JP2014133790A - Polyester resin composition for wattmeter outer package - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a polyester resin composition excellent in shock resistance, thermal aging resistance, low warpage property, hydrolysis resistance, fire resistance, weather resistance, appearance and the like and useful as for a wattmeter outer package.SOLUTION: A polyester resin composition for a wattmeter outer package contains 100 pts.mass of a polybutylene terephthalate resin (A), 20 to 80 pts.mass of a styrene copolymer (B), 0 to 30 pts.mass of a compatibilizer (C), 15 to 130 pts.mass of a reinforcement filler (D), 10 to 45 pts.mass of a bromine-based fire retardant (E) and 3 to 30 pts.mass of an antimony-based fire retardant assistant (F), 0.1 to 5 pts.mass of an acrylonitrile-styrene resin and 0.001 to 3 pts.mass of carbon black (H).

Description

  The present invention relates to a polyester resin composition for exterior wattmeters, and more specifically, particularly excellent in impact resistance, heat aging resistance, low warpage, hydrolysis resistance, flame resistance, weather resistance, appearance, and the like. The present invention relates to a polyester resin composition for use as a power meter exterior.

  Thermoplastic polyester resins typified by polybutylene terephthalate have excellent mechanical strength, chemical resistance, electrical insulation, etc., and have excellent heat resistance, moldability, and recyclability. It is used indoors and outdoors for materials, electrical and electronic equipment materials, housing materials, and other parts manufacturing materials in industrial fields. In particular, resin molded bodies for outdoor use are required to have impact resistance, heat aging resistance (heat stability), low warpage, flame retardancy, and the like.

  The present applicant previously proposed in Patent Document 1 that a resin composition in which a rubber-modified polystyrene resin and a polycarbonate resin are blended with a polybutylene terephthalate resin is excellent in moldability, strength and impact resistance, Patent Document 2 proposes a resin composition that is excellent in moldability and impact resistance and has little warpage, in which a polybutylene terephthalate resin is blended with a rubber-modified polystyrene resin, a polycarbonate resin, and a reinforcing filler.

  Examples of outdoor use include outdoor use (installation) equipment parts such as a power meter (also called a power meter or an electric meter). Molded parts for wattmeter exteriors such as wattmeter covers and housings are required to have high impact resistance, strength, heat aging resistance (heat stability), low warpage, and the like. In recent years, power supply problems and energy saving have become social issues, and electric power companies have been spreading digital smart electric meters (also referred to as “smart meters” for short). The consumption is reported to the user and the power company, and the power company can predict or manage the power consumption during the peak hour period.

  Such a smart meter is packaged with a resin material, and the standard specification is required to have higher strict impact resistance compared to the product standard of a conventional power meter. In particular, surface impact, which is one of the impact resistance indicators, does not correspond one-to-one with normal Charpy impact values, etc. Especially, smart meter exterior injection molded products usually require a large number of pin gates. Therefore, it is not easy to achieve high surface impact by orientation from the pin gate, and it is necessary to considerably improve the weld strength and the like.

  From such a point of view, the resin composition proposed in Patent Document 1 or Patent Document 2 has insufficient impact resistance, and in particular, the surface impact property cannot pass the level required for smart meters. In addition, heat aging resistance, low warpage, hydrolysis resistance, flame retardancy, weather resistance, appearance, etc. were not sufficient.

JP 2002-127552 A JP 2002-12753 A

  The object of the present invention is to provide a polyester resin composition that is excellent in impact resistance, heat aging resistance, low warpage, hydrolysis resistance, flame retardancy, weather resistance, appearance, etc. It is to provide.

The inventor has added a styrene copolymer, a reinforcing filler, a brominated flame retardant, an antimony flame retardant auxiliary, an acrylonitrile-styrene resin and carbon black to the polybutylene terephthalate resin, if necessary. The present inventors have found that polyester resin compositions each containing a specific amount of solubilizer can solve the above-mentioned problems.
The present invention provides the following polyester resin composition for exterior wattmeters.

[1] 20 to 80 parts by mass of a styrene copolymer (B), 0 to 30 parts by mass of a compatibilizer (C), and 15 to 15 parts of a reinforcing filler (D) with respect to 100 parts by mass of the polybutylene terephthalate resin (A). 130 parts by mass, brominated flame retardant (E) 10 to 45 parts by mass, antimony flame retardant auxiliary (F) 3 to 30 parts by mass, acrylonitrile-styrene resin (G) 0.1 to 5 parts by mass and carbon black ( H) A polyester resin composition for wattmeter exterior, characterized by containing 0.001 to 3 parts by mass.
[2] The wattmeter exterior polyester resin composition according to [1], wherein the content of the compatibilizing agent (C) is 5 to 25 parts by mass with respect to 100 parts by mass of the polybutylene terephthalate resin (A).
[3] The polyester resin composition for exterior wattmeters according to the above [1] or [2], wherein the compatibilizer (C) is an aromatic polycarbonate resin.
[4] The polyester resin composition for exterior wattmeters according to any one of [1] to [3], wherein the aromatic polycarbonate resin has a viscosity average molecular weight (Mv) of 23,000 to 35,000.
[5] The wattmeter according to any one of [1] to [4], wherein the brominated flame retardant (E) is pentabromobenzyl polyacrylate, brominated polystyrene, brominated epoxy compound, or brominated aromatic polycarbonate oligomer. A polyester resin composition for exterior use.

The polyester resin composition of the present invention is excellent in impact resistance, heat aging resistance, low warpage, hydrolysis resistance, flame retardancy, weather resistance, appearance, and the like.
For this reason, the polyester resin composition of this invention can be used conveniently for the cover of a wattmeter, a housing | casing, etc. as a molded product for wattmeter exteriors. The molded product for wattmeters tends to be cracked with a large number of gates, but by using the resin composition of the present invention, impact resistance is remarkably improved, cracks are reduced, and heat resistance, It becomes possible to obtain a molded article for a wattmeter exterior that is excellent in flame retardancy, heat aging resistance, hydrolysis resistance and dimensional stability. In addition, weather resistance is required for outdoor use, but it is excellent in weather resistance, and the compatibilizer blended as needed functions effectively. Therefore, the resin composition of the present invention can be preferably used because there is no problem of poor appearance due to powder blowing caused by bleeding out of the slag.

[Summary of Invention]
The polyester resin composition for exterior wattmeters of the present invention is 20 to 80 parts by mass of a styrene copolymer (B) and 0 to 30 parts by mass of a compatibilizer (C) with respect to 100 parts by mass of the polybutylene terephthalate resin (A). Parts, reinforcing filler (D) 15-130 parts by weight, brominated flame retardant (E) 10-45 parts by weight, antimony flame retardant auxiliary (F) 3-30 parts by weight, acrylonitrile-styrene resin (G) It contains 0.1 to 5 parts by mass and 0.001 to 3 parts by mass of carbon black (H).

Hereinafter, the contents of the present invention will be described in detail.
The description of each constituent element described below may be made based on typical embodiments and specific examples of the present invention, but the present invention is interpreted to be limited to such embodiments and specific examples. It is not a thing. In the specification of the present application, “to” is used in the sense of including the numerical values described before and after it as the lower limit value and the upper limit value.

[Polybutylene terephthalate resin (A)]
The polybutylene terephthalate resin (A) which is the main component of the polyester resin composition of the present invention is a polycondensation of a dicarboxylic acid compound containing terephthalic acid as a main component and a diol compound containing 1,4-butanediol as a main component. Polyester obtained by polycondensation or the like, and may be either homopolyester or copolyester.

As the dicarboxylic acid compound other than terephthalic acid constituting the polybutylene terephthalate resin (A), an aromatic dicarboxylic acid other than terephthalic acid or an ester-forming derivative thereof is preferably used.
As aromatic dicarboxylic acids, isophthalic acid, orthophthalic acid, 1,5-naphthalenedicarboxylic acid, 2,5-naphthalenedicarboxylic acid, 2,6-naphthalenedicarboxylic acid, biphenyl-2, 2'-dicarboxylic acid, biphenyl-3 , 3′-dicarboxylic acid, biphenyl-4,4′-dicarboxylic acid, diphenyl ether-4,4′-dicarboxylic acid, diphenylmethane-4,4′-dicarboxylic acid, diphenylsulfone-4,4′-dicarboxylic acid, diphenylisopropyl Redene-4,4′-dicarboxylic acid, 1,2-bis (phenoxy) ethane-4,4′-dicarboxylic acid, anthracene-2,5-dicarboxylic acid, anthracene-2,6-dicarboxylic acid, p-terphenylene Examples include -4,4'-dicarboxylic acid and pyridine-2,5-dicarboxylic acid.

