CA1339168C - Polystyrene-based resin composition - Google Patents
Polystyrene-based resin compositionInfo
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- CA1339168C CA1339168C CA000547316A CA547316A CA1339168C CA 1339168 C CA1339168 C CA 1339168C CA 000547316 A CA000547316 A CA 000547316A CA 547316 A CA547316 A CA 547316A CA 1339168 C CA1339168 C CA 1339168C
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/524—Esters of phosphorous acids, e.g. of H3PO3
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L25/00—Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
- C08L25/02—Homopolymers or copolymers of hydrocarbons
- C08L25/04—Homopolymers or copolymers of styrene
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L25/00—Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
- C08L25/02—Homopolymers or copolymers of hydrocarbons
- C08L25/04—Homopolymers or copolymers of styrene
- C08L25/06—Polystyrene
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L53/00—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L53/02—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers of vinyl-aromatic monomers and conjugated dienes
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
- C08L2666/04—Macromolecular compounds according to groups C08L7/00 - C08L49/00, or C08L55/00 - C08L57/00; Derivatives thereof
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
- C08L2666/24—Graft or block copolymers according to groups C08L51/00, C08L53/00 or C08L55/02; Derivatives thereof
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- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
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- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
The polystyrene-based resin composition is compounded with a styrene-based polymer of which the molecular structure relative to the stereospecificity is mainly syndiotactic as determined by the NMR method and thermoplastic resins and/or an inorganic filler. The resin composition of the invention is capable of giving a molded article having well-balanced mechanical properties and thermal properties.
Description
1 339 ~ 68 A POLYSTYRENE-BASED RESIN COMPOSITION
As is well known, polymers of styrene widely under practical use are usually obtained by the free-radical poly-merization and they have an atactic structure in respect of the stereospecificity of the molecular structure. These styrene-based resins, however, are not quite satisfactory in their relatively poor heat resistance and mechanical strengths.
The inventors have continued extensive investigations to obtain a styrene-based resin freed from the disadvantages of conven-tional styrene-based resins and arrived at a discovery that the requirement can well be satisfied by using a styrene-based resin of which the molecular structure relative to the stereospecificity is-mainly syndiotactic. While such a styrene-based polymer having a mainly syndiotactic molecular structure relative to the stereospecificity, which is referred to as a syndiotactic polystyrene hereinbelow, has as such excellent heat resistance in comparison with conventional polystyrenes having an atactic molecular structure, various other properties of the resin should desirably be improved in order that the resin is very useful in a wide variety of applications.
SU~MARY OF THE IN~IENTION
The present invention accordingly has an object to provide 1 a resin composition based on a syndiotactic polystyrene and having greatly improved properties to be freed from the disad-vantages of conventional styrene-based resin compositions.
The polystyrene-based resin composition of the present inventlon compr1ses:
(a) a styrene-based polymer of which the molecular structure relative to the stereospecificity is mainly syndiotactic; and (b) an additive selected from the group consisting of thermo-plastic resins excluding of the styrene-based polymer of which the molecular structure relative to the stereospecificity is mainly syndiotactic (referred to as "thermoplastic resins"
hereinunder) and inorganic fillers.
Namely, the present invention proposes, on one hand, to compound a syndiotactic polystyrene with a thermoplastic resin lS such as polycarbonate resins so that the resultant polystyrene-based resin composition is imparted with greatly improved heat resistance, mechanical strengths and other properties in good balance as a useful molding resin composition. The invention proposes, on the other hand, to compound a syndiotactic poly-styrene with an inorganic filler such as glass fibers, optionally,in combination with a thermoplastic resin so that the resultant resin composition is imparted with further improved heat re-sistance and mechanical strengths to satisfy the requirements for molding resin compositions.
Accordingly, the invention in one aspect provides a polystyrene-based resin composition which comprises: (a) a styrene-based polymer of which the molecular structure relative to the stereospecificity is mainly syndiotactic, Bl 1 33q 1 6P~
1 selected from the group consisting of homopolymeric polystyrenes, poly (alkyl styrenes), poly (halogenated styrenes), poly (alkoxy styrenes), poly (styrene carboxylates), mixtures thereof and copolymers mainly composed thereof; and (b) an additive selected from the group consisting of a thermoplastic resin other than said styrene-based polymer having said syndiotactic molecular structure, and selected from styrene-based polymers and copolymers, polystyrenes having an atactic molecular structure, polystyrenes having an isotactic molecular structure, acrylonitrile-styrene resins, acrylonitrile-butadiene-styrene resins, styrene-butadiene-styrene block copolymers, rubbers obtained by partially or completely hydrogenating the butadiene portion of a styrene-butadiene block copolymers, condensation-polymerized polymers, polyesters, polycarbonates, polyethers, polyamides, polyoxymethylenes, acrylic polymers, poly (acrylic acid), poly (acrylic acid esters), poly (methyl methacrylate), polyolefins, polyethylene, polypropylene, polybutene, poly (4-methylpentene-1), copolymers of ethylene and propylene, polymers of vinyl halides, poly (vinyl chloride), poly (vinylidene chloride), poly (vinylidene fluoride); and an inorganic filler.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
The syndiotactic polystyrene implied in the present ~' 1 invention is a polymer of styrene of which the molecular structure relative to the stereospecificity is mainly syn-diotactic or, in other words, a polymer of styrene in which the phenyl or substituted phenyl groups as the pendant groups to the main chain of the polymeric structure are positioned alternately to the reverse directions relative to the carbon-to-carbon linkages in the polymeric main chain. The tacticity thereof can be quantitatively determined by the nuclear magnetic resonance absorption spectrometric method, referred to as the NMR method hereinbelow.
The tacticity determined by the NMR method can be expressed by the proportion of a plural number of the structural units existing in consecutive sequence such as diads, triads and pentads for two, three and five structural units, respectively.
The tacticity of the syndiotactic polystyrene as the component (a) of the inventive resin composition should be at least 85%
and at least 50% for the diads and pentads, respectively. The polystyrene having such a stereospecificity is not limited to homopolymeric polystyrenes but includes poly(alkyl styrenes), poly(halogenated styrenes), poly(alkoxy styrenes), poly(styrene carboxylates) and mixtures thereof as well as copolymers mainly composed thereof. Exemplary of the poly(alkyl styrenes), poly-(halogenated styrenes) and poly(alkoxy styrenes) are: poly-(methyl styrene), poly(ethyl styrene), poly(isopropyl styrene), poly(tert-butyl styrene) and the like; poly(chlorostyrene), poly(bromostyrene) and the like; and poly(methoxy styrene), poly(ethoxy styrene) and the like, respectively.
B~
1 The syndiotactic polystyrene of the present invention has a weight-average molecular weight of at least 100,000, prefer-ably at least 200,000. When said molecular weight is smaller than 100,000, the resin composition with sufficient heat resistance and mechanical strength can not be obtained.
When the polystyrene-based resin composition of the invention is composed of the syndiotactic polystyrene and a thermoplastic resin, the amount of the syndiotactic polystyrene in the resin composition should be in the range from 1 to 99 by weight, preferably from 5 to 95~ by weight. When the amount thereof is smaller than 1% by weight, the desired effect cannot be fully exhibited in the improvement of the heat resistance of the thermoplastic resin while an amount thereof - larger than 99% by weight results in the loss of the object of the present invention to improve the heat resistance of thermoplastic resins in general.
