JPH1024437A - Manufacture of molded product of fire-retardant thermoplastic resin composition - Google Patents

Abstract

PROBLEM TO BE SOLVED: To make the appearance, thermal discoloration and mechanical physical properties, especially, impact resistance of a molded product excellent because a fire retardant is uniformly dispersed in a resin, the irregularity of fire retardancy and physical properties is extremely reduced and the addition amt. of a heat stabilizer is supressed low by the reduction of heat history. SOLUTION: A granaular fire retardant compsn. 2-45 pts.wt. consisting of two or more components selected from a fire retardant (B), a fire retardant aid (C) and a heat stabilizer (D) and containing one or more component becoming a binder at a time of granulation among the components (B), (C), (D) and not substantially containing a component other than those is mixed with 100 pts.wt. of a thermoplastic resin (A) and these components are melted and kneaded in an injection molding machine and the resulting molten matter is injected into a mold to be cooled.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

BACKGROUND OF THE INVENTION The present invention relates to a flame retardant which is uniformly dispersed in a resin, has very little variation in flame retardancy and physical properties, and can reduce the amount of a heat stabilizer to be added due to a decrease in heat history. The present invention relates to a method for producing a molded article of a flame-retardant thermoplastic resin composition capable of giving a molded article excellent in appearance, thermal discoloration, and mechanical properties, particularly impact resistance, of the molded article.

[0002]

2. Description of the Related Art In general, in order to obtain a molded article made of a flame-retardant thermoplastic resin, first, a thermoplastic resin and various flame retardants are melt-kneaded, pellets of the flame-retardant resin are produced, and then an injection molding machine is used. The product of the flame-retardant resin was obtained using such as. However, this method gives the resin a thermal history of several degrees, and thus easily causes thermal deterioration and thermal discoloration. In order to suppress this, it has been essential to add a heat stabilizer and an antioxidant. However, the impact resistance is significantly reduced by these additives,
Further, there is a problem that the appearance of the molded article is apt to be deteriorated due to the thermal decomposition.

On the other hand, when a thermoplastic resin and a flame retardant are directly molded by a molding machine without performing preliminary kneading, the flame retardant is mostly in a powdery or liquid state. There was a problem with sex. When the flame retardant is in the form of powder, dust is liable to be scattered at the time of compounding, so that not only the workability is poor but also the working environment is not preferable. In addition, non-uniform mixing may occur due to classification at the time of mixing with the thermoplastic resin. When the flame retardant is in a liquid state, special equipment such as a feeder for liquid addition is required in order to improve the quantitativeness.

As means for solving these disadvantages, for example, Japanese Patent Publication No. 4-28740 discloses a particulate flame retardant comprising a flame retardant and a thermoplastic resin.
Japanese Patent Application Laid-Open Publication No. H11-163873 discloses a flame retardant masterbatch for a thermoplastic resin comprising a resin-based flame retardant (A) which melts at a molding temperature of a thermoplastic resin to be flame-retarded and a flame retardant (B) which does not melt at the molding temperature. Is described. However, since these flame retardant masterbatches contain a thermoplastic resin as a binder, in consideration of the dispersibility of the flame retardant and the physical properties of the flame retardant resin composition, the thermoplastic resin that becomes the binder according to the resin to be blended is used. It is necessary to select the composition and molecular weight of the resin. As a result, a large number of flame retardant master batches are required, and the management becomes very complicated. Furthermore, although this flame-retardant masterbatch is excellent in powdering resistance, since the flame-retardant is firmly hardened by the resin, it is often difficult to uniformly disperse the flame-retardant in the resin when performing melt-kneading. There was a problem that.
JP-A-55-21439 discloses a method of obtaining a particulate flame retardant by mixing a halogen compound, an inorganic flame retardant and other inorganic compounds by a wet method, molding and drying. ing. However, in this method, when a solvent is used during wet mixing, it is difficult to obtain a composition having a uniform particle diameter because the particulate flame retardants are easily re-fused with each other in the drying step. Has poor powdering resistance. Furthermore, JP-A-6-256563 describes a particulate flame retardant containing an inorganic flame retardant containing antimony oxide as an essential component, a fatty acid amide and a lubricant having a lower melting point than the fatty acid amide. However, this particulate flame retardant contains a fatty acid amide and a lubricant having a lower melting point than that of the particulate flame retardant.
It is not preferable for use in the standard V-0. Also, the melting points of the fatty acid amide and the lubricant are lower than the molding temperature of the thermoplastic resin,
It has a drawback that it tends to cause poor dispersion due to fusion to the screw below the hopper during molding.