These aromatic dicarboxylic acids may be used as a mixture of two or more. As is well known, these can be used in polycondensation reactions as ester-forming derivatives such as dimethyl esters in addition to free acids.
In a small amount, aliphatic dicarboxylic acids such as adipic acid, azelaic acid, dodecanedioic acid, sebacic acid, 1,2-cyclohexanedicarboxylic acid, 1,3-cyclohexanedicarboxylic acid and 1,4-cyclohexanedicarboxylic acid 1 or more types of alicyclic dicarboxylic acids, such as these, can be mixed and used.

Examples of diol compounds other than 1,4-butanediol constituting the polybutylene terephthalate resin (A) include ethylene glycol, propylene glycol, hexylene glycol, neopentyl glycol, 2-methylpropane-1,3-diol, diethylene glycol, Examples include aliphatic diols such as triethylene glycol, alicyclic diols such as cyclohexane-1,4-dimethanol, and mixtures thereof. If the amount is small, one or more kinds of long-chain diols having a molecular weight of 400 to 6,000, that is, polyethylene glycol, poly-1,3-propylene glycol, polytetramethylene glycol, and the like may be copolymerized.
In addition, aromatic diols such as hydroquinone, resorcin, naphthalenediol, dihydroxydiphenyl ether, and 2,2-bis (4-hydroxyphenyl) propane can also be used.

  In addition to the above-mentioned bifunctional monomers, trifunctional monomers such as trimellitic acid, trimesic acid, pyromellitic acid, pentaerythritol, and trimethylolpropane are introduced to introduce a branched structure, and fatty acids are used for molecular weight control. A small amount of a monofunctional compound can be used in combination.

  As polybutylene terephthalate resin (A), it is usually preferable that 50 mass%, preferably 70 mass% or more of the whole resin is derived from terephthalic acid and 1,4-butanediol. Of these, those in which 95 mol% or more of the acidic component is derived from terephthalic acid and 95 mass% or more of the alcohol component are derived from 1,4-butanediol are preferred.

  The intrinsic viscosity ([η]) of the polybutylene terephthalate resin (A) is preferably 0.5 to 2 dl / g. From the viewpoint of moldability and mechanical properties, those having an intrinsic viscosity in the range of 0.6 to 1.5 dl / g are preferred. If the intrinsic viscosity is lower than 0.5 dl / g, the resulting resin composition tends to have a low mechanical strength. On the other hand, if it is higher than 2 dl / g, the fluidity of the resin composition may deteriorate and the moldability may deteriorate. The intrinsic viscosity of the polyester resin is measured at 30 ° C. in a 1: 1 (mass ratio) mixed solvent of 1,1,2,2-tetrachloroethane and phenol.

[Styrene copolymer (B)]
Examples of the styrene copolymer (B) used in the present invention include a copolymer of a styrene monomer and another copolymerizable monomer, and a styrene graft copolymer.
More specifically, examples of the styrene copolymer (B) include high impact polystyrene (HIPS), acrylonitrile-butadiene-styrene copolymer (ABS resin), and methyl methacrylate-butadiene-styrene copolymer (MBS resin). ), Methyl methacrylate-acrylonitrile-butadiene-styrene copolymer (MABS resin), acrylonitrile-acrylic rubber-styrene copolymer (AAS resin), acrylonitrile-ethylenepropylene rubber-styrene copolymer (AES resin), styrene- Examples thereof include resins such as an IPN type rubber copolymer. Among these, impact resistant polystyrene (HIPS) and acrylonitrile-butadiene-styrene copolymer (ABS resin) are preferable.

  The content of the rubber component in the styrene-based copolymer is preferably 3 to 70% by mass, more preferably 5 to 50% by mass, and further preferably 7 to 30% by mass. When the content of the rubber component is less than 3% by mass, the impact resistance may be lowered, and when it exceeds 50% by mass, the flame retardancy tends to be lowered. Moreover, it is preferable that the average particle diameter of a rubber component is 0.05-10 micrometers, It is more preferable that it is 0.1-6 micrometers, It is further more preferable that it is 0.2-3 micrometers. If the average particle size is less than 0.05 μm, impact resistance tends to be lowered, and if it exceeds 10 μm, glossiness is lost and a good appearance may not be obtained.

  The mass average molecular weight of the styrenic copolymer (B) is usually 50,000 or more, preferably 100,000 or more, more preferably 150,000 or more, and the upper limit is usually 500. , 000 or less, preferably 400,000 or less, more preferably 300,000 or less. The number average molecular weight is usually 10,000 or more, preferably 30,000 or more, more preferably 50,000 or more, and the upper limit is usually 300,000 or less. Is 200,000 or less, more preferably 150,000 or less. By using such a styrene copolymer (B), low warpage is easily imparted, which is preferable.

  The melt flow rate (MFR) of the styrene copolymer (B) measured in accordance with JIS K7210 (temperature 200 ° C., load 5 kgf) is preferably 0.1 to 30 g / 10 min. More preferably, it is 5 to 25 g / 10 min. If the MFR is less than 0.1 g / 10 minutes, the fluidity may be lowered, and if it exceeds 30 g / 10 minutes, the impact resistance tends to be lowered, which is not preferable.

  Examples of the method for producing such a styrene copolymer (B) include known methods such as an emulsion polymerization method, a solution polymerization method, a suspension polymerization method, and a bulk polymerization method.

The styrenic copolymer (B) comprises a polymer block mainly composed of a vinyl aromatic compound such as styrene and a polymer block mainly composed of an unhydrogenated and / or hydrogenated conjugated diene compound. Block copolymers can also be used.
Examples of the vinyl aromatic compound constituting the block copolymer include styrene, α-methyl styrene, vinyl toluene, p-tertiary butyl styrene, divinyl benzene, p-methyl styrene, 1,1-diphenyl styrene, and the like. One or two or more types can be selected from among them, and styrene is preferable among them. Examples of the conjugated diene compound include butadiene, isoprene, 1,3-pentadiene, 2,3-dimethyl-1,3-butadiene, pyrylene, 3-butyl-1,3-octadiene, phenyl-1,3- One or two or more types are selected from butadiene and the like, and among them, butadiene, isoprene and combinations thereof are preferable.
The block copolymer here is a block copolymer composed of a polymer block A mainly composed of a vinyl aromatic compound and a polymer block B mainly composed of a conjugated diene compound. The copolymerization ratio of the conjugated diene compound is preferably 5/95 to 70/30, and particularly preferably 10/90 to 60/40.

The number average molecular weight of the block copolymer is in the range of 5,000 to 600,000, preferably 10,000 to 500,000, and the molecular weight distribution [mass average molecular weight (Mw) and number average molecular weight (Mn) Ratio (Mw / Mn)] is 10 or less. The molecular structure of the block copolymer may be linear, branched, radial, or any combination thereof. For example, vinyl aromatic compound-conjugated diene compound block copolymer having a structure such as ABA, BABA, (ABA) ₄ Si, ABABABA, etc. It is a coalescence. Furthermore, the unsaturated bond of the conjugated diene compound of the block copolymer may be partially hydrogenated.

  The method for producing such a block copolymer is not particularly limited as long as the method having the structure described above can be obtained. For example, a vinyl aromatic compound-conjugated diene compound block in an inert solvent using a lithium catalyst or the like by the method described in JP-B-40-23798, JP-B-43-1779, and JP-B-56-28925 Copolymers can be synthesized. Furthermore, hydrogenation is carried out in the presence of a hydrogenation catalyst in an inert solvent by the method described in JP-B-42-8704, JP-B-43-6636, or JP-B-59-133203. Partially hydrogenated block copolymers for use in the invention can be synthesized.

  An epoxy-modified block copolymer obtained by epoxidizing the above block copolymer can also be used as the styrenic copolymer (B) of the present invention. The epoxy-modified block copolymer can be obtained by reacting the above block copolymer with an epoxidizing agent such as hydroperoxides and peracids in an inert solvent. Hydroperoxides include hydrogen peroxide, tertiary butyl hydroperoxide, cumene peroxide and the like. Examples of peracids include performic acid, peracetic acid, perbenzoic acid, and trifluoroperacetic acid. Of these, peracetic acid is a preferred epoxidizing agent because it is industrially produced in large quantities, is available at low cost, and has high stability.