The basic ingredient of the inventive resin composition is an ordinary thermoplastic resin other than the above mentioned styrene-based polymers having a syndiotactic molecular structure.
The thermoplastic resin is not limited to a specific one but can be selected from a variety of thermoplastic resins depend-ing on the intended application of the resin composition.
Exemplary of the thermoplastic resin are styrene-based polymers and copolymers including polystyrenes having an atactic molecular structure, polystyrenes having an isotactic molecular structure, Acrylonitrile-styrene resins, Acrylonitrile-butadiene-styrene resins, Styrene-butadiene-styrene block copolymers, Rubbers obtained by partially or completely hydrogenating the butadiene portion of a styrene-butadiene block copolymers an~ the like, condensation-polymerized polymers including polyesters, D~
1 polycarbonates, polyethers, polyamides, polyoxymethylenes and the like, acrylic polymers including poly(acrylic acid), poly(acrylic acid esters), poly(methyl methacrylate) and the like, polyolefins including polyethylene, polypropylene, polybutene, poly(4-methylpentene-1), copolymers of ethylene and propylene and the like, polymers of vinyl halides including poly(vinyl chloride), poly(vinylidene chloride), poly(vinylidene fluoride) and the like, and so on.
The alternative additive ingredient in the inventive resin composition is an inorganic filler which is not limited to a specific one but can be selected from a variety of known inorganic fillers depending on the intended application of the resin compositiOn. Exemplary of suitable inorganic fillers are glass fibers, carbon fibers, alumina fibers, carbon black, graphite, titanium dioxide, silica, talc, mica, asbestos, calcium carbonate, calcium sulfate, barium carbonate, magnesium carbonate, tin oxide, alumina, kaolin, silicon carbide, metal powders and the like. These inorganic fillers can be used either singly or as a combination of two kinds or more accord-ing to need.
When the inventive resin composition is composed of the syndiotactic polystyrene and the inorganic filler, the weight ratio of the syndiotactic polystyrene to the inorganic filler should be in the range from 15:85 to 99:1 or, preferably, from 50:50 to 95:5.
Further, when the inventive resin composition comprises the syndiotactic polystyrene, the thermoplastic resin and the 1 inorganic filler, the formulation of the composition should contain from 5 to 50 parts by weight of the inorganic filler per 95 to 50 parts by weight of the total amount of the syn-~diotactic polystyrene and the thermoplastic resin.
S The compounding work of the above described components to prepare the inventive resin composition can be performed by using a conventional blending machine such as a Bànbury mixer, Henschel mixer, roller mill and the like. It is of course optional that the resin composition is prepared by the solution blending method.
The blending work of the components shoul~ be performed at an elevated temperature so that heat stabilizers convention-ally used in the compounding works of atactic polystyrenes cannot be used due to the dissipation and thermal decomposition.
Instead, the object of heat-stabilization of the inventive resin composition can be achieved by admixing the resin composition with from 0.005 to 5 parts by weight or, preferably, from 0.01 to 1 part by weight, per 100 parts by weight of the resinous ingredients, of a combination of a phenolic anti-oxidant and a phosphorus compound represented by the general formula ~O-CH2 ~CEI2 ~ \ p O R2 \ O--CH2 / CH2-~
in which Rl and R2 are each, independently from the other, a monovalent hydrocarbon group selected from the class consisting _ 7 _ 1 3 3 9 1 68 1 of alkyl groups having 1 to 20 carbon atoms, cycloalkyl groups having 3 to 30 carbon atoms and aryl groups having 6 to 20 carbon atoms. The weight ratio of the phosphorus compound to the phenolic antioxidant should usually be in the range from 100:1 to 1:1 or, preferably, from 10:1 to 2:1 Exemplary of the above mentioned phosphorus compound are distearyl pentaerithritol diphosphite, dioctyl pentaerithritol diphosphite, diphenyl pentaerithritol diphosphite, bis(2,4-di-tert-butyl phenyl) pentaerithritol diphosphite, bis(2,6-di-tert-butyl-4-methyl phenyl) pentaerithritol diphosphite, dicyclohexyl pentaerithritol diphosphite and the like.
The phenolic antioxidant can be any of knwon ones exemplified by 2,6-di-tert-butyl-4-methyl phenol, 2,6-diphenyl-4-methoxy phenol, 2,2'-methylene bis(6-tert-butyl-4-methyl phenol), 2,2'-methylene bis(6-tert-butyl-4-ethyl phenol), 2,2'-methylene bis[4-methyl-6-(~-methyl cyclohexyl) phenol], l,l-bis(5-tert-butyl-4-hydroxy-2-methyl phenyl) butane, 2,2'-methylene bis(4-methyl-6-cyclohexyl phenol), 2,2'-methylene bis(4-methyl-6-nonyl phenol), 1,1,3-tris(5-tert-butyl-4-hydroxy-2-methyl phenyl) butane, 2,2-bis(5-tert-butyl-4-hydroxy-2-methyl phenyl 4-n-dodecyl mercapto butane, ethylene glycol bis[3,3-bis(3-tert-butyl-4-hydroxy phenyl) butyrate], l,l-bis(3,5-dimethyl-2-hydroxy phenyl)-3-(n-dodecylthio) butane, 4,4'-thio-bis(6-tert-butyl-3-methyl phenol), 1,3,5-tris(3,5-di-tert-butyl-4-hydroxy benzyl)-2,4,6-trimethyl benzene, 2,2-bis(3,5-di-tert-butyl-4-hydroxy benzyl) malonic acid octadecyl ester, n-octadecyl 3-(4-hydroxy-3,5-di-1 tert-butyl phenyl) propionate, tetrakis[methylene(3,5-di-tert-butyl-4-hydroxy hydrocinnamate)]methane and the like.
When the inventive resin composition is prepared by com-~pounding an inorganic filler having electroconductivity, such as carbon black, graphite and the like, in an amount of 10 to60% by weight based on the overall amount of the resin composi-tion with thorough mixing, the resultant resin composition can be a heat-sensitive resistive composition having a positive temperature coefficient. It is preferable that the electro-conductive inorganic filler such as carbon black used in theabove mentioned object has a particle diameter in the range from 10 to 200 nm.
The thus obtained resin composition has greatly improved properties in the heat resistance and mechanical strengths as compared to the polystyrene-based resin compositions convention-ally used in various applications. Accordingly, the resin com-position of the invention is useful in a wide field of applica-tions as a material for various industrial uses and a material of various machines and instruments in which heat resistance and mechanical strengths higher than conventional are essential.
In the following, the polystyrene-based resin composition of the invention is described in more detail by way of examples and comparative examples.
Polymer Preparation 1. Preparation of a polystyrene resin having a mainly syndiotactic molecular structure.
Into a solution of 20 m moles of cyclopentadienyl titanium trichloride and 0.8 mole as aluminum atoms of methyl 1 aluminoxane as the catalyst constituents dissolved in 2 liters of toluene were added 3.6 liters of styrene and the polymerization of styrene was performed at 20~C for 1 hour.
After completion of the polymerization reaction, the reaction product was washed with a mixture of hydrochloric acid and methyl alcohol to decompose and remove the catalyst constituents followed by drying to give 330 g of dried polymeric product.