[0005]

As described above, when pre-kneading is performed, a large amount of a heat stabilizer and an antioxidant must be added to some extent, and therefore, mechanical properties, particularly, impact resistance are poor. In some cases, due to these thermal decompositions, the appearance of the molded article becomes inferior. On the other hand, without preliminary kneading, it is difficult to obtain a composition having a uniform composition.

[0006] Even with the conventional technique of granulating various flame retardants to make them easy to handle, the management is complicated because the resin to be blended is limited, and there is a problem in the dispersibility of the flame retardants. When used in a method of obtaining a molded product by directly mixing with a thermoplastic resin and performing injection molding, there was a problem that satisfactory physical properties and flame retardancy could not be obtained, or that the product was varied. . The present invention provides a method for producing a molded article of a flame-retardant resin composition in which a flame retardant is uniformly dispersed under these circumstances, and there is no variation in physical properties or flame retardancy, and excellent mechanical properties, especially impact resistance. The purpose is to provide.

[0007]

As a result of intensive studies, the present inventors have selected a component selected from a flame retardant, a flame retardant aid, and a heat stabilizer as a binder, and substantially contained components other than these. By not allowing it to be transported, mixed, and kept in a granular form when it is supplied to the molding machine, it is immediately crushed or melted during melt-kneading in the injection molding machine, and the flame retardant, flame retardant auxiliary, and heat stabilizer are added to the resin. The use of a particulate flame retardant composition that can be uniformly dispersed in a liquid does not require pre-kneading, and thus minimizes the use of heat stabilizers. The inventors have invented a method for producing a molded article of a flame-retardant thermoplastic resin composition having excellent impact properties.

[0008] That is, the present invention relates to a thermoplastic resin (A) 1
Flame retardant (B), flame retardant auxiliary (C),
Consisting of two or more components selected from heat stabilizers (D),
At least one of the components (B), (C) and (D) is selected from binders, and the particulate flame retardant composition (E) contains substantially no other components. )
After mixing 2 to 45 parts by weight, the mixture is melt-kneaded in an injection molding machine, and the melt is injected into a mold and cooled, thereby producing a molded article of a flame-retardant thermoplastic resin composition. About.

The thermoplastic resin (A) in the present invention includes, for example, homopolymers, copolymers and rubber-reinforced types thereof. Specifically, polystyrene,
Styrene-acrylonitrile copolymer, polymers and copolymers of vinyl compounds such as polymethyl methacrylate, polyethylene, polypropylene, polyphenylene ether, polyethylene terephthalate, polybutylene terephthalate, polycarbonate, polyamide and those reinforced with rubbery polymers And their alloys.

The flame retardant (B) means a known compound which is liquid or solid at room temperature and can impart flame retardancy by being added to a resin. Examples thereof include halogen-based and phosphorus-based flame retardants. Is mentioned. For example, examples of the halogen-based flame retardant include an aromatic halogen compound, a halogenated aromatic vinyl polymer, a halogenated cyanurate resin, a halogenated polyphenylene ether, a halogenated polyphenylene thioether, and a halogenated alkyltriazine compound. Bisphenol-based epoxy resin, brominated bisphenol-based phenoxy resin, brominated bisphenol-based polycarbonate resin, brominated polystyrene resin, brominated cross-linked polystyrene resin,
Brominated bisphenol cyanurate resin, brominated polyphenylene oxide, polydibromophenylene oxide, decabromodiphenyl oxide bisphenol condensate (tetrabromobisphenol A, oligomers thereof, etc.), and brominated alkyltriazine compounds. Examples of the phosphorus-based flame retardant include non-halogen phosphates such as trimethyl phosphate, triethyl phosphate, tributyl phosphate, trioctyl phosphate, tributoxymethyl phosphate, triphenyl phosphate, tricresyl phosphate, tricresyl diphosphate, and octyl diphenyl phosphate. Ester, tris (chloroethyl) phosphate, bis (2,
Halogen-containing esters such as (3-dibromopropyl) 2,3-dichloropropylphosphate, tris (dichloropropyl) phosphate and bis (chloropropyl) monooctylphosphate. Among them, preferred as the binder are tetrabromobisphenol A and oligomers thereof. These are one or two
More than one species can be used in combination.