  In the epoxidation, a catalyst can be used as necessary. For example, in the case of a peracid, an alkali such as sodium carbonate or an acid such as sulfuric acid can be used as a catalyst. In the case of hydroperoxides, a catalytic effect can be obtained by using a mixture of tungstic acid and caustic soda in combination with hydrogen peroxide or molybdenum hexacarbonyl in combination with tertiary butyl hydroperoxide. There is no strict regulation of the amount of epoxidizing agent, and the optimum amount in each case depends on variables such as the particular epoxidizing agent used, the desired degree of epoxidation, and the particular block copolymer used.

  As the inert solvent, it can be used for the purpose of reducing the viscosity of the raw material, stabilizing by diluting the epoxidizing agent, and in the case of peracetic acid, ethers, esters, etc. can be used if it is an aromatic compound. it can. Particularly preferred solvents are hexane, cyclohexane, toluene, benzene, ethyl acetate, carbon tetrachloride, and chloroform. There are no strict regulations on the epoxidation reaction conditions. The reaction temperature range that can be used is determined by the reactivity of the epoxidizing agent used. For example, in the case of peracetic acid, 0 to 70 ° C. is preferable. If it is lower than 0 ° C., the reaction is slow, and if it exceeds 70 ° C., decomposition of peracetic acid occurs. Moreover, in the tertiary butyl hydroperoxide / molybdenum dioxide diacetylacetonate system which is an example of hydroperoxide, 20-150 degreeC is preferable for the same reason. No special operation of the reaction mixture is necessary. For example, the mixture may be stirred for 2 to 10 hours. Isolation of the obtained epoxy-modified copolymer is an appropriate method, for example, a method of precipitating with a poor solvent, a method of pouring the polymer into hot water with stirring and distilling off the solvent, a direct desolvation method, etc. Can be done.

  Content of a styrene-type copolymer (B) is 20-80 mass parts with respect to 100 mass parts of polybutylene terephthalate resins (A). When the content of the styrenic copolymer (B) is less than 20 parts by mass, the warpage of the molded product may increase, and when it exceeds 80 parts by mass, the heat resistance tends to decrease. The content of the styrene copolymer (B) is preferably 70 parts by mass or less, more preferably 60 parts by mass or less, preferably 30 parts by mass or more, more preferably 40 parts by mass or more. Moreover, you may use a styrene-type copolymer (B) in mixture of 2 or more types.

[Compatibilizer (C)]
The polyester resin composition of the present invention preferably contains a compatibilizer (C). Examples of the compatibilizer (C) include aromatic polycarbonate resins, unsaturated (anhydrous) carboxylic acid-modified styrene resins, glycidyl-modified styrene resins, and the like. Among these, an aromatic polycarbonate resin is preferable.

  Examples of the aromatic polycarbonate resin include an aromatic polycarbonate resin, an aliphatic polycarbonate resin, and an aromatic-aliphatic polycarbonate resin, preferably an aromatic polycarbonate resin. Specifically, an aromatic dihydroxy compound is converted to phosgene or A thermoplastic aromatic polycarbonate polymer or copolymer obtained by reacting with a diester of carbonic acid is used.

  Examples of the aromatic dihydroxy compound include 2,2-bis (4-hydroxyphenyl) propane (bisphenol A), tetramethylbisphenol A, α, α′-bis (4-hydroxyphenyl) -p-diisopropylbenzene, hydroquinone, Resorcinol, 4,4′-dihydroxydiphenyl and the like can be mentioned. In addition, as a part of the dihydroxy compound, a compound in which one or more tetraalkylphosphonium sulfonates are bonded to the above aromatic dihydroxy compound, or a polymer or oligomer having a siloxane structure and containing both terminal phenolic OH groups Is preferable because of its high flame retardancy.

  Preferable examples of the aromatic polycarbonate resin include 2,2-bis (4-hydroxyphenyl) propane as a dihydroxy compound or a polycarbonate using 2,2-bis (4-hydroxyphenyl) propane in combination with another aromatic dihydroxy compound. Resin.

  The aromatic polycarbonate resin may be a homopolymer composed of one type of repeating unit or a copolymer having two or more types of repeating units. At this time, the copolymer can be selected from various copolymerization forms such as a random copolymer and a block copolymer.

The molecular weight of the aromatic polycarbonate resin is not limited, but using methylene chloride as a solvent, the viscosity average molecular weight (Mv) converted from the solution viscosity measured at a temperature of 20 ° C., preferably 10,000 to 40,000, More preferably, it is 14,000 or more, More preferably, it is 16,000 or more, Most preferably, it is 23,000 or more, More preferably, it is 39,000 or less, More preferably, it is 38,000 or less, Most preferably, it is 35,000 or less. is there. When the viscosity average molecular weight is in such a range, the resulting polyester resin composition has good moldability and a molded product having high mechanical strength is easily obtained.
In the present invention, the viscosity average molecular weight (Mv) of the aromatic polycarbonate resin is determined by measuring the viscosity of the methylene chloride solution of the polycarbonate resin at 20 ° C. using an Ubbelohde viscometer, and calculating the intrinsic viscosity ([η]). The value calculated from the following Schnell viscosity equation is shown.
[Η] = 1.23 × 10 ⁻⁴ Mv ^0.83

  The method for producing the aromatic polycarbonate resin is not particularly limited, and a polycarbonate resin produced by any of the phosgene method (interfacial polymerization method) and the melting method (transesterification method) can also be used. Moreover, the polycarbonate resin which performed the post-process which adjusts the amount of terminal OH groups to the polycarbonate resin manufactured by the melting method is also preferable.

The unsaturated (anhydrous) maleic acid-modified styrene resin means a resin obtained by modifying a styrene resin with an unsaturated carboxylic acid, an unsaturated carboxylic acid anhydride, or a derivative thereof.
Examples of unsaturated carboxylic acids, unsaturated carboxylic acid anhydrides or derivatives thereof include (anhydrous) maleic acid, (anhydrous) itaconic acid, chloro (anhydrous) maleic acid, (anhydrous) citraconic acid, butenyl (anhydrous) succinic acid, tetrahydro (Anhydrous) phthalic acid and these acid halides, amides, imides, C1-C20 alkyl or glycol esters, specifically maleimide, monomethyl maleate, dimethyl maleate and the like. Here, “(anhydrous)” indicates anhydrous unsaturated carboxylic acid or unsaturated carboxylic acid. Of these, unsaturated dicarboxylic acids or acid anhydrides thereof are preferred, (anhydrous) maleic acid or (anhydrous) itaconic acid is more preferred, and maleic anhydride is still more preferred. These unsaturated carboxylic acids, unsaturated carboxylic acid anhydrides or derivatives thereof may be used in combination of two or more.

The glycidyl-modified styrene resin refers to a resin obtained by modifying a styrene resin with a glycidyl group-containing compound such as glycidyl ethers or glycidyl esters.
Examples of glycidyl ethers include monoglycidyl ethers such as methyl glycidyl ether, butyl glycidyl ether, 2-ethylhexyl glycidyl ether, decyl glycidyl ether, stearyl glycidyl ether, phenyl glycidyl ether, butylphenyl glycidyl ether, and allyl glycidyl ether; Examples thereof include diglycidyl ethers such as glycidyl ether, ethylene glycol diglycidyl ether, glycerin diglycidyl ether, propylene glycol diglycidyl ether, and bisphenol A diglycidyl ether.
Examples of glycidyl esters include monoglycidyl esters such as glycidyl benzoate and glycidyl sorbate; diglycidyl esters such as adipic acid diglycidyl ester, terephthalic acid diglycidyl ester and orthophthalic acid diglycidyl ester. It is done. Two or more of these glycidyl group-containing compounds may be used in combination.

The styrene resin used in the unsaturated (anhydrous) carboxylic acid-modified styrene resin and the glycidyl-modified styrene resin is a homopolymer of an aromatic vinyl monomer or a copolymer with a monomer copolymerizable therewith. Refers to coalescence.
Examples of aromatic vinyl monomers include styrene, α-methylstyrene, p-methylstyrene, o-methylstyrene, t-butylstyrene, o-ethylstyrene, p-chlorostyrene, o-chlorostyrene, 2,4 -Dichlorostyrene, p-methoxystyrene, o-methoxystyrene, 2,4-dimethylstyrene, etc. are mentioned, and among these, styrene is preferable. Two or more of these monomers may be mixed and used.

