WO1995029956A1 - Composition de resine thermoplastique - Google Patents
Composition de resine thermoplastique Download PDFInfo
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- WO1995029956A1 WO1995029956A1 PCT/JP1995/000833 JP9500833W WO9529956A1 WO 1995029956 A1 WO1995029956 A1 WO 1995029956A1 JP 9500833 W JP9500833 W JP 9500833W WO 9529956 A1 WO9529956 A1 WO 9529956A1
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- methylol group
- resin composition
- thermoplastic resin
- polymer
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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
- C08L27/00—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 a halogen; Compositions of derivatives of such polymers
- C08L27/02—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 a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/12—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 a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
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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
- C08L27/00—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 a halogen; Compositions of derivatives of such polymers
- C08L27/02—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 a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/12—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 a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
- C08L27/18—Homopolymers or copolymers or tetrafluoroethene
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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
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
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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
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
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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
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/04—Polyesters derived from hydroxycarboxylic acids, e.g. lactones
Definitions
- the present invention is intended to improve the mutual dispersibility and interfacial adhesiveness of a premix obtained by mixing a perfluoro polymer and a liquid crystal polyester.
- the present invention relates to an improved thermoplastic resin composition. For further details, see the molecular chain terminal tree of perfluoropolymer.
- the present invention relates to a thermoplastic resin composition
- a thermoplastic resin composition comprising a blend obtained by mixing a thermoplastic resin with a thermoplastic resin.
- Fluorocarbon fluororesins for example, PTFE, FEP, PFA, etc.
- PTFE fluorocarbon fluororesins
- FEP fluorocarbon fluororesins
- PFA poly(ethylene glycol)
- Fluorocarbon fluororesins have a wide usable temperature range and are resistant to chemicals, alkali, acid, and water. It has excellent heat resistance, weather resistance, corrosion resistance, abrasion resistance, electrical insulation, etc., so it can be used for lining materials such as pipes, valves, pumps, etc. It is used for various purposes such as blue tubes, films, well-known skeletons, pump impellers, mechanical parts, and chemical laboratory equipment.
- the molded article made of the fluororesin is It is difficult to apply it to parts that require high precision in the electronics field, pipes and lining materials used in chemical equipment. .
- inorganic fillers such as carbon fiber and glass fiber
- fluorine resin In order to improve the mechanical strength, deflection temperature under load, and dimensional stability of molded products, it is possible to mix inorganic fillers such as carbon fiber and glass fiber with fluorine resin. Although attempts have been made, sufficient effects cannot be obtained due to the affinity of fluororesin, such as its dispersibility and interfacial adhesion, and conversely, moldability and fluorine resin have When the excellent surface properties (non-adhesiveness, low friction, etc.) are reduced, or when recycling, the filler is easily cut. Repeated cycling causes a reduction in strength.
- Aromatic polyesters that form an anisotropic molten phase that is, liquid crystalline aromatic polyesters (hereinafter abbreviated as liquid crystal polyesters) It has been reported about compounding.
- fluorine-containing polymers have low surface energy, they generally have a problem that they have an affinity with other materials. There is. For this reason, when the fluorine resin and the liquid crystal polyester are melt-blended, phase separation occurs, and the interfacial adhesion is not practically equal.
- the liquid crystal polyester is difficult to disperse in the fluororesin when it is pre-mixed when the interface is apt to peel off, and it is added by causing aggregation. It is difficult to achieve the effect fully.
- these are substantially synthesized by utilizing the excellent affinity between PVDF and a polymer containing a carbonyl group such as an acrylic polymer.
- a non-fluorine-based compatibilizer is used, and the fluorine-containing polymer is limited to PVDF.
- the compatibilizing agent itself is inferior in chemical resistance and heat resistance to that of the main component polymer.
- it is selected to be a sufficiently effective compatibilizer when blending a perfluoro-based fluororesin with a liquid crystal polyester. Not in .
- the purpose of the present invention is to solve the above-mentioned conventional problems and Maintains excellent heat resistance, chemical resistance, weather resistance, surface properties (non-adhesive, low friction), stain resistance, electrical insulation, etc. of fluoro fluororesin.