[0011] The flame retardant auxiliary (C) means a known compound which can impart more excellent flame retardancy when used in combination with the flame retardant. For example, as the inorganic flame retardant, antimony trioxide, antimony tetroxide, antimony oxide such as antimony pentoxide, molybdenum oxide, molybdenum compounds such as ammonium molybdate, tin oxide, tin compounds such as tin hydroxide, Zirconium oxide, zirconium-based compounds such as zirconium hydroxide, zinc borate,
Examples thereof include boron compounds such as barium metaborate, iron oxide, and zinc sulfide. Of these, preferred
Antimony trioxide, antimony pentoxide, and molybdenum oxide. Examples of the organic flame retardant include phenol novolak resins such as phenol aldehyde novolak resins and cresol novolak resins, polytetrafluoroethylene, and silicone resins. Of these, polytetrafluoroethylene is preferred as the binder, and more preferably powdered polytetrafluoroethylene. These can be used alone or in combination of two or more.

As the heat stabilizer (D), zeolite,
Examples include hydrotalcite, metal borate, metal salt of ethylenediaminetetraacetic acid, and organic tin compounds. The zeolite referred to herein is a zeolite containing at least one metal selected from metals of Groups I, II and IV of the periodic table, and specifically has the general formula (1) Na ₂ O _{· Al 2 O 3 · SiO 2} · XH 2 O (1) ( wherein, X is a number of 0-6.) or a type zeolite represented by to replace the Na a-type zeolite with other metals Examples include Mg-substituted zeolite, Ca-substituted zeolite, Zn-substituted zeolite, and Sr-substituted zeolite.

Examples of the organotin-based compounds include dibutyltin laurate, di-n-octyltin dilaurate, dibutyltin dimaleate and copolymers thereof, dibutyltin bis (butylmaleate), dibutyltinbis (octylmaleate), di-n Octyltin bis (butyl maleate), dibutyltin laurate maleate, dimethyltin bis (octylthioglycolate), dibutyltinbis (octylthioglycolate), di-n-octyltinbis (isooctylthioglycolate), Di-n-
Octyltin-S, S'-bis (isooctylmercaptoacetate) and the like. Among these, dibutyltin dilaurate, di-n-octyltin dilaurate, dibutyltin laurate maleate, di-n-octyltin bis (isooctylthioglycolate), di-n-octyltin-S,
S'-bis (isooctyl mercaptoacetate). These can be used alone or in combination of two or more.

The method of mixing two or more components selected from the flame retardant (B), the flame retardant auxiliary (C) and the heat stabilizer (D) and forming the mixture into granules is not particularly limited. The method described in JP-A-62-298438 can be used. The term “granular” as used herein refers to a sphere, a column, or a shape similar thereto. In the present invention, at least one of the components (B) to (D) is selected from binders. The binder in the present invention refers to a component having a role of an excipient that keeps the mixture in a granular form even after being granulated by mixing with a powder. The proportion of the binder component in the granular flame retardant composition is 0.02 to 90% by weight, preferably 0.02 to 90% by weight.
It is preferably from 70 to 70% by weight, more preferably from 0.03 to 50% by weight.