  Examples of monomers that can be copolymerized with aromatic vinyl monomers include methyl acrylate, methyl methacrylate, ethyl acrylate, ethyl methacrylate, butyl acrylate, butyl methacrylate, 2-ethylhexyl acrylate, (Meth) acrylic acid ester monomers such as 2-ethylhexyl methacrylate, dodecyl acrylate, dodecyl methacrylate, tridecyl acrylate, tridecyl methacrylate, octadecyl acrylate, octadecyl methacrylate, cyclohexyl acrylate, cyclohexyl methacrylate ; Vinyl cyanide monomers such as acrylonitrile and methacrylonitrile; maleimide monomers such as N-phenylmaleimide, N-methylmaleimide and N-cyclohexylmaleimide; vinylmethylether and vinylethylether Vinyl ether monomers such as vinyl acetate, vinyl butyrate and other carboxylate monomers; ethylene, propylene, isobutylene and other olefin monomers; butadiene, isoprene, dimethylbutadiene and other diene monomers Can be mentioned. Two or more of these monomers may be mixed and used.

  The styrene resin has a mass average molecular weight of usually 50,000 or more, preferably 100,000 or more, more preferably 150,000 or more, and the upper limit is usually 500,000. Yes, preferably 400,000, more preferably 300,000.

  Examples of the method for producing such a styrene resin include known methods such as an emulsion polymerization method, a solution polymerization method, a suspension polymerization method, and a bulk polymerization method. Two or more styrenic resins may be mixed and used.

  The method for producing the unsaturated (anhydrous) carboxylic acid-modified polystyrene resin and the glycidyl-modified polystyrene resin is not particularly limited, and a conventionally known method can be employed. For example, it can be produced by weighing and mixing a predetermined amount of a styrenic resin with the unsaturated carboxylic acid, unsaturated carboxylic acid anhydride or derivative thereof, or a glycidyl group-containing compound modifier and reacting in a molten state. . The blending amount of the modifier is preferably 1 to 20 parts by mass, more preferably 3 to 12 parts by mass, and further preferably 6 to 10 parts by mass with respect to 100 parts by mass of the styrene resin.

In modification, a radical generator may be added at the same time as the modifying agent. Examples of the radical generator include organic peroxides and azo compounds.
Specific examples of the organic peroxide include, for example, t-butyl hydroperoxide, cumene hydroperoxide, 2,5-dimethylhexane-2,5-dihydroperoxide, 1,1,3,3-tetramethyl. Hydroperoxides such as butyl hydroperoxide, p-menthane hydroperoxide, diisopropylbenzene hydroperoxide, 2,5-dimethyl-2,5-di (t-butylperoxy) hexyne-3, di-t- Dialkyl peroxides such as butyl peroxide, t-butylcumyl peroxide, 2,5-dimethyl-2,5-di (t-butylperoxy) hexane, dicumyl peroxide, 2,2-bis-t- Butyl peroxybutane, 2,2-bis-t-butyl peroxyoctane, 1, -Peroxyketals such as bis-t-butylperoxycyclohexane and 1,1-bis-t-butylperoxy-3,3,5-trimethylcyclohexane, di-t-butylperoxyisophthalate, t-butyl Peroxyesters such as peroxybenzoate, t-butylperoxyacetate, 2,5-dimethyl-2,5-dibenzoylperoxyhexane, t-butylperoxyisopropyl carbonate, t-butylperoxyisobutyrate, Examples include diacyl peroxides such as benzoyl peroxide, m-toluoyl peroxide, acetyl peroxide, and lauroyl peroxide.

  Specific examples of the azo compound include 2,2′-azobisisobutyronitrile, 2,2′-azobis (2-methylbutyronitrile), 1,1′-azobis (cyclohexane-1-carbonitrile), 1-[(1-cyano-1-methylethyl) azo] formamide, 2-phenylazo-4-methoxy-2,4-dimethylvaleronitrile, 2,2′-azobis (2,4,4-trimethylpentane), 2,2′-azobis (2-methylpropane) and the like.

  Among these radical generators, particularly preferred are radical generators having a half-life temperature of 120 ° C. or more in 10 hours from the viewpoint of dimensional stability and impact resistance. The blending amount of the radical generator is preferably 0.01 to 5 parts by mass, more preferably 0.05 to 3 parts by mass, and still more preferably 0.1 to 1 part by mass with respect to 100 parts by mass of the styrene resin. .

  As a specific method of reacting in the molten state, there is a method of mixing and reacting in the molten state. In order to mix and react in a molten state, a melt kneader generally used for thermoplastic resins can be used. A modification reaction takes place during melting in a melt kneader. Examples of the melt kneader include a single-screw or multi-screw extruder, a roll, and a Banbury mixer. In the case of using an extruder, for example, a method in which the respective components are mixed in advance with a blender or the like, and the obtained mixture is collectively fed (feeded) on the upstream side of the extruder and reacted in a molten state is preferable.

  The modified styrene resin thus obtained has a mass average molecular weight of usually 50,000 or more, preferably 100,000 or more, more preferably 150,000 or more, and the upper limit is Usually, it is 500,000 or less, preferably 400,000 or less, more preferably 300,000 or less. If the mass average molecular weight is less than 50,000, impact resistance tends to be lowered, and if it exceeds 500,000, fluidity may be lowered.

  Further, the melt flow rate (MFR) of the modified styrene resin measured in accordance with JIS K7210 (temperature 230 ° C., load 2.16 kgf) is preferably 0.1 to 10 g / 10 min. More preferably, it is 5 to 6 g / 10 minutes, and further preferably 1 to 3 g / 10 minutes.

  The content of the compatibilizer (C) is 0 to 30 parts by mass, preferably 5 parts by mass or more, more preferably 10 parts by mass or more, with respect to 100 parts by mass of the polybutylene terephthalate resin (A). Preferably it is 15 mass parts or more, Preferably it is 25 mass parts or less, More preferably, it is 23 mass parts or less, More preferably, it is 20 mass parts or less. When the content is 5 parts by mass or more, layer peeling due to lack of compatibility tends to be suppressed, and when the content is 30 parts by mass or less, generation of gas tends to be suppressed.

[Reinforcing filler (D)]
The reinforcing filler (D) contained in the polyester resin composition of the present invention has the effect of improving the mechanical properties of the composition obtained by blending with the resin. Can be used. Preferably, a fibrous filler such as glass fiber, carbon fiber, basalt fiber, wollastonite, potassium titanate fiber is used. Of these, glass fibers are preferably used in view of mechanical strength, rigidity and heat resistance. In addition, granular or amorphous fillers such as calcium carbonate, titanium oxide, feldspar minerals, clays, organic clays, carbon black, glass beads; plate-like fillers such as talc; scales such as glass flakes, mica and graphite It is also preferable to use a filler in the form of dimensional stability.

  The content of the reinforcing filler (D) is 15 to 130 parts by mass, preferably 20 parts by mass or more, more preferably 30 parts by mass or more, with respect to 100 parts by mass of the polybutylene terephthalate resin (A). Is 120 parts by mass or less, more preferably 100 parts by mass or less. By setting the content to 15 parts by mass or more, the reinforcing effect of the obtained resin composition can be sufficiently exerted, and by setting the content to 130 parts by mass or less, while maintaining good fluidity, mechanical properties (particularly It is possible to increase impact resistance.

[Brominated flame retardant (E)]
The brominated flame retardant (E) contained in the polyester resin composition of the present invention includes brominated polycarbonate resin, brominated epoxy compound, brominated phenoxy resin, brominated polyphenylene ether resin, brominated polycarbonate oligomer, brominated polystyrene resin. Various bromine compounds such as brominated bisphenol A, glycidyl brominated bisphenol A, pentabromobenzyl polyacrylate, brominated imide (brominated phthalimide, etc.), brominated polystyrene, brominated epoxy compound, brominated aroma Group polycarbonate oligomers are preferred.

（式（１）中、ｔは１〜５の整数であり、ｎは繰り返し単位の数である。） Examples of the brominated polystyrene include brominated polystyrene containing a repeating unit represented by the following general formula (1).

(In formula (1), t is an integer of 1 to 5, and n is the number of repeating units.)

Brominated polystyrene may be either brominated polystyrene or produced by polymerizing brominated styrene monomers, but the polymerized brominated styrene is free bromine (atom) This is preferable because the amount is small.
In the general formula (1), the CH group to which brominated benzene is bonded may be substituted with a methyl group. The brominated polystyrene may be a copolymer obtained by copolymerizing another vinyl monomer. Examples of the vinyl monomer in this case include styrene, α-methylstyrene, acrylonitrile, methyl acrylate, butadiene, and vinyl acetate. Moreover, brominated polystyrene may be used as a single substance or a mixture of two or more different structures, and may contain units derived from styrene monomers having different numbers of bromines in a single molecular chain.