The polymeric product was then subjected to extraction with methyl ethyl ketone as the extraction solvent using a Soxhlet extractor. The amount of the polymer remaining as unextracted was 95% by weight of the amount before extraction.
This polymer had a weight-average molecular weight of about 280,000, number-average molecular weight of about 57,000 and melting point of 270~C. The NMR analysis of this polymer utilizing the 13C carbon isotope indicated that the NMR
absorption spectrum had a peak of absorption at 145.35 ppm which could be assigned to the syndiotactic molecular struc-ture of polystyrene. Calculation from the area of this peak gave a result that the polymer had a syndiotactivity of 96%
in pentads (refer to H. Sato & Y. Tanaka, J. Polym. Sci.
Polym. Phys. Ed. 21, 1667-1674 (1983)).
Polymer Preparation 2. Preparation of a polystyrene resin having a mainly syndiotactic molecular structure.
Into a solution of 13.4 m moles of titanium tetraethoxide and 1340 m moles as aluminum atoms of methyl aluminoxane as the catalyst constituents dissolved in 1.2 liters of toluene were added 33 liters of styrene and the polymerization - 10 - 1 3 3 q 1 6 8 1 reaction was performed for 1.5 hours at 55~C. After comple-tion of the polymerization reaction, the reaction product was washed with a mixture of hydrochloric acid and methyl ,~alcohol to decompose and remove the catalyst constituents followed by drying to give 3.5 kg of a dried polymeric product.
The polymeric product was then subjected to extraction with methyl ethyl ketone as the extraction solvent using a Soxhlet extractor. The amount of the polymer remaining unex-tracted was 95% by weight of the amount before extraction.This polymer had a weight-average molecular weight of about 800,000, number-average molecular weight of about 26,700 and melting point of 270~C. The NMP analysis of this polymer utilizing the 13C carbon isotope indicated that the NMR
absorption spectrum had a peak of absorption at 145.35 ppm which could be assigned to the syndiotactic molecular struc-ture of polystyrene. Calculation from the area of this peak gave a result that the polymer had a syndiotacticity of 97%
in pentads.
Example 1 ~ resin composition was prepared by compounding 80 parts by weight of a polycarbonate resin (Idemitsu Polycarbonate A2500, a product by Idemitsu Petrochemical Co.) as a thermo-plastic resin and 20 parts by weight of the syndiotactic polystyrene obtained in Polymer Preparation 1 described above.
The resin composition was shaped by using a Minimat molding 1 machine into test specimens of which the mechanical strengths as well as the Vicat softening point as a thermal property were measured to give the results shown in Table 1.
Example 2 The same experimental procedure as in Example 1 was undertaken except that the blending ratio of the polycarbonate resin and the syndiotactic polystyrene was 50:50 by weight instead of 80:20 by weight. The results of the experiment are also shown in Table 1.
Example 3 The same experimental procedure as in Example 1 was undertaken except that the blending ratio of the polycarbonate resin and the syndiotactic polystyrene was 20:80 by weight instead of 80:20 by weight. The results of the experiment are also shown in Table 1.
Example 4 The same experimental procedure as in Example 1 was undertaken except that the polycarbonate resin as a thermo-plastic resin was replaced with the same amount of a poly-ethylene terephthalate resin (Pyropet RY 533~ a product by Toyo Boseki Co.). The results of the experiment are also shown in Table 1.
~ Tr~e ~
1 Example 5 The same experimental procedure as in Example 4 was undertaken except that the blending ratio of the polyethylene ~terephthalate resin and the syndiotactic polystyrene was 50:50 by weight instead of 80:20 by weight. The results of the experiment are also shown in Table 1.
Example 6 The same experimental procedure as in Example 1 was undertaken except that the polycarbonate resin was replaced with the same amount of an ABS resin (JSR ABS 15, a product by Japan Synthetic Rubber Co.). The results of the experi-ment are also shown in Table 1.
Example 7 The same experimental procedure as in Example 6 was undertaken except that the blending ratio of the ABS resin and the syndiotactic polystyrene was 50:50 by weight instead of 80:20 by weight. The results of the experiment are also shown in Table 1.
Example 8 The same experimental procedure as in Example 1 was undertaken except that the polycarbonate resin was replaced with the same amount of a polysulfone resin (Udel Polysulfone P-1700, a product by Union Carbide Corp.). The results of the experiment are also shown in Table 1.
Example 9 The same experimental procedure as in Example 8 was undertaken except that the blending ratio of the polysulfone resin and the syndiotactic polystyrene was 50:50 by weight instead of 80:20 by weight. The results of the experiment are also shown in Table 1.
Comparative Examples 1 to 4 Without blending with the syndiotactic polystyrene, measurement of the properties was undertaken of each of the polycarbonate resin, polyethylene terephthalate resin, ABS
resin and polysulfone resin used in the preceding examples in Comparative Examples 1, 2, 3 and 4, respectively. The results of the measurements are also shown in Table 1.
Table 1 1 Tensile Ultimate Elastic Vicat soften-strength, elongation, modulus, ing point, kg/cm2 % kg/cm2 oC
Example 1 600 4.5 21,800 170 2 610 4.1 29,200 190 3 620 10.0 32,500 200 4 650 2.8 28,200 200<
580 2.6 29,200 200<
6 520 2.6 22,500 150 7 560 2.5 26,000 180 8 650 3.5 25,900 200<
9 490 3.0 28,300 200<
Comparative 15Example 1 590 120 15,200 150 2 710 7.6 26,900 200<
3 500 15.3 20,300 110 4 710 60 21,700 190 Example 10 A resin compound was prepared by blending, in a Henschel mixer, 80 parts by weight of the syndiotactic polystyrene ob-tained in Polymer Preparation 2 described above, 20 parts by weight of chopped glass fibers having an average fiber length of 3 mm (a producb by Asahi Fiber Glass Co.), 0.5 part by weight of bis(2,4-di-tert-butyl phenyl) pentaerithritol diphosphite and 0.2 part by weight of n-octadecyl 3-(4-hydroxy-2,5-dikutyl phenyl)propionate and the resin compound was 1 pelletized by kneading in and extruding out of an extruder machine. The pelletized resin compound was molded into test specimens of which the mechanical strengths were measured to give results including 1050 kg/cm2 of tensile strength, 1490 kg/cm2 of flexural strength and 98,000 kg/cm2 of elastic modulus of bending. The heat distortion temperature of the test specimens was 250~C.
Example 11 The same experimental procedure as in Example 10 was undertaken except that the blending ratio of the syndiotactic polystyrene and chopped glass fibers was 70:30 by weight instead of 80:20. The test specimens prepared from the resin compound had properties including 1120 kg/cm2 of tensile strength, 1600 kg/cm2 of flexural strength, 104,000 kg/cm2 of elastic modulus of bending and 250~C of heat distortion temperature.
Example 12 The same experimental procedure as in Example 10 was undertaken except that the chopped glass fibers as an inorganic filler were replaced with the same amount of chopped carbon fibers having a diameter of 9 ~m and an average fiber length of 3 mm. The test specimens prepared from the resin compound had properties including 1100 kg/cm2 of tensile strength, 1500 kg/cm2 of flexural strength, 90,000 kg/cm2 of elastic modulus of bending and 250~C of heat distortion temperature.