- An object of the present invention is to provide a thermoplastic resin composition comprising a fluoropolymer and a liquid crystal polyester. Disclosure of invention
- thermoplastic resin composition of the present invention comprises:
- the methylol group-containing fluorine-containing polymer (A) has a methylol group at the end of its molecular chain, with 3 ⁇ 10 2 to 1 ⁇ 10 6 carbon atoms. It is preferable that at least one member selected from the group consisting of X 10 U perfluoropolymers is used.
- the methylol group-containing fluorine-containing polymer (A) comprises tetrafluoroethylene and a compound represented by the formula:
- the copolymer is a copolymer with at least one member selected from the group consisting of perfluoro (alkyl vinyl ether) represented by
- the copolymer contains 1 to 10% of monofluoro (alkyl vinyl ether) unit, and has a methylol group at the molecular chain terminal at a carbon number of 1X. 1 0 6 pair to 2 X 1 0 ⁇ lxl O to 3 Yes, 3 8 0 ° C 7 kg main le walk opening one record over preparative at load 1 ⁇ 1 0 0 g Z l 0 min
- at least one species is selected from the group that is the most important.
- the above-mentioned methylol group-containing fluorine-containing polymer (A) has a methylol group at the molecular chain terminal at 3 ⁇ 10 2 to 1 ⁇ 10 6 carbon atoms. X 1 0 3 or that the is not the good or Yusuke.
- the present invention was or, and from 0.1 to 4 0% (eight) a number average molecular weight 5 1 0 2 ⁇ 5 ⁇ 1 0 ⁇ main switch b Lumpur group-containing off Tsu containing polymer
- the main switch b Lumpur group-containing off Tsu containing polymer (Alpha) is a main switch b one Le group at the molecular chain end of its zero six lxl carbon atoms
- (C) has a methylol group at the end of its molecular chain having a carbon number of I X
- the present invention relates to a thermoplastic resin composition.
- methylol group-containing fluoropolymer (A) has a methylol group at the end of its molecular chain at a carbon number of 1 ⁇ 10 ° to 3 ⁇ 10 ⁇ 1.
- 10 Preferably at least one member selected from the group consisting of the inherently perfluoropolymers o
- the methylol group-containing fluorine-containing polymer (A) comprises tetrafluoroethylene and a compound represented by the formula:
- R f is a perfluoroalkyl group having 34 carbon atoms.
- a copolymer with at least one member selected from the group consisting of a fluoro (vinyl alcohol ether); and a copolymer with at least one member selected from the group consisting of coalescence viewed contains 1 to 0% the path over full O b (a Le key le vinyl Rue over Te Le) units, the number 1 X 1 0 6 carbon the main switch b Lumpur group at the molecular chain end of its 2 X 10 to 1 X 10.
- a small amount selected from the group consisting of more than 1 to 100 g Zl0 min when melted at a load of 7 kg at 380 ° C 7 kg Preferably at least one species.
- the methylol group-containing fluorine-containing polymer (A) is tetrafluoroethylene. And Tsu Oh a copolymer as one full O b (A Le key Honoré bicycloalkyl two Honoré et Ichite Le), the molecular chain terminals of that the main switch b Lumpur group number 1 X 1 0 6 carbon On the other hand, it is preferred that at least one species selected from the group consisting of more than 3 X 10 2 1 X 10 3
- the methylol group-containing fluoropolymer (A) has a formula: H-—CF 2 CF 2 ⁇ ⁇ 1 ⁇ ⁇ CH 20 H
- n is from 5 to an integer of LO 3
- BEST MODE FOR CARRYING OUT THE INVENTION The perfluoro polymer (A) containing a methylol group used in the present invention is, for example, tetrafluorophenol.
- Len homopolymer tetrafluoroethylene copolymer, hexafluoropropylene copolymer, tetrafluoroethylene copolymer Copolymer, tetrafluoroethylene-perfluoro (alkyl vinyl ether) -hexafluoropropyl It is a polymer obtained by introducing a methylol group at one or both terminals of a perfluoropolymer such as propylene terpolymer.