  Specific examples of brominated polystyrene include, for example, poly (4-bromostyrene), poly (2-bromostyrene), poly (3-bromostyrene), poly (2,4-dibromostyrene), poly (2,6 -Dibromostyrene), poly (2,5-dibromostyrene), poly (3,5-dibromostyrene), poly (2,4,6-tribromostyrene), poly (2,4,5-tribromostyrene) , Poly (2,3,5-tribromostyrene), poly (4-bromo-α-methylstyrene), poly (2,4-dibromo-α-methylstyrene), poly (2,5-dibromo-α- Methyl (styrene), poly (2,4,6-tribromo-α-methylstyrene), poly (2,4,5-tribromo-α-methylstyrene) and the like, and poly (2,4,6-tribromostyrene). And poly (2,4,5-tribromostyrene) and polydibromostyrene and polytribromostyrene containing an average of 2 to 3 bromine groups in the benzene ring are particularly preferably used.

In the brominated polystyrene, the number n (average polymerization degree) of the repeating units in the general formula (1) is preferably 30 to 1,500, more preferably 150 to 1,000, particularly 300 to 800. Is preferred. If the average degree of polymerization is less than 30, blooming tends to occur. On the other hand, if it exceeds 1,500, poor dispersion tends to occur and the mechanical properties tend to deteriorate. The mass average molecular weight (Mw) of brominated polystyrene is preferably 5,000 to 500,000, more preferably 10,000 to 500,000, and 10,000 to 300,000. More preferably, it is particularly preferably 30,000 to 80,000.
In particular, in the case of the brominated product of polystyrene described above, the mass average molecular weight (Mw) is preferably 50,000 to 70,000, and in the case of brominated polystyrene by a polymerization method, the mass average molecular weight (Mw) is 10 It is preferable that it is about 3,000-30,000. In addition, a mass average molecular weight (Mw) can be calculated | required as a value of standard polystyrene conversion by a gel permeation chromatography (GPC) measurement.

Moreover, as a brominated epoxy compound, the bisphenol A brominated epoxy compound represented by tetrabromobisphenol A epoxy is mentioned, for example.
The molecular weight of the brominated epoxy compound is not particularly limited. An oligomer may be used in combination as the brominated epoxy compound. When an oligomer is used in combination as the brominated epoxy compound, for example, by using about 0 to 50% by mass of an oligomer having a molecular weight of 5000 or less, flame retardancy, releasability and fluidity can be satisfied.

Furthermore, it is also preferable to use a brominated aromatic polycarbonate oligomer as the brominated flame retardant (E) used in the present invention from the viewpoint of dispersibility in the aromatic polycarbonate resin (C). Among them, a brominated aromatic polycarbonate oligomer obtained by reacting (condensation polymerization) tetrabromobisphenol A (sometimes abbreviated as “TBA”) with phosgene or a carbonic acid diester using an appropriate molecular weight regulator. Is particularly preferred. Further, it may be a copolymer type in which a part of tetrabromobisphenol A is substituted with another dihydric phenol, and the dihydric phenol described in the above aromatic polycarbonate resin is used as the other dihydric phenol. Furthermore, bisphenol A (sometimes abbreviated as “BPA”) is preferable from the viewpoint of yield during synthesis, ease of solidification, and high versatility (price).
When such a brominated aromatic polycarbonate oligomer has a degree of polymerization of 1, it tends to bleed out from the molded product at the time of molding, and on the other hand, when the degree of polymerization increases, it becomes difficult to obtain satisfactory fluidity. The preferred degree of polymerization is 2-15.

Brominated aromatic polycarbonate oligomers that satisfy these requirements are commercially available and can be easily obtained. For example, an oligomer (average degree of polymerization of 5) obtained by reacting TBA and phosgene using 2,4,6-tribromophenol (sometimes abbreviated as “TBPH”) as a molecular weight regulator is Mitsubishi Engineering. It is commercially available from Plastics Co., Ltd. under the trade name: Iupilon FR-53.
The brominated aromatic polycarbonate oligomer may be used alone or in combination of two or more. Moreover, unless the characteristic of this invention is impaired, other brominated flame retardants other than brominated aromatic polycarbonate oligomer can also be used together.

The brominated flame retardant (E) preferably has a bromine concentration of 52 to 75% by mass, more preferably 56 to 73% by mass, and even more preferably 57 to 72% by mass. By setting the bromine concentration in such a range, it is easy to keep good flame retardancy.
The content of free bromine in the brominated flame retardant (E) is preferably 0.5% by mass or less, more preferably 0.45% by mass or less, and 0.4% by mass or less. More preferably it is. When the content of free bromine exceeds 0.5% by mass, the amount of free bromine in the resin composition finally obtained increases, and is desorbed when the resin composition is at a high temperature during processing or molding. In some cases, the heat discoloration resistance, color tone, and light discoloration stability of the resin composition may be deteriorated, or metal corrosion of a mold or the like may be caused during molding. Also, removing the free bromine content up to 0% by mass requires purification so as not to be economical, so the lower limit of the content is usually 0.001% by mass and 0.005% by mass. %, And more preferably 0.01% by mass.

  Further, the chlorine content in the brominated flame retardant (E) is preferably 0.2% by mass or less, more preferably 0.15% by mass or less, and 0.08% by mass or less. More preferably, it is especially preferable that it is 0.03 mass% or less. When the content of chlorine in the brominated flame retardant (E) exceeds 0.2% by mass, the chlorine content in the resin composition finally obtained tends to be too large, and the tracking resistance and toughness tend to deteriorate. It is in.

  Furthermore, the sulfur content in the brominated flame retardant (E) is preferably 0.1% by mass or less, more preferably 0.05% by mass or less, and 0.02% by mass or less. More preferably. If the sulfur content in the brominated flame retardant (E) exceeds 0.1% by mass, the sulfur content in the finally obtained resin composition will increase too much, resulting in tracking resistance and mold corrosion resistance. Tend to get worse.

  The content of free bromine, chlorine and sulfur in the brominated flame retardant (E) can be measured by a combustion ion chromatography method. Specifically, it was generated by heating a brominated flame retardant (E) under conditions of 270 ° C. and 10 minutes in an argon atmosphere using an automatic sample combustion apparatus of “AQF-100 type” manufactured by Mitsubishi Chemical Analytech Co., Ltd. The amount of bromine, chlorine and sulfur can be determined by quantifying using “ICS-90” manufactured by Nippon Dionex.

  Content of a brominated flame retardant (E) is 10-45 mass parts with respect to 100 mass parts of polybutylene terephthalate resins. When the content is less than 10 parts by mass, a sufficient flame retarding effect cannot be obtained, and when it exceeds 45 parts by mass, the mechanical strength is lowered. The preferred content of the brominated flame retardant (E) is 15 parts by mass or more, more preferably 18 parts by mass or more, further preferably 20 parts by mass or more, with respect to 100 parts by mass of the polybutylene terephthalate resin. Preferably it is 40 mass parts or less, More preferably, it is 35 mass parts or less, More preferably, it is 30 mass parts or less.

[Antimony flame retardant aid (F)]
Examples of the antimony flame retardant aid (F) contained in the polyester resin composition of the present invention include antimony trioxide (Sb ₂ O ₃ ), antimony pentoxide (Sb ₂ O ₅ ), and sodium antimonate. Antimony pentoxide tends to cause a drop in impact resistance, and antimony trioxide is particularly preferable.
The content of the antimony flame retardant auxiliary (F) is 3 to 30 parts by mass, more preferably 5 parts by mass or more, and further 6 parts by mass or more with respect to 100 parts by mass of the thermoplastic polyester resin (A). It is preferably 20 parts by mass or less, more preferably 15 parts by mass or less. When the content is less than 3 parts by mass, the flame retardancy is reduced, and when it exceeds 30 parts by mass, mechanical properties such as impact resistance are reduced.

  The mass concentration of the bromine atom derived from the brominated flame retardant (E) and the antimony atom derived from the antimony flame retardant auxiliary compound (F) in the polyester resin composition is usually 3 to 25% by mass in total. It is preferably 4 to 22% by mass, more preferably 5 to 16% by mass, and further preferably 6 to 15% by mass. If it is less than 3% by mass, the flame retardancy tends to decrease, and if it exceeds 25% by mass, the mechanical strength and tracking resistance may decrease. The mass ratio (Br / Sb) of bromine atoms and antimony atoms is preferably 0.3 to 5, and more preferably 0.3 to 4.