- 16 - 1 33~ 1 6~
1 Example 13 The same experimental procedure as in Example 12 was undertaken except that the blending ratio of the syndiotactic ~polystyrene and the chopped carbon fibers was 70:30 by weight instead of 80:20. The test specimens prepared from the resin compound had properties including 1200 kg/cm2 of tensile strength, 1600 kg/cm2 of flexural strength, 90,000 kg/cm2 of elastic modulus of bending and 250~C of heat distortion temperature.
Example 14 The same experimental procedure as in Example 10 was undertaken except that the chopped glass fibers as an inorganic filler were replaced with the same amount of pulver-rized mica having a fineness of 60 mesh or finer by the Tyler standard. The test specimens prepared from the resin compound had a heat distortion temperature of 230~C.
Example 15 The same experimental procedure as in Example 14 was undertaken except that the blending ratio of the syndiotactic polystyrene and the mica powder was 50:50 by weight. The test specimens prepared from the resin compound had a heat distortion temperature of 250~C.
Comparative Example 5 The same experimental procedure as in Example 10 was - 17 - 1 33~ 1 68 1 undertaken except that the syndiotactic polystyrene was replaced with the same amount of a commercial product of polystyrene resin having an atactic structure of the polymer in the stereospecificity and a weight-average molecular weight of about 300,000 (a product by Idemitsu Petrochemical Co.).
The test specimens prepared from the resin compound had properties including 650 kg/cm2 of tensile strength, 690 kg/cm2 of flexural strength, 36,000 kg/cm2 of elastic modulus of bending and 110~C of heat distortion temperature.
Example 16 A resin compound was prepared by blending, in a Henschel mixer, 40 parts by weight of the syndiotactic polystyrene obtained in Polymer Preparation 2 described above, 40 parts by weight of a commercial product of a polystyrene resin having an atactic molecular structure as a thermoplastic resin (Idemitsu Styrol US 315, a product by Idemitsu Petro-chemical Co.), 20 parts by weight of chopped glass fibers having an average fiber length of 3 mm (a product by Asahi Fiber Glass Co.), 0.5 part by weight of bis(2,4-di-tert-butyl phenyl) pentaerithritol diphosphite and 0.2 part byweight of tetrakis[methylene (3,5-di-tert-butyl-4-hydroxy hydrocinnamate)3 methane and the resin compound was pel-letized by kneading in and extruding out of an extruder machine. The pelletized resin compound was shaped into test specimens of which the mechanical and thermal properties were measured to give the results shown in Table 2 below.
1 33~ 1 68 1 Examples 17 to 20 The same experimental procedure as in Example 16 was undertaken in each of Examples 17 to 20 except that the ~atactic polystyrene used as a thermoplastic resin was replaced each with the same amount of the polycarbonate resin used in Example 1, the polyethylene terephthalate resin used in Example 4, the ABS resin used in Example 6 and the polysulfone resin used in Example 8, respectively. Table 2 also shows the mechanical and thermal properties of the test specimens prepared from the resin compounds.
Table 2 Tensile Ultimate Elastic Vicat soften-Example strength, elongation, modulus, ing point, No. kg/cm2 % kg/cm2 ~C
16 870 1.3 80,000 200<
17 920 2.0105,000 200<
18 950 1.4110,000 200<
19 840 1.4 94,000 200<
740 1.6102,000 200<
Example 21 A resin compound was prepared, in a Labo-plastomill, by blending 60 parts by weight of the syndiotactic polystyrene prepared in Polymer Preparation 2 described above and 40 parts by weight of carbon black having an average particle diameter of 43 nm (Diablack E, a product by ~itsubishi Chemical Industry Co.) and kneading the blend at 295~C for 1 20 minutes. The resin compound was pelletized and then compression-molded into a sheet in a compression molding machine at 300~C under a pressure of 150 kg/cm2 taking 10 minutes.
The thus prepared resin sheet was sandwiched between two foils of electrolytic nickel and pressed under the same conditions as above so that the nickel foils were bonded to and integrated with the resin sheet to give a laminated sheet having a thickness of 1 mm. Test pieces of each 1 cm by 1 cm wide were prepared by cutting the laminated sheet and sub-jected to the measurement of the electric properties utilizing the two nickel foils on both sides of the resin sheet as the electrodes.
The electrical measurement gave a result that the specific resistance of the resin sheet was 1.0 ohm cm at room temperature. The specific resistance showed a rapid increase by temperature elevation at 280~C to give a value which was larger than that at room temperature by 102 5 times. The characteristic of power consumption as a heater element was examined to find that the heat evolution cor-responded to 2.4 watts in the steady-value region where the product of the current and voltage had a constant value.
As is well known, polymers of styrene widely under practical use are usually obtained by the free-radical poly-merization and they have an atactic structure in respect of the stereospecificity of the molecular structure. These styrene-based resins, however, are not quite satisfactory in their relatively poor heat resistance and mechanical strengths.
The inventors have continued extensive investigations to obtain a styrene-based resin freed from the disadvantages of conven-tional styrene-based resins and arrived at a discovery that the requirement can well be satisfied by using a styrene-based resin of which the molecular structure relative to the stereospecificity is-mainly syndiotactic. While such a styrene-based polymer having a mainly syndiotactic molecular structure relative to the stereospecificity, which is referred to as a syndiotactic polystyrene hereinbelow, has as such excellent heat resistance in comparison with conventional polystyrenes having an atactic molecular structure, various other properties of the resin should desirably be improved in order that the resin is very useful in a wide variety of applications.
SU~MARY OF THE IN~IENTION
The present invention accordingly has an object to provide 1 a resin composition based on a syndiotactic polystyrene and having greatly improved properties to be freed from the disad-vantages of conventional styrene-based resin compositions.
The polystyrene-based resin composition of the present inventlon compr1ses:
(a) a styrene-based polymer of which the molecular structure relative to the stereospecificity is mainly syndiotactic; and (b) an additive selected from the group consisting of thermo-plastic resins excluding of the styrene-based polymer of which the molecular structure relative to the stereospecificity is mainly syndiotactic (referred to as "thermoplastic resins"
hereinunder) and inorganic fillers.
Namely, the present invention proposes, on one hand, to compound a syndiotactic polystyrene with a thermoplastic resin lS such as polycarbonate resins so that the resultant polystyrene-based resin composition is imparted with greatly improved heat resistance, mechanical strengths and other properties in good balance as a useful molding resin composition. The invention proposes, on the other hand, to compound a syndiotactic poly-styrene with an inorganic filler such as glass fibers, optionally,in combination with a thermoplastic resin so that the resultant resin composition is imparted with further improved heat re-sistance and mechanical strengths to satisfy the requirements for molding resin compositions.
