Corporation, ADK STAB PEP36
Stabilizer 3: Made by ADEKA, Adeka Stub AX71
Olefin wax: Honeywell International, Inc. Made of AC polyethylene 9A
Talc: Hayashi Kasei Co., Ltd., Micron White 5000S

  In Tables 1 and 2, (A-1) component, (A-2) component, and (B) component are expressed in mass%, and the other components are (A-1) component and (A-2) component. And (B) parts by mass with respect to 100 parts by mass in total. Therefore, in the case of Example 8, the content ratio of the component (C) in the resin-impregnated fiber bundle is 3.9% by mass, and the component (D) is 40% by mass.

Claims (9)

(A) Thermoplastic resin containing only polycarbonate resin, (B) Cyclic (alkylene terephthalate) oligomer, aromatic polycarbonate oligomer, polycaprolactone, low molecular weight acrylic copolymer, aliphatic rubber-polyester block copolymer A resin composition comprising a resin-attached long fiber bundle containing one or more fluidity improvers and optionally (C) a flame retardant, and (D) glass fibers which are reinforcing long fibers. Because
The resin-attached long fiber bundle is a bundle of glass fibers that are reinforcing long fibers of component (D) aligned in the length direction, and the bundle of glass fibers that are reinforcing long fibers is combined with component (A) and ( B) The component is melted, and other components selected from flame retardant aids, heat stabilizers, lubricants, light stabilizers, antioxidants, colorants, mold release agents, and antistatic agents, and if necessary (C ) A resin composition obtained by cutting a 3-30 mm length of an integrated and adhered component in a dispersed state.   The resin composition of Claim 1 whose flame retardant of (C) component is a silicone type flame retardant.   Resin-attached long fiber bundle is a reinforcing long fiber bundle in which the reinforcing long fibers of component (D) are aligned in the length direction. In a state in which the components including the component are melted, the surface of the reinforcing long fiber bundle is coated and impregnated into the reinforcing long fiber bundle to be integrated and cut into a length of 3 to 30 mm. The resin composition according to claim 1 or 2.   Resin-attached long fiber bundle is a reinforcing long fiber bundle in which the reinforcing long fibers of component (D) are aligned in the length direction. In a state in which the components including the component are melted, the surface of the reinforcing long fiber bundle is coated and integrated without impregnation into the reinforcing long fiber bundle, and is cut to a length of 3 to 30 mm. The resin composition according to claim 1 or 2.   The resin composition according to any one of claims 1 to 4, wherein the resin-attached long fiber bundle has a diameter of 0.5 to 5 mm and a length of 3 to 30 mm.   A thin molded article comprising the resin composition according to any one of claims 1 to 5, having a thickness of 0.3 to 1.5 mm and a remaining fiber length of 0.3 to 1.5 mm. The thin-walled molded product according to claim 6 , wherein the thin-walled molded product is for a housing of an electronic device or an internal chassis.   Electronic devices are mobile phones, personal digital assistants (PDAs), smart phones, car navigation systems, game machines, compact cassettes, CD players, DVD players, electronic notebooks, electronic dictionaries, calculators, hard disk recorders, personal computers, video cameras, digital cameras The thin-walled molded article according to claim 7, which is selected from the following. A method for producing a thin molded product according to claim 6 or 8, wherein the resin composition according to any one of claims 1 to 5 is used.
A method for producing a thin molded article, wherein the resin composition is molded by an injection molding method or an injection compression molding method.