[Acrylonitrile-styrene resin (G)]
The polyester resin composition of the present invention further contains acrylonitrile-styrene resin (G). By containing the acrylonitrile-styrene resin (G), the dispersibility of the carbon black (H) is improved.
The acrylonitrile-styrene-based resin (G) is not particularly limited, but the ratio of acrylonitrile to styrene is preferably in the range of acrylonitrile / styrene = 20/80 to 45/55 by mass ratio, and in the range of 25/75 to 35/65. Is more preferable. Although it does not restrict | limit especially as a manufacturing method of an acrylonitrile styrene-type resin, Suspension polymerization, emulsion polymerization, solution polymerization, bulk polymerization, etc. are mentioned. The molecular weight of the acrylonitrile-styrene-based resin (G) is not particularly limited, but is preferably in the range of 50,000 to 200,000 (polystyrene conversion) in terms of mass average molecular weight measured by gel permeation chromatography using tetrahydrofuran as a solvent.

  Moreover, the acrylonitrile-styrene resin (G) may contain an epoxy group. Although it does not restrict | limit especially as an epoxy-group containing acrylonitrile-styrene-type resin, For example, 15-40 mass% of vinyl cyanide monomer units, 60-84.9 mass% of aromatic vinyl monomer units, and an epoxy group containing A copolymer resin composed of 0.1 to 0.4% by mass of vinyl monomer units is preferred. Although it does not restrict | limit especially as a manufacturing method of an epoxy-group-containing acrylonitrile-styrene-type resin, Suspension polymerization, emulsion polymerization, solution polymerization, bulk polymerization, etc. are mentioned.

  The content of the acrylonitrile-styrene resin (G) is preferably 0.1 to 5 parts by mass, more preferably 0.3 parts by mass or more, more preferably 100 parts by mass of the polybutylene terephthalate resin (A). Is 0.6 parts by mass or more, preferably 3 parts by mass or less, more preferably 2 parts by mass or less. When the content of the acrylonitrile-styrene resin (G) is in such a range, the dispersibility of the carbon black (H) is improved.

[Carbon black (H)]
The polyester resin composition of the present invention preferably further contains carbon black (H). By containing carbon black (H), weather resistance as a wattmeter exterior material is improved.
Carbon black (H) used in the present invention is not limited in type, raw material type, and production method, and any of furnace black, channel black, acetylene black, ketjen black, and the like can be used. The number average particle diameter is not particularly limited, but is preferably 5 to 60 nm. As described above, by using carbon black having a number average particle diameter in a predetermined range, a composition in which blisters are hardly generated at a high temperature can be obtained. In addition, the number average particle diameter is obtained as a unit constituent particle from an aggregate enlarged image obtained by the procedure described in ASTM D3849 standard (standard test method of carbon black—morphological characterization by electron microscopy). 3,000 particle diameters can be measured and arithmetically averaged.

Nitrogen adsorption specific surface area of the carbon black (H) ^{(Unit: m} 2 / g) is preferably usually less than 1000 m ² / g, is preferably Among them 50 to 400 m ² / g. By making the nitrogen adsorption specific surface area less than 1000 m ² / g, the flowability of the polycarbonate resin composition of the present invention and the appearance of the molded product tend to be improved, which is preferable. The nitrogen adsorption specific surface area can be measured according to JIS K6217.

The DBP (dibutyl phthalate) absorption amount of carbon black (H) ^is preferably less than 300 cm 3/100 g, is preferably Among them 30~200cm ³ / 100g. The DBP absorption amount by less than 300 cm ^3/100 g, preferably tends to increase the appearance of fluidity and a molded article of the polycarbonate resin composition of the present invention.
Incidentally, DBP absorption ^(unit: cm 3 / 100g) can be measured according to JIS K6217. The carbon black used in the present invention is not particularly limited with respect to its pH, but it is usually 2 to 10, preferably 3 to 9, and more preferably 4 to 8.

  Carbon black (H) can be used alone or in combination of two or more. Furthermore, carbon black can be granulated using a binder, and can also be used in a masterbatch that is melt-kneaded at a high concentration in another resin. By using the melt-kneaded master batch, the handling property during extrusion and the dispersibility improvement in the resin composition can be achieved. Examples of the resin include polystyrene-based resins, polycarbonate-based resins, acrylic resins, and the like. In particular, the above-described acrylonitrile-styrene-based resin (G) is preferably used.

  In the present invention, when carbon black (H) is previously masterbatched with acrylonitrile-styrene resin (G), the acrylonitrile-styrene resin (G) has a mass average molecular weight of 200,000 or less. Is preferred. A conventionally known method such as melt-kneading can be adopted as a method for masterbatch formation. Moreover, it is preferable that content of carbon black (H) in a masterbatch is 10-80 mass%, 20-70 mass% is more preferable, 30-60 mass% is further more preferable. If the carbon black content in the masterbatch exceeds 80% by mass, poor dispersion of the carbon black may occur, which is not preferable. Further, the amount of carbon black masterbatch used may be appropriately selected and determined, but is usually 1 to 10 parts by mass with respect to 100 parts by mass of polybutylene terephthalate resin (A), and in particular 2 to 8 parts by mass. Preferably there is. In the resin composition of the present invention, the acrylonitrile used for the carbon black masterbatch so that the acrylonitrile-styrene resin (G) is 0.1 to 5 parts by mass with respect to 100 parts by mass of the polybutylene terephthalate resin (A). -What is necessary is just to adjust the quantity of a styrene-type resin (G).

  The content of carbon black (H) is 0.001 to 3 parts by mass, preferably 0.01 parts by mass or more, and more preferably 0.1 parts by mass with respect to 100 parts by mass of the polycarbonate resin (A). As mentioned above, it is 0.3 mass part or more especially, Preferably it is 2.5 mass parts or less, More preferably, it is 2 mass parts or less, Most preferably, it is 1.5 mass parts or less. When the content is less than 0.001 part by mass, the weather resistance is insufficient, and when it exceeds 3 parts by mass, mechanical properties such as moldability and impact resistance are deteriorated.

[Stabilizer]
It is preferable that the polyester resin composition of the present invention further contains a stabilizer because it has effects of improving thermal stability and preventing deterioration of mechanical strength, transparency and hue. As the stabilizer, a phosphorus stabilizer and a phenol stabilizer are preferable.
In particular, when a phosphorus stabilizer is contained, the transesterification reaction between the polybutylene terephthalate resin (A) and the compatibilizer (C) blended as necessary is suppressed, and the polybutylene terephthalate resin (A) and the bromine-based difficult agent are suppressed. The mutual compatibility of the flame retardant (E) and the compatibilizing agent (C) can be remarkably improved, and, surprisingly, excellent extensibility can be expressed even in a thin molded article.

  Examples of the phosphorus-based stabilizer include phosphorous acid, phosphoric acid, phosphite ester, and phosphate ester. Among them, organic phosphate compounds, organic phosphite compounds, and organic phosphonite compounds are preferable.

The organic phosphate compound is preferably the following general formula:
(R ¹ O) _3-n P (═O) OH _n
(In the formula, R ¹ is an alkyl group or an aryl group, and may be the same or different. N represents an integer of 0 to 2.)
It is a compound represented by these. More preferably, R ¹ is a long-chain alkyl acid phosphate compound having 8 to 30 carbon atoms. Specific examples of the alkyl group having 8 to 30 carbon atoms include octyl group, 2-ethylhexyl group, isooctyl group, nonyl group, isononyl group, decyl group, isodecyl group, dodecyl group, tridecyl group, isotridecyl group, tetradecyl group, A hexadecyl group, an octadecyl group, an eicosyl group, a triacontyl group, etc. are mentioned.

Examples of the long-chain alkyl acid phosphate include octyl acid phosphate, 2-ethylhexyl acid phosphate, decyl acid phosphate, lauryl acid phosphate, octadecyl acid phosphate, oleyl acid phosphate, behenyl acid phosphate, phenyl acid phosphate, nonyl phenyl acid phosphate Acid phosphate, phenoxyethyl acid phosphate, alkoxy polyethylene glycol acid phosphate, bisphenol A acid phosphate, dimethyl acid phosphate, diethyl acid phosphate, dipropyl acid phosphate, diisopropyl acid phosphate, dibutyl acid phosphate, geo Chill acid phosphate, di-2-ethylhexyl acid phosphate, dioctyl acid phosphate, dilauryl acid phosphate, distearyl acid phosphate, diphenyl acid phosphate, and a bis-nonylphenyl acid phosphate, or the like.
Among these, octadecyl acid phosphate is preferable, and this is marketed under the trade name “ADEKA STAB AX-71” of ADEKA.

As the organic phosphite compound, preferably, the following general formula:
^{R 2 O-P (OR 3} ) (OR 4)
Wherein R ² , R ³ and R ⁴ are each a hydrogen atom, an alkyl group having 1 to 30 carbon atoms or an aryl group having 6 to 30 carbon atoms, and at least one of R ² , R ³ and R ⁴ One is an aryl group having 6 to 30 carbon atoms.)
The compound represented by these is mentioned.