Accordingly, the invention in one aspect provides a polystyrene-based resin composition which comprises: (a) a styrene-based polymer of which the molecular structure relative to the stereospecificity is mainly syndiotactic, Bl 1 33q 1 6P~
1 selected from the group consisting of homopolymeric polystyrenes, poly (alkyl styrenes), poly (halogenated styrenes), poly (alkoxy styrenes), poly (styrene carboxylates), mixtures thereof and copolymers mainly composed thereof; and (b) an additive selected from the group consisting of a thermoplastic resin other than said styrene-based polymer having said syndiotactic molecular structure, and selected from styrene-based polymers and copolymers, polystyrenes having an atactic molecular structure, polystyrenes having an isotactic molecular structure, acrylonitrile-styrene resins, acrylonitrile-butadiene-styrene resins, styrene-butadiene-styrene block copolymers, rubbers obtained by partially or completely hydrogenating the butadiene portion of a styrene-butadiene block copolymers, condensation-polymerized polymers, polyesters, polycarbonates, polyethers, polyamides, polyoxymethylenes, acrylic polymers, poly (acrylic acid), poly (acrylic acid esters), poly (methyl methacrylate), polyolefins, polyethylene, polypropylene, polybutene, poly (4-methylpentene-1), copolymers of ethylene and propylene, polymers of vinyl halides, poly (vinyl chloride), poly (vinylidene chloride), poly (vinylidene fluoride); and an inorganic filler.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
The syndiotactic polystyrene implied in the present ~' 1 invention is a polymer of styrene of which the molecular structure relative to the stereospecificity is mainly syn-diotactic or, in other words, a polymer of styrene in which the phenyl or substituted phenyl groups as the pendant groups to the main chain of the polymeric structure are positioned alternately to the reverse directions relative to the carbon-to-carbon linkages in the polymeric main chain. The tacticity thereof can be quantitatively determined by the nuclear magnetic resonance absorption spectrometric method, referred to as the NMR method hereinbelow.
The tacticity determined by the NMR method can be expressed by the proportion of a plural number of the structural units existing in consecutive sequence such as diads, triads and pentads for two, three and five structural units, respectively.
The tacticity of the syndiotactic polystyrene as the component (a) of the inventive resin composition should be at least 85%
and at least 50% for the diads and pentads, respectively. The polystyrene having such a stereospecificity is not limited to homopolymeric polystyrenes but includes poly(alkyl styrenes), poly(halogenated styrenes), poly(alkoxy styrenes), poly(styrene carboxylates) and mixtures thereof as well as copolymers mainly composed thereof. Exemplary of the poly(alkyl styrenes), poly-(halogenated styrenes) and poly(alkoxy styrenes) are: poly-(methyl styrene), poly(ethyl styrene), poly(isopropyl styrene), poly(tert-butyl styrene) and the like; poly(chlorostyrene), poly(bromostyrene) and the like; and poly(methoxy styrene), poly(ethoxy styrene) and the like, respectively.
B~
1 The syndiotactic polystyrene of the present invention has a weight-average molecular weight of at least 100,000, prefer-ably at least 200,000. When said molecular weight is smaller than 100,000, the resin composition with sufficient heat resistance and mechanical strength can not be obtained.
When the polystyrene-based resin composition of the invention is composed of the syndiotactic polystyrene and a thermoplastic resin, the amount of the syndiotactic polystyrene in the resin composition should be in the range from 1 to 99 by weight, preferably from 5 to 95~ by weight. When the amount thereof is smaller than 1% by weight, the desired effect cannot be fully exhibited in the improvement of the heat resistance of the thermoplastic resin while an amount thereof - larger than 99% by weight results in the loss of the object of the present invention to improve the heat resistance of thermoplastic resins in general.
The basic ingredient of the inventive resin composition is an ordinary thermoplastic resin other than the above mentioned styrene-based polymers having a syndiotactic molecular structure.
The thermoplastic resin is not limited to a specific one but can be selected from a variety of thermoplastic resins depend-ing on the intended application of the resin composition.
Exemplary of the thermoplastic resin are styrene-based polymers and copolymers including polystyrenes having an atactic molecular structure, polystyrenes having an isotactic molecular structure, Acrylonitrile-styrene resins, Acrylonitrile-butadiene-styrene resins, Styrene-butadiene-styrene block copolymers, Rubbers obtained by partially or completely hydrogenating the butadiene portion of a styrene-butadiene block copolymers an~ the like, condensation-polymerized polymers including polyesters, D~
1 polycarbonates, polyethers, polyamides, polyoxymethylenes and the like, acrylic polymers including poly(acrylic acid), poly(acrylic acid esters), poly(methyl methacrylate) and the like, polyolefins including polyethylene, polypropylene, polybutene, poly(4-methylpentene-1), copolymers of ethylene and propylene and the like, polymers of vinyl halides including poly(vinyl chloride), poly(vinylidene chloride), poly(vinylidene fluoride) and the like, and so on.
The alternative additive ingredient in the inventive resin composition is an inorganic filler which is not limited to a specific one but can be selected from a variety of known inorganic fillers depending on the intended application of the resin compositiOn. Exemplary of suitable inorganic fillers are glass fibers, carbon fibers, alumina fibers, carbon black, graphite, titanium dioxide, silica, talc, mica, asbestos, calcium carbonate, calcium sulfate, barium carbonate, magnesium carbonate, tin oxide, alumina, kaolin, silicon carbide, metal powders and the like. These inorganic fillers can be used either singly or as a combination of two kinds or more accord-ing to need.
When the inventive resin composition is composed of the syndiotactic polystyrene and the inorganic filler, the weight ratio of the syndiotactic polystyrene to the inorganic filler should be in the range from 15:85 to 99:1 or, preferably, from 50:50 to 95:5.
Further, when the inventive resin composition comprises the syndiotactic polystyrene, the thermoplastic resin and the 1 inorganic filler, the formulation of the composition should contain from 5 to 50 parts by weight of the inorganic filler per 95 to 50 parts by weight of the total amount of the syn-~diotactic polystyrene and the thermoplastic resin.
S The compounding work of the above described components to prepare the inventive resin composition can be performed by using a conventional blending machine such as a Bànbury mixer, Henschel mixer, roller mill and the like. It is of course optional that the resin composition is prepared by the solution blending method.
The blending work of the components shoul~ be performed at an elevated temperature so that heat stabilizers convention-ally used in the compounding works of atactic polystyrenes cannot be used due to the dissipation and thermal decomposition.
Instead, the object of heat-stabilization of the inventive resin composition can be achieved by admixing the resin composition with from 0.005 to 5 parts by weight or, preferably, from 0.01 to 1 part by weight, per 100 parts by weight of the resinous ingredients, of a combination of a phenolic anti-oxidant and a phosphorus compound represented by the general formula ~O-CH2 ~CEI2 ~ \ p O R2 \ O--CH2 / CH2-~
in which Rl and R2 are each, independently from the other, a monovalent hydrocarbon group selected from the class consisting _ 7 _ 1 3 3 9 1 68 1 of alkyl groups having 1 to 20 carbon atoms, cycloalkyl groups having 3 to 30 carbon atoms and aryl groups having 6 to 20 carbon atoms. The weight ratio of the phosphorus compound to the phenolic antioxidant should usually be in the range from 100:1 to 1:1 or, preferably, from 10:1 to 2:1 Exemplary of the above mentioned phosphorus compound are distearyl pentaerithritol diphosphite, dioctyl pentaerithritol diphosphite, diphenyl pentaerithritol diphosphite, bis(2,4-di-tert-butyl phenyl) pentaerithritol diphosphite, bis(2,6-di-tert-butyl-4-methyl phenyl) pentaerithritol diphosphite, dicyclohexyl pentaerithritol diphosphite and the like.