The addition amount of the particulate flame retardant composition (E) is 2 to 45 parts by weight, preferably 5 to 40 parts by weight, based on 100 parts by weight of the thermoplastic resin (A). If the amount is less than 2 parts by weight, the flame retardancy of the obtained flame-retardant thermoplastic resin composition is insufficient, and if it exceeds 45 parts by weight, the impact resistance becomes poor. When mixing these and performing injection molding, if necessary, a flame retardant, a flame retardant auxiliary, a pigment, a dye, a lubricant, an antioxidant, an ultraviolet absorber, an antistatic agent, a reinforcing agent,
Various additives such as a filler and an antibacterial agent can be blended to such an extent that their physical properties are not impaired. The thermoplastic resin and the particulate flame retardant composition, and if necessary, other additives are blended,
After mixing with a tumbler or the like, it is preferable to perform melt kneading. By this operation, a molded article of the flame-retardant thermoplastic resin composition having more excellent uniformity can be obtained.

There is no particular limitation on the molding machine used for injection molding, but there are mixing nozzles, dalmage type, pin type, pineapple mixing type, cavity transfer type, throttled screw type,
It is preferable to use a molding machine provided with a screw having a mixing unit such as a static mixer type, a varistoring type, or a union carbide mixing type.

[0017]

BEST MODE FOR CARRYING OUT THE INVENTION

[0018]

EXAMPLES The present invention will be described more specifically with reference to the following examples, but the scope of the present invention is not limited to these examples.

Reference Example 1 Production of Granular Flame Retardant Composition (E-1) 3 parts by weight of antimony trioxide (average particle size: 0.79 μm), 19 parts by weight of powdered tetrabromobisphenol A, butyltin maleate-based heat stabilizer ( d ²⁵ = 1.26~1.
29, n ²⁵ = 1.50 to 1.52) 0.5 part by weight and 0.05 part by weight of powdered polytetrafluoroethylene are put into a Henschel mixer, and mixed and stirred at high speed for about 3 minutes under non-heating conditions. Granulation under non-heating conditions with a powder roll type extrusion granulator (disc die: die hole diameter 2.5 mm),
A cylindrical pellet having a diameter of 2.5 mm and a length of 2.5 to 3.5 mm was obtained.

30 g of the pellet is Φ60 mm, length 6
Place in a 0 mm cylindrical container and shake horizontally with a shaker.
Shaking was performed for 2 minutes under the conditions of a shaking width of 40 mm and a shaking number of 240 times / min. Thereafter, the pellets were passed through a 22-mesh sieve, and the shape retention was calculated from the following equation. As a result, the powdering resistance was 96.3%.

Powdering resistance (%) = W ₁ / W ₀ × 100 W ₁ : Weight of pellets remaining on sieve W ₀ : Weight of pellets before shaking Reference Example 2 Granular flame retardant composition (E-2) producing antimony trioxide (average particle diameter of): 0.79 .mu.m) 3 parts by weight, the powder tetrabromobisphenol A19 parts, butyltin maleate-based heat stabilizer (d ²⁵ 25 = 1.26 to
1.29, n ²⁵ = 1.50 to 1.52) 0.5 part by weight,
A granular flame retardant was produced in the same manner as in Reference Example 1 except that 0.05 parts by weight of powdered polytetrafluoroethylene and 10 parts by weight of powdered calcium stearate were added. The powdering resistance was 89.8%.

Example 1 45 parts by weight of an ABS resin, 55 parts by weight of an AS resin shown below,
After mixing 22.5 parts by weight of the particulate flame retardant composition (E-1) with a tumbler, the mixture was placed in a hopper of an injection molding machine equipped with a screw having a union carbide mixing unit, and injection molding was performed. A test piece for measuring physical properties was prepared at a cylinder temperature of 240 ° C and a mold temperature of 45 ° C, and a test piece for measuring flammability was prepared at a cylinder temperature of 220 ° C and a mold temperature of 60 ° C. , Intermediate products and final products. The physical properties and flammability were evaluated by the following methods. Table 1 shows the results.