  Examples of the organic phosphite compound include triphenyl phosphite, tris (nonylphenyl) phosphite, dilauryl hydrogen phosphite, triethyl phosphite, tridecyl phosphite, tris (2-ethylhexyl) phosphite, and tris (tridecyl). ) Phosphite, tristearyl phosphite, diphenyl monodecyl phosphite, monophenyl didecyl phosphite, diphenyl mono (tridecyl) phosphite, tetraphenyldipropylene glycol diphosphite, tetraphenyltetra (tridecyl) pentaerythritol tetraphosphite Hydrogenated bisphenol A phenol phosphite polymer, diphenyl hydrogen phosphite, 4,4′-butylidene-bis (3-methyl-6-t rt-butylphenyldi (tridecyl) phosphite), tetra (tridecyl) 4,4′-isopropylidenediphenyldiphosphite, bis (tridecyl) pentaerythritol diphosphite, bis (nonylphenyl) pentaerythritol diphosphite, di Lauryl pentaerythritol diphosphite, distearyl pentaerythritol diphosphite, tris (4-tert-butylphenyl) phosphite, tris (2,4-di-tert-butylphenyl) phosphite, hydrogenated bisphenol A pentaerythritol phosphite Phytopolymer, bis (2,4-di-tert-butylphenyl) pentaerythritol diphosphite, bis (2,6-di-tert-butyl-4-methylphenyl) pentaerythritol diphosphite Phosphite, 2,2'-methylenebis (4,6-di -tert- butylphenyl) octyl phosphite, bis (2,4-dicumylphenyl) pentaerythritol diphosphite and the like.

The organic phosphonite compound is preferably the following general formula:
R ⁵ -P (OR ⁶ ) (OR ⁷ )
(Wherein R ⁵ , R ⁶ and R ⁷ are each a hydrogen atom, an alkyl group having 1 to 30 carbon atoms or an aryl group having 6 to 30 carbon atoms, and at least one of R ⁵ , R ⁶ and R ⁷ ) One is an aryl group having 6 to 30 carbon atoms.)
The compound represented by these is mentioned.

  Examples of the organic phosphonite compound include tetrakis (2,4-di-iso-propylphenyl) -4,4′-biphenylenediphosphonite, tetrakis (2,4-di-n-butylphenyl) -4,4′-biphenyl. Range phosphonite, tetrakis (2,4-di-tert-butylphenyl) -4,4'-biphenylene diphosphonite, tetrakis (2,4-di-tert-butylphenyl) -4,3'-biphenylene diphospho Knight, tetrakis (2,4-di-tert-butylphenyl) -3,3'-biphenylenediphosphonite, tetrakis (2,6-di-iso-propylphenyl) -4,4'-biphenylenediphosphonite, Tetrakis (2,6-di-n-butylphenyl) -4,4′-biphenylenediphosphonite, tetrakis (2, -Di-tert-butylphenyl) -4,4'-biphenylenediphosphonite, tetrakis (2,6-di-tert-butylphenyl) -4,3'-biphenylenediphosphonite, and tetrakis (2,6- And di-tert-butylphenyl) -3,3′-biphenylenediphosphonite.

One type of phosphorous stabilizer may be contained, or two or more types may be contained in any combination and ratio.
As described above, octadecyl acid phosphate that exhibits excellent compatibility and dramatically improves elongation and thin wall toughness in combination with the aromatic polycarbonate resin (C) is particularly preferable as the phosphorus stabilizer.

  Examples of the phenol-based stabilizer include pentaerythritol tetrakis (3- (3,5-di-tert-butyl-4-hydroxyphenyl) propionate), octadecyl-3- (3,5-di-tert-butyl-4) -Hydroxyphenyl) propionate, thiodiethylenebis (3- (3,5-di-tert-butyl-4-hydroxyphenyl) propionate), pentaerythritol tetrakis (3- (3,5-di-neopentyl-4-hydroxyphenyl) ) Propionate) and the like. Among these, pentaerythritol tetrakis (3- (3,5-di-tert-butyl-4-hydroxyphenyl) propionate), octadecyl-3- (3,5-di-tert-butyl-4-hydroxyphenyl) ) Propionate is preferred.

  Content of a stabilizer is 0.001-1 mass part normally with respect to 100 mass parts of polybutylene terephthalate resins (A). When the content of the stabilizer is less than 0.001 part by mass, it is difficult to expect an improvement in the thermal stability and compatibility of the resin composition, and a decrease in molecular weight and a deterioration in hue during molding are likely to occur. When it exceeds, it will become excess amount and there exists a tendency for generation | occurrence | production of silver and a hue deterioration to occur further easily. The content of the stabilizer is more preferably 0.001 to 0.7 parts by mass, and still more preferably 0.005 to 0.5 parts by mass.

[Other flame retardants]
The polyester resin composition of the present invention can also contain a flame retardant other than the brominated flame retardant (E).
As a flame retardant other than the brominated flame retardant (E), a phosphorus flame retardant and a silicone flame retardant can be contained, and a phosphorus flame retardant is preferably contained.

  Examples of the phosphorus-based flame retardant include (di) phosphinic acid metal salts such as aluminum ethylphosphinate, aluminum diethylphosphinate, aluminum ethylmethylphosphinate, zinc diethylphosphinate, and melamine and phosphorus represented by melamine polyphosphate. Reaction products with acids, phosphate esters, phosphazenes, etc. are mentioned. Among them, phosphazenes such as metal salts of diethylphosphinic acid, melamine polyphosphate, cyclic phenoxyphosphazene, chain phenoxyphosphazene, and crosslinked phenoxyphosphazene have excellent thermal stability It is preferable from the point.

[Anti-drip agent]
It is also preferable that the polyester resin composition of the present invention contains an anti-dripping agent. As the anti-drip agent, polytetrafluoroethylene (PTFE) is preferable, has a fibril-forming ability, easily disperses in the resin composition, and shows a tendency to form a fibrous material by bonding the resins together. is there. Specific examples of polytetrafluoroethylene include, for example, trade names “Teflon (registered trademark) 6J” or “Teflon (registered trademark) 30J” commercially available from Mitsui DuPont Fluorochemical Co., Ltd., Daikin Industries, Ltd. Examples thereof include a commercially available product name “Polyflon (registered trademark)” and a product name “Fullon (registered trademark)” marketed by Asahi Glass Co., Ltd.
The content ratio of polytetrafluoroethylene is preferably 0.1 to 20 parts by mass with respect to 100 parts by mass of the polybutylene terephthalate resin (A). If the polytetrafluoroethylene having fibril forming ability is less than 0.1 parts by mass, the flame retardancy tends to be insufficient, and if it exceeds 20 parts by mass, the appearance tends to deteriorate. The content ratio of polytetrafluoroethylene is more preferably 0.3 to 10 parts by mass with respect to 100 parts by mass of the polybutylene terephthalate resin (A).

[Release agent]
The polyester resin composition of the present invention preferably further contains a release agent. As the mold release agent, known mold release agents usually used for polyester resins can be used. Among them, polyolefin compounds, fatty acid ester compounds, and silicone systems are particularly difficult in that they do not hinder metal film adhesion. One or more mold release agents selected from compounds are preferred.

  Examples of the polyolefin compound include compounds selected from paraffin wax and polyethylene wax. Among them, those having a mass average molecular weight of 700 to 10,000, more preferably 900 to 8,000 are preferable.

  Examples of the fatty acid ester compounds include fatty acid esters such as glycerin fatty acid esters and sorbitan fatty acid esters, and partially saponified products thereof. Among them, the fatty acid ester compounds are composed of fatty acids having 11 to 28 carbon atoms, preferably 17 to 21 carbon atoms. Preferred are mono- or di-fatty acid esters. Specifically, glycerol monostearate, glycerol monobehenate, glycerol dibehenate, glycerol-12-hydroxy monostearate, sorbitan monobehenate, etc. are mentioned.

  Moreover, as a silicone type compound, the compound modified | denatured from points, such as compatibility with a polyester resin, is preferable. Examples of the modified silicone oil include silicone oil in which an organic group is introduced into the side chain of polysiloxane, silicone oil in which an organic group is introduced into both ends and / or one end of polysiloxane, and the like. Examples of the organic group to be introduced include an epoxy group, an amino group, a carboxyl group, a carbinol group, a methacryl group, a mercapto group, and a phenol group, and preferably an epoxy group. As the modified silicone oil, a silicone oil in which an epoxy group is introduced into the side chain of polysiloxane is particularly preferable.