The phenolic antioxidant can be any of knwon ones exemplified by 2,6-di-tert-butyl-4-methyl phenol, 2,6-diphenyl-4-methoxy phenol, 2,2'-methylene bis(6-tert-butyl-4-methyl phenol), 2,2'-methylene bis(6-tert-butyl-4-ethyl phenol), 2,2'-methylene bis[4-methyl-6-(~-methyl cyclohexyl) phenol], l,l-bis(5-tert-butyl-4-hydroxy-2-methyl phenyl) butane, 2,2'-methylene bis(4-methyl-6-cyclohexyl phenol), 2,2'-methylene bis(4-methyl-6-nonyl phenol), 1,1,3-tris(5-tert-butyl-4-hydroxy-2-methyl phenyl) butane, 2,2-bis(5-tert-butyl-4-hydroxy-2-methyl phenyl 4-n-dodecyl mercapto butane, ethylene glycol bis[3,3-bis(3-tert-butyl-4-hydroxy phenyl) butyrate], l,l-bis(3,5-dimethyl-2-hydroxy phenyl)-3-(n-dodecylthio) butane, 4,4'-thio-bis(6-tert-butyl-3-methyl phenol), 1,3,5-tris(3,5-di-tert-butyl-4-hydroxy benzyl)-2,4,6-trimethyl benzene, 2,2-bis(3,5-di-tert-butyl-4-hydroxy benzyl) malonic acid octadecyl ester, n-octadecyl 3-(4-hydroxy-3,5-di-1 tert-butyl phenyl) propionate, tetrakis[methylene(3,5-di-tert-butyl-4-hydroxy hydrocinnamate)]methane and the like.
When the inventive resin composition is prepared by com-~pounding an inorganic filler having electroconductivity, such as carbon black, graphite and the like, in an amount of 10 to60% by weight based on the overall amount of the resin composi-tion with thorough mixing, the resultant resin composition can be a heat-sensitive resistive composition having a positive temperature coefficient. It is preferable that the electro-conductive inorganic filler such as carbon black used in theabove mentioned object has a particle diameter in the range from 10 to 200 nm.
The thus obtained resin composition has greatly improved properties in the heat resistance and mechanical strengths as compared to the polystyrene-based resin compositions convention-ally used in various applications. Accordingly, the resin com-position of the invention is useful in a wide field of applica-tions as a material for various industrial uses and a material of various machines and instruments in which heat resistance and mechanical strengths higher than conventional are essential.
In the following, the polystyrene-based resin composition of the invention is described in more detail by way of examples and comparative examples.
Polymer Preparation 1. Preparation of a polystyrene resin having a mainly syndiotactic molecular structure.
Into a solution of 20 m moles of cyclopentadienyl titanium trichloride and 0.8 mole as aluminum atoms of methyl 1 aluminoxane as the catalyst constituents dissolved in 2 liters of toluene were added 3.6 liters of styrene and the polymerization of styrene was performed at 20~C for 1 hour.
After completion of the polymerization reaction, the reaction product was washed with a mixture of hydrochloric acid and methyl alcohol to decompose and remove the catalyst constituents followed by drying to give 330 g of dried polymeric product.
The polymeric product was then subjected to extraction with methyl ethyl ketone as the extraction solvent using a Soxhlet extractor. The amount of the polymer remaining as unextracted was 95% by weight of the amount before extraction.
This polymer had a weight-average molecular weight of about 280,000, number-average molecular weight of about 57,000 and melting point of 270~C. The NMR analysis of this polymer utilizing the 13C carbon isotope indicated that the NMR
absorption spectrum had a peak of absorption at 145.35 ppm which could be assigned to the syndiotactic molecular struc-ture of polystyrene. Calculation from the area of this peak gave a result that the polymer had a syndiotactivity of 96%
in pentads (refer to H. Sato & Y. Tanaka, J. Polym. Sci.
Polym. Phys. Ed. 21, 1667-1674 (1983)).
Polymer Preparation 2. Preparation of a polystyrene resin having a mainly syndiotactic molecular structure.
Into a solution of 13.4 m moles of titanium tetraethoxide and 1340 m moles as aluminum atoms of methyl aluminoxane as the catalyst constituents dissolved in 1.2 liters of toluene were added 33 liters of styrene and the polymerization - 10 - 1 3 3 q 1 6 8 1 reaction was performed for 1.5 hours at 55~C. After comple-tion of the polymerization reaction, the reaction product was washed with a mixture of hydrochloric acid and methyl ,~alcohol to decompose and remove the catalyst constituents followed by drying to give 3.5 kg of a dried polymeric product.
The polymeric product was then subjected to extraction with methyl ethyl ketone as the extraction solvent using a Soxhlet extractor. The amount of the polymer remaining unex-tracted was 95% by weight of the amount before extraction.This polymer had a weight-average molecular weight of about 800,000, number-average molecular weight of about 26,700 and melting point of 270~C. The NMP analysis of this polymer utilizing the 13C carbon isotope indicated that the NMR
absorption spectrum had a peak of absorption at 145.35 ppm which could be assigned to the syndiotactic molecular struc-ture of polystyrene. Calculation from the area of this peak gave a result that the polymer had a syndiotacticity of 97%
in pentads.
Example 1 ~ resin composition was prepared by compounding 80 parts by weight of a polycarbonate resin (Idemitsu Polycarbonate A2500, a product by Idemitsu Petrochemical Co.) as a thermo-plastic resin and 20 parts by weight of the syndiotactic polystyrene obtained in Polymer Preparation 1 described above.
The resin composition was shaped by using a Minimat molding 1 machine into test specimens of which the mechanical strengths as well as the Vicat softening point as a thermal property were measured to give the results shown in Table 1.
Example 2 The same experimental procedure as in Example 1 was undertaken except that the blending ratio of the polycarbonate resin and the syndiotactic polystyrene was 50:50 by weight instead of 80:20 by weight. The results of the experiment are also shown in Table 1.
Example 3 The same experimental procedure as in Example 1 was undertaken except that the blending ratio of the polycarbonate resin and the syndiotactic polystyrene was 20:80 by weight instead of 80:20 by weight. The results of the experiment are also shown in Table 1.
Example 4 The same experimental procedure as in Example 1 was undertaken except that the polycarbonate resin as a thermo-plastic resin was replaced with the same amount of a poly-ethylene terephthalate resin (Pyropet RY 533~ a product by Toyo Boseki Co.). The results of the experiment are also shown in Table 1.
~ Tr~e ~
1 Example 5 The same experimental procedure as in Example 4 was undertaken except that the blending ratio of the polyethylene ~terephthalate resin and the syndiotactic polystyrene was 50:50 by weight instead of 80:20 by weight. The results of the experiment are also shown in Table 1.
Example 6 The same experimental procedure as in Example 1 was undertaken except that the polycarbonate resin was replaced with the same amount of an ABS resin (JSR ABS 15, a product by Japan Synthetic Rubber Co.). The results of the experi-ment are also shown in Table 1.
Example 7 The same experimental procedure as in Example 6 was undertaken except that the blending ratio of the ABS resin and the syndiotactic polystyrene was 50:50 by weight instead of 80:20 by weight. The results of the experiment are also shown in Table 1.