ABS resin: BD rubber content = 29.8% by weight AN content in resin components excluding BD rubber = 25.4% by weight 〃 Average molecular weight Mw = 11.1 × 10 ⁴ Shape = diameter 2 mm, length 3 mm cylindrical AS resin: AN content = 25.2% by weight Average molecular weight Mw = 13.5 × 10 ⁴ Shape = 1.5 mm diameter, 3 mm long cylinder Molecular weight was measured by GPC, and polystyrene was measured. It was determined by the standard curve method as a standard sample. The measurement conditions are as follows.

Measuring equipment: Tosoh Corporation Column: Tosoh Corporation G3000HXL, G40
00HXL, G5000HXL, and G6000HXL
Developed solvent: tetrahydrofuran Flow rate: 1 ml / min BD and AN content were determined by a calibration curve method using FT-IR.

Measurement equipment: FT / IR manufactured by JASCO
7000 measurement sample: thickness 30μ by compression molding
(1) Impact Resistance (IZOD Impact Strength) Measured according to the method of ASTM D-256.

(Notched, specimen thickness 1/4 inch) (2) Flexural modulus Measured according to the method of ASTM D-790.

(3) Flammability UL94, specimen thickness 1/8, 1/12 inch, V-0
Determine the rank.

Example 2 In Example 1, the ABS resin had a thickness of 1 mm and a diameter of 2 mm.
A sample was prepared and evaluated in the same manner as in Example 1, except that a 5 mm circular plate was used.

Comparative Example 1 45 parts by weight of ABS resin pellets used in Example 1, AS
55 parts by weight of resin pellets, 3 parts by weight of antimony trioxide (average particle size: 0.79 μm), 19 parts by weight of powdered tetrabromobisphenol A, butyltin maleate-based heat stabilizer (d ²⁵ = 1.26 to 1.29, n ²⁵ = 1.50-1.
52) 1.5 parts by weight and 0.05 parts by weight of powdered polytetrafluoroethylene were mixed with a PCM30 extruder manufactured by Ikegai Co., Ltd. (biaxial co-extruder, φ = 30 mm, L / D = 33)
Then, the mixture was melt-kneaded at a temperature below the hopper of 150 ° C. and a die temperature of 240 ° C. to granulate. Under the same conditions as in Example 1, the pellets obtained at this time were subjected to physical properties measurement and flammability test specimens using an injection molding machine.

Comparative Example 2 45 parts by weight of ABS resin and 5 parts of AS resin used in Example 1
A sample was prepared in the same manner as in Example 1 except that 5 parts by weight and 32.5 parts by weight of the particulate flame retardant composition (E-2) were used.
evaluated. The results are shown in Tables 1 and 2.

[0031]

[Table 1]

[0032]

[Table 2]

[0033]

As is apparent from the above description, according to the production method of the present invention, the flame retardant is uniformly dispersed in the resin, and the flame retardant thermoplastic resin has no variation in physical properties and flame retardancy. A molded article of the composition can be provided.

──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. ⁶ Identification code Agency reference number FI Technical display location C08L 27/18 LGB C08L 27/18 LGB 55/02 LME 55/02 LME

Claims (2)

[Claims] 1. A composition comprising two or more components selected from a flame retardant (B), a flame retardant auxiliary (C) and a heat stabilizer (D) with respect to 100 parts by weight of a thermoplastic resin (A). At least one of the components (B), (C), and (D) is selected from binders, and the particulate flame retardant composition (E) contains substantially no other components. After mixing 2 to 45 parts by weight, these are melt-kneaded in an injection molding machine,
A method for producing a molded article of a flame-retardant thermoplastic resin composition, comprising injecting a melt into a mold and cooling. 2. The particulate flame retardant composition (E), wherein tetrabromobisphenol A, an oligomer thereof, polytetrafluoroethylene, dibutyltin dilaurate,
n-octyltin dilaurate, dibutyltin laurate maleate, di-n-octyltin bis (isooctylthioglycolate), and di-n-octyltin-
S, S'-bis (isooctylmercaptoacetate)
The method for producing a molded article of a flame-retardant thermoplastic resin composition according to claim 1, wherein one or two or more kinds selected from the group consisting of a binder are used as a binder.