  It is preferable that content of a mold release agent is 0.05-2 mass parts with respect to 100 mass parts of polybutylene terephthalate resin (A). If the amount is less than 0.05 parts by mass, the surface property tends to decrease due to defective mold release at the time of melt molding. On the other hand, if it exceeds 2 parts by mass, the kneading workability of the resin composition decreases, and molding is also performed. The surface of the product may be cloudy. The content of the release agent is preferably 0.07 to 1.5 parts by mass, more preferably 0.1 to 1.0 parts by mass.

[Other ingredients]
The polyester resin composition of the present invention may further contain various additives as long as the effects of the present invention are not impaired. Examples of such additives include ultraviolet absorbers, dyes and pigments, fluorescent whitening agents, antistatic agents, antifogging agents, lubricants, antiblocking agents, fluidity improvers, plasticizers, dispersants, antibacterial agents, and the like. It is done.

  Moreover, the polyester resin composition in the present invention can contain a thermoplastic resin other than the polybutylene terephthalate resin and the compatibilizer within a range not impairing the effects of the present invention. Specific examples of other thermoplastic resins include polyacetal resins, polyamide resins, polyphenylene oxide resins, polystyrene resins, polyphenylene sulfide resins, polysulfone resins, polyether sulfone resins, polyetherimide resins, and polyether ketone resins. And polyolefin resins.

[Method for Producing Resin Composition]
As a manufacturing method of the polyester resin composition of this invention, it can carry out in accordance with the conventional method of thermoplastic polyester resin composition preparation. Usually, the components and various additives added as desired are mixed together and then melt-kneaded in a single-screw or twin-screw extruder. Also, the resin composition of the present invention can be prepared by mixing each component in advance or by mixing only a part of the components in advance and supplying them to an extruder using a feeder and melt-kneading them. Further, a master batch is prepared by melting and kneading a part of a polyester resin and a part of other components, and then the remaining polyester resin and other ingredients are blended and melt kneaded. Good.
In addition, when using fibrous things, such as glass fiber, as an inorganic filler, it is also preferable to supply from the side feeder in the middle of the cylinder of an extruder.

  The heating temperature at the time of melt kneading can be appropriately selected from the range of usually 220 to 300 ° C. If the temperature is too high, decomposition gas is likely to be generated, which may cause opacity. Therefore, it is desirable to select a screw configuration in consideration of shear heat generation. In order to suppress decomposition during kneading or molding in the subsequent process, it is desirable to use an antioxidant or a heat stabilizer.

[Power meter exterior molding]
The polyester resin composition of the present invention is used as a molded body for wattmeter exterior. Examples of the molded body for the wattmeter exterior include a wattmeter cover, a housing, and a casing.
The manufacturing method of a molded object is not specifically limited, The molding method generally employ | adopted about the polyester resin composition can be employ | adopted arbitrarily. For example, injection molding method, ultra-high speed injection molding method, injection compression molding method, two-color molding method, hollow molding method such as gas assist, molding method using heat insulating mold, rapid heating mold were used. Molding method, foam molding (including supercritical fluid), insert molding, IMC (in-mold coating molding) molding method, extrusion molding method, sheet molding method, thermoforming method, rotational molding method, laminate molding method, press molding method, Examples thereof include a blow molding method. Among these, it is preferable to use an injection molding method.

Hereinafter, the present invention will be described more specifically with reference to examples. However, the present invention is not construed as being limited to the following examples.
In the following description, “parts” means “parts by mass” based on mass standards unless otherwise specified.
In the following Examples and Comparative Examples, the components used are as shown in Table 1 below.

(Examples 1-9, Comparative Examples 1-3)
Each component described in Table 1 below was blended so as to have a blending ratio (parts by mass) described in Table 2 and Table 3, and a twin-screw extruder (“TEX-30α” manufactured by Nippon Steel Works, L / D = 52), pellets of an extruded resin composition were produced at a barrel set temperature of 250 ° C. and a rotation speed of 200 rpm. The characteristics of the obtained pellets were evaluated for test pieces that were injection molded at a cylinder temperature of 250 ° C. and a mold temperature of 80 ° C. using an injection molding machine (Nex80-9E manufactured by Nissei Plastic Industry Co., Ltd.). In molding, the resin composition was dried at 120 ° C. for 6 to 8 hours until immediately before the molding.

<Evaluation method>
Each evaluation method is as follows.
(1) Flame Retardancy Combustion test pieces with a size of 125 x 12.5 mm x 1.6 mmt are molded and allowed to stand for 48 hours or more at 23 ° C ± 2 ° C and humidity of 50% ± 5%. The flame retardancy was evaluated in conformity.
(2) Low warpage A box-shaped molded product (wall thickness: 1.5 mmt) having a size of 150 × 80 × 40 mm was molded, and the degree of internal warpage of the long side was measured with a gap gauge. It can be said that the smaller the degree of inner curvature, the better the dimensional stability.

(3) Tensile strength The ISO test pieces before and after the hydrolysis resistance test, heat aging test, and weather resistance test were measured under conditions of a tensile speed of 5 mm / min according to the ISO527 standard.
(4) Degree of fading About the ISO test piece after a heat aging test and a weather resistance test, the black fading degree was visually observed. The case where there was almost no change in blackness was evaluated as “◯”, the case where the blackness remained slightly “△”, and the case where the color changed to brown was evaluated as “X”.
(5) Appearance A box-shaped molded product (wall thickness: 1.5 mmt) having a size of 150 × 80 × 40 mm was formed, and the appearance was visually observed. The case where the glass fiber was hardly lifted was evaluated as “◯”, the case where the glass fiber was slightly conspicuous was evaluated as “Δ”, and the case where the glass fiber was conspicuous was evaluated as “x”.

(6) Surface impact (falling ball impact test)
A box-shaped molded product with a size of 150 x 80 x 40 mm (thickness 1.5 mmt) is molded, and a 2.975 kg steel ball is dropped from a predetermined height, and the height at which the molded product is completely destroyed is obtained. It was. It can be said that the higher the height at the time of complete destruction, the better the surface impact.
(7) Hydrolysis resistance test The ISO test piece was left in a pressure cooker tester at a temperature of 121 ° C, a humidity of 100%, and a pressure of 2 atm for 50 hours.

(8) Heat aging resistance test The ISO test piece was left in a hot air oven at a temperature of 150 ° C for 500 hours.
(9) Weather resistance test The ISO test piece was processed under the following conditions using a xenon weather tester.
Equipment used: Atlas Ci4000
Filter / Inner; Quartz Filter / Outer; Type S borosilicate Black panel temperature; 63 ° C
Irradiance: 0.55 W / m ² (at 340 nm)
Treatment time: 1000 hours Water spray time; 18 minutes Water spray stop time; 120 minutes Humidity; 50% (95% during rain)
The above evaluation results are shown in Table 2 and Table 3 below.

  From Table 2 and Table 3, it can be seen that the polyester resin composition of the present invention is excellent in all of heat aging resistance, low warpage, hydrolysis resistance, flame resistance, weather resistance, and appearance.

  The polyester resin composition of the present invention is excellent in impact resistance, heat resistance, heat aging resistance, low warpage, hydrolysis resistance, flame resistance, weather resistance, appearance, and the like. Therefore, since the polyester resin composition of the present invention can be suitably applied as a molded product for wattmeter exteriors, the industrial utility is very high.

Claims (5)

  20-100 parts by mass of styrene-based copolymer (B), 0-30 parts by mass of compatibilizer (C), 15-130 parts by mass of reinforcing filler (D) with respect to 100 parts by mass of polybutylene terephthalate resin (A). Bromine flame retardant (E) 10 to 45 parts by mass, antimony flame retardant auxiliary (F) 3 to 30 parts by mass, acrylonitrile-styrene resin (G) 0.1 to 5 parts by mass and carbon black (H) 0 0.001 to 3 parts by mass of a polyester resin composition for exterior wattmeters.   The polyester resin composition for exterior wattmeters according to claim 1, wherein the content of the compatibilizer (C) is 5 to 25 parts by mass with respect to 100 parts by mass of the polybutylene terephthalate resin (A).   The polyester resin composition for exterior wattmeters according to claim 1 or 2, wherein the compatibilizing agent (C) is an aromatic polycarbonate resin.   The polyester resin composition for wattmeter exterior according to any one of claims 1 to 3, wherein the aromatic polycarbonate resin has a viscosity average molecular weight (Mv) of 23,000 to 35,000.   The bromine-based flame retardant (E) is pentabromobenzyl polyacrylate, brominated polystyrene, brominated epoxy compound, or brominated aromatic polycarbonate oligomer, The polyester resin composition for wattmeter exterior according to any one of claims 1 to 4. .