Example 8 The same experimental procedure as in Example 1 was undertaken except that the polycarbonate resin was replaced with the same amount of a polysulfone resin (Udel Polysulfone P-1700, a product by Union Carbide Corp.). The results of the experiment are also shown in Table 1.
Example 9 The same experimental procedure as in Example 8 was undertaken except that the blending ratio of the polysulfone resin and the syndiotactic polystyrene was 50:50 by weight instead of 80:20 by weight. The results of the experiment are also shown in Table 1.
Comparative Examples 1 to 4 Without blending with the syndiotactic polystyrene, measurement of the properties was undertaken of each of the polycarbonate resin, polyethylene terephthalate resin, ABS
resin and polysulfone resin used in the preceding examples in Comparative Examples 1, 2, 3 and 4, respectively. The results of the measurements are also shown in Table 1.
Table 1 1 Tensile Ultimate Elastic Vicat soften-strength, elongation, modulus, ing point, kg/cm2 % kg/cm2 oC
Example 1 600 4.5 21,800 170 2 610 4.1 29,200 190 3 620 10.0 32,500 200 4 650 2.8 28,200 200<
580 2.6 29,200 200<
6 520 2.6 22,500 150 7 560 2.5 26,000 180 8 650 3.5 25,900 200<
9 490 3.0 28,300 200<
Comparative 15Example 1 590 120 15,200 150 2 710 7.6 26,900 200<
3 500 15.3 20,300 110 4 710 60 21,700 190 Example 10 A resin compound was prepared by blending, in a Henschel mixer, 80 parts by weight of the syndiotactic polystyrene ob-tained in Polymer Preparation 2 described above, 20 parts by weight of chopped glass fibers having an average fiber length of 3 mm (a producb by Asahi Fiber Glass Co.), 0.5 part by weight of bis(2,4-di-tert-butyl phenyl) pentaerithritol diphosphite and 0.2 part by weight of n-octadecyl 3-(4-hydroxy-2,5-dikutyl phenyl)propionate and the resin compound was 1 pelletized by kneading in and extruding out of an extruder machine. The pelletized resin compound was molded into test specimens of which the mechanical strengths were measured to give results including 1050 kg/cm2 of tensile strength, 1490 kg/cm2 of flexural strength and 98,000 kg/cm2 of elastic modulus of bending. The heat distortion temperature of the test specimens was 250~C.
Example 11 The same experimental procedure as in Example 10 was undertaken except that the blending ratio of the syndiotactic polystyrene and chopped glass fibers was 70:30 by weight instead of 80:20. The test specimens prepared from the resin compound had properties including 1120 kg/cm2 of tensile strength, 1600 kg/cm2 of flexural strength, 104,000 kg/cm2 of elastic modulus of bending and 250~C of heat distortion temperature.
Example 12 The same experimental procedure as in Example 10 was undertaken except that the chopped glass fibers as an inorganic filler were replaced with the same amount of chopped carbon fibers having a diameter of 9 ~m and an average fiber length of 3 mm. The test specimens prepared from the resin compound had properties including 1100 kg/cm2 of tensile strength, 1500 kg/cm2 of flexural strength, 90,000 kg/cm2 of elastic modulus of bending and 250~C of heat distortion temperature.
- 16 - 1 33~ 1 6~
1 Example 13 The same experimental procedure as in Example 12 was undertaken except that the blending ratio of the syndiotactic ~polystyrene and the chopped carbon fibers was 70:30 by weight instead of 80:20. The test specimens prepared from the resin compound had properties including 1200 kg/cm2 of tensile strength, 1600 kg/cm2 of flexural strength, 90,000 kg/cm2 of elastic modulus of bending and 250~C of heat distortion temperature.
Example 14 The same experimental procedure as in Example 10 was undertaken except that the chopped glass fibers as an inorganic filler were replaced with the same amount of pulver-rized mica having a fineness of 60 mesh or finer by the Tyler standard. The test specimens prepared from the resin compound had a heat distortion temperature of 230~C.
Example 15 The same experimental procedure as in Example 14 was undertaken except that the blending ratio of the syndiotactic polystyrene and the mica powder was 50:50 by weight. The test specimens prepared from the resin compound had a heat distortion temperature of 250~C.
Comparative Example 5 The same experimental procedure as in Example 10 was - 17 - 1 33~ 1 68 1 undertaken except that the syndiotactic polystyrene was replaced with the same amount of a commercial product of polystyrene resin having an atactic structure of the polymer in the stereospecificity and a weight-average molecular weight of about 300,000 (a product by Idemitsu Petrochemical Co.).
The test specimens prepared from the resin compound had properties including 650 kg/cm2 of tensile strength, 690 kg/cm2 of flexural strength, 36,000 kg/cm2 of elastic modulus of bending and 110~C of heat distortion temperature.
Example 16 A resin compound was prepared by blending, in a Henschel mixer, 40 parts by weight of the syndiotactic polystyrene obtained in Polymer Preparation 2 described above, 40 parts by weight of a commercial product of a polystyrene resin having an atactic molecular structure as a thermoplastic resin (Idemitsu Styrol US 315, a product by Idemitsu Petro-chemical Co.), 20 parts by weight of chopped glass fibers having an average fiber length of 3 mm (a product by Asahi Fiber Glass Co.), 0.5 part by weight of bis(2,4-di-tert-butyl phenyl) pentaerithritol diphosphite and 0.2 part byweight of tetrakis[methylene (3,5-di-tert-butyl-4-hydroxy hydrocinnamate)3 methane and the resin compound was pel-letized by kneading in and extruding out of an extruder machine. The pelletized resin compound was shaped into test specimens of which the mechanical and thermal properties were measured to give the results shown in Table 2 below.
1 33~ 1 68 1 Examples 17 to 20 The same experimental procedure as in Example 16 was undertaken in each of Examples 17 to 20 except that the ~atactic polystyrene used as a thermoplastic resin was replaced each with the same amount of the polycarbonate resin used in Example 1, the polyethylene terephthalate resin used in Example 4, the ABS resin used in Example 6 and the polysulfone resin used in Example 8, respectively. Table 2 also shows the mechanical and thermal properties of the test specimens prepared from the resin compounds.
Table 2 Tensile Ultimate Elastic Vicat soften-Example strength, elongation, modulus, ing point, No. kg/cm2 % kg/cm2 ~C
16 870 1.3 80,000 200<
17 920 2.0105,000 200<
18 950 1.4110,000 200<
19 840 1.4 94,000 200<
740 1.6102,000 200<
Example 21 A resin compound was prepared, in a Labo-plastomill, by blending 60 parts by weight of the syndiotactic polystyrene prepared in Polymer Preparation 2 described above and 40 parts by weight of carbon black having an average particle diameter of 43 nm (Diablack E, a product by ~itsubishi Chemical Industry Co.) and kneading the blend at 295~C for 1 20 minutes. The resin compound was pelletized and then compression-molded into a sheet in a compression molding machine at 300~C under a pressure of 150 kg/cm2 taking 10 minutes.
The thus prepared resin sheet was sandwiched between two foils of electrolytic nickel and pressed under the same conditions as above so that the nickel foils were bonded to and integrated with the resin sheet to give a laminated sheet having a thickness of 1 mm. Test pieces of each 1 cm by 1 cm wide were prepared by cutting the laminated sheet and sub-jected to the measurement of the electric properties utilizing the two nickel foils on both sides of the resin sheet as the electrodes.
The electrical measurement gave a result that the specific resistance of the resin sheet was 1.0 ohm cm at room temperature. The specific resistance showed a rapid increase by temperature elevation at 280~C to give a value which was larger than that at room temperature by 102 5 times. The characteristic of power consumption as a heater element was examined to find that the heat evolution cor-responded to 2.4 watts in the steady-value region where the product of the current and voltage had a constant value.
Claims (10)
1. A polystyrene-based resin composition which comprises:
(a) a styrene-based polymer of which the molecular structure relative to the stereospecificity is mainly syndiotactic, selected from the group consisting of homopolymeric polystyrenes, poly (alkyl styrenes), poly (halogenated styrenes), poly (alkoxy styrenes), poly (styrene carboxylates), mixtures thereof and copolymers mainly composed thereof; and (b) an additive selected from the group consisting of a thermoplastic resin other than said styrene-based polymer having said syndiotactic molecular structure, and selected from styrene-based polymers and copolymers, polystyrenes having an atactic molecular structure, polystyrenes having an isotactic molecular structure, acrylonitrile-styrene resins, acrylonitrile-butadiene-styrene resins, styrene-butadiene-styrene block copolymers, rubbers obtained by partially or completely hydrogenating the butadiene portion of a styrene-butadiene block copolymers, condensation-polymerized polymers, polyesters, polycarbonates, polyethers, polyamides, polyoxymethylenes, acrylic polymers, poly (acrylic acid), poly (acrylic acid esters), poly (methyl methacrylate), polyolefins, polyethylene, polypropylene, polybutene, poly (4-methylpentene-l), copolymers of ethylene and propylene, polymers of vinyl halides, poly (vinyl chloride), poly (vinylidene chloride), poly (vinylidene fluoride); and an inorganic filler.
(a) a styrene-based polymer of which the molecular structure relative to the stereospecificity is mainly syndiotactic, selected from the group consisting of homopolymeric polystyrenes, poly (alkyl styrenes), poly (halogenated styrenes), poly (alkoxy styrenes), poly (styrene carboxylates), mixtures thereof and copolymers mainly composed thereof; and (b) an additive selected from the group consisting of a thermoplastic resin other than said styrene-based polymer having said syndiotactic molecular structure, and selected from styrene-based polymers and copolymers, polystyrenes having an atactic molecular structure, polystyrenes having an isotactic molecular structure, acrylonitrile-styrene resins, acrylonitrile-butadiene-styrene resins, styrene-butadiene-styrene block copolymers, rubbers obtained by partially or completely hydrogenating the butadiene portion of a styrene-butadiene block copolymers, condensation-polymerized polymers, polyesters, polycarbonates, polyethers, polyamides, polyoxymethylenes, acrylic polymers, poly (acrylic acid), poly (acrylic acid esters), poly (methyl methacrylate), polyolefins, polyethylene, polypropylene, polybutene, poly (4-methylpentene-l), copolymers of ethylene and propylene, polymers of vinyl halides, poly (vinyl chloride), poly (vinylidene chloride), poly (vinylidene fluoride); and an inorganic filler.
2. The polystyrene-based resin composition as claimed in claim 1 wherein the styrene-based polymer as the component (a) has a tacticity of at least 85% in diads or at least 50%
in pentads as measured by the method of nuclear magnetic absorption spectroscopy.
in pentads as measured by the method of nuclear magnetic absorption spectroscopy.
3. The polystyrene-based resin composition as claimed in claim 1 wherein the styrene-based polymer as the component (a) has a weight-average molecular weight of at least 100,000.
4. The polystyrene-based resin composition as claimed in claim 1 wherein the styrene-based polymer as the component (a) is a polymer of a monomer selected from the group consisting of styrene, alkyl styrenes, halogenated styrenes and alkoxy styrenes.
5. The polystyrene-based resin composition as claimed in claim 1 wherein the amount of the thermoplastic resin as the component (b) is in the range from 99 to 1 part by weight per 1 to 99 parts by weight of the styrene-based polymer as the component (a).
6. The polystyrene-based resin composition as claimed in claim 5 wherein the amount of the thermoplastic resin as the component (b) is in the range from 95 to 5 parts by weight per 5 to 95 parts by weight of the styrene-based polymer as the component (a).
7. The polystyrene-based resin composition as claimed in claim 1 wherein the amount of the inorganic filler as the component (b) is in the range from 85 to 1 part by weight per 15 to 99 parts by weight of the styrene-based polymer as the component (a).
8. The polystyrene-based resin composition as claimed in claim 7 wherein the amount of the inorganic filler as the component (b) is in the range from 50 to 5 parts by weight per 50 to 95 parts by weight of the styrene-based polymer as the component (a).
9. The polystyrene-based resin composition as claimed in claim 1 wherein the styrene-based polymer as the component (a) is compounded with the thermoplastic resin as the component (b) and the inorganic filler as the component (b) in such a ratio that the amount of the inorganic filler as the component (b) is in the range from 50 to 5 parts by weight per 50 to 95 parts by weight of the total amount of the styrene-based polymer as the component (a) and the thermoplastic resin as the component (b).
10. The polystyrene-based resin composition as claimed in claim 1 which further comprises:
(c) a pentaerithritol diphosphite represented by the general formula , in which R1 and R2 are each, independently from the other, a monovalent hydrocarbon group selected from the group consisting of alkyl groups having 1 to 20 carbon atoms, cycloalkyl groups having 3 to 20 carbon atoms and aryl groups having 6 to 20 carbon atoms; and (d) a phenolic antioxidant.
(c) a pentaerithritol diphosphite represented by the general formula , in which R1 and R2 are each, independently from the other, a monovalent hydrocarbon group selected from the group consisting of alkyl groups having 1 to 20 carbon atoms, cycloalkyl groups having 3 to 20 carbon atoms and aryl groups having 6 to 20 carbon atoms; and (d) a phenolic antioxidant.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA000547316A CA1339168C (en) | 1987-09-18 | 1987-09-18 | Polystyrene-based resin composition |
| US09/075,867 US5990217A (en) | 1986-05-06 | 1998-05-12 | Styrene based resin composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA000547316A CA1339168C (en) | 1987-09-18 | 1987-09-18 | Polystyrene-based resin composition |
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| Publication Number | Publication Date |
|---|---|
| CA1339168C true CA1339168C (en) | 1997-07-29 |
Family
ID=4136484
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000547316A Expired - Fee Related CA1339168C (en) | 1986-05-06 | 1987-09-18 | Polystyrene-based resin composition |
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| Country | Link |
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| CA (1) | CA1339168C (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN117563685A (en) * | 2024-01-16 | 2024-02-20 | 山东晶源环保科技有限公司 | Efficient wastewater defluorinating agent and preparation and use methods thereof |
-
1987
- 1987-09-18 CA CA000547316A patent/CA1339168C/en not_active Expired - Fee Related
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN117563685A (en) * | 2024-01-16 | 2024-02-20 | 山东晶源环保科技有限公司 | Efficient wastewater defluorinating agent and preparation and use methods thereof |
| CN117563685B (en) * | 2024-01-16 | 2024-04-02 | 山东晶源环保科技有限公司 | Efficient wastewater defluorinating agent and preparation and use methods thereof |
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