- the molecular weight of a fluorine-containing polymer having these methylol groups is, for example, represented by the formula:
- the concentration of the main switch b Lumpur groups in A) is a main switch b Lumpur group number against the TansoHara terminal 1 X 1 0 6 or in the polymer in its Ki out and to this I Table, Pas -When blending a fluoropolymer with a liquid crystal polyester, the methylol group concentration, which is effective for improving dispersibility and interfacial adhesion, depends on its weight. -carbon atom of the case body 1 X 1 0 and D pieces in pairs, main switch b Lumpur group 2 xl 0 ⁇ lxl 0 5 pieces, good or to rather is Ah in 3 X 1 0 ⁇ 1 X 1 0 5 or .
- the fluorine-containing polymer containing a methylol group (A) can be produced by various methods.
- a methylol group at the terminal end of the polymer by a polymer reaction after the polymerization, for example, after the polymerization.
- Polymerization was carried out using a chain transfer agent or a polymerization initiator that can easily convert the polymer end into a segment having a methylol group.
- the end of the obtained polymer can be obtained by converting it to a segment containing a methylol group by a macromolecular reaction.
- the liquid crystal polyester used in the present invention is, for example, a small number selected from the group consisting of aromatic dicarboxylic acids and alicyclic dicarboxylic acids. At least one member selected from the group consisting of aromatic, alicyclic, and aliphatic polyols; and at least one member selected from the group consisting of aromatic hydroxy.
- a liquid crystal polyester composed of at least one component selected from the group consisting of carboxylic acid is obtained. Typical combinations of these include, for example, para-hydroxybenzoic acid, biphenyldiol, and terephthalic acid as the main components.
- Mono for example, manufactured by Sumitomo Chemical Co., Ltd., trade name: Econo E200 or E600, manufactured by Nihon Petrochemical Co., Ltd., trade name: Xydar RC — FC 400 or 300, Polyplastics Manufactured by KUS Co., Ltd., trade name Vectra C Series, manufactured by Ueno Pharmaceutical Co., Ltd., trade name UENOLCP 2000, manufactured by Idemitsu Petrochemical Co., Ltd., trade name: Idemitsu LCP 300 Etc.), those containing parahydroxybenzoic acid and 6-hydroxynaphthoic acid as main components (for example, AISH, AIJIANO) VICTREXSRP, Ueno Pharmaceutical Co., Ltd., UENOLCP 100, Polyplastics Co., Ltd., Vectra A Series Products, manufactured by Mitsubishi Kasei Corporation, trade name Novaki Eureto E324, manufactured by Idemitsu Petrochemical Co., Ltd., trade name: Idemitsu LCP 300, manufactured by Unitika Ltd
- these copolymers are liquid crystal polymers.
- the optical anisotropy is confirmed by using a normal polarizing microscope. For example, place a test piece adjusted to a thickness of lmm or less on a heating stage and heat it at a heating rate of about 2 ° CZ mm in a nitrogen atmosphere. .
- the polarizer and analyzer of the polarizing microscope can be easily checked by making them orthogonal to each other and observing them at a magnification of 40 times or 100 times. .
- the temperature at which these copolymers transition to the liquid crystal phase is simultaneously increased. Measure the degree. In some cases, this can be measured by thermal analysis (eg, DSCTMA).
- the first thermoplastic resin composition of the present invention comprises:
- the above-mentioned fluoropolymer containing a methylol group (A) can be used, but the thermoplastic resin composition comprising these two components can be used for molding. and to have Oh if Ru have use, the number average molecular weight of about 1 X 1 0 5 ⁇ 5 xl 0 5, Te preparative La off Ruo b et Ji les down the introduction of the main switch b Lumpur group at the terminal Homopolymers, tetrafluoroethylene copolymers, tetrafluoroethylene copolymers, tetrafluoroethylene copolymers, tetrafluoroethylene copolymers (Rubinyl ether) copolymer, tetrafluoroethylene 1-fluoro (alkyl vinyl ether) 1-fluorofluoropropyl It is preferable to introduce a methylol group at the end of a perfluoro resin called a terpolymer, and it is preferable to use
- R f is a C 3-4 perfluoroalkyl group
- R f a group consisting of perfluoro (alkyl vinyl ether) represented by A copolymer with at least one selected from the group consisting of Fluorine-containing polymer containing 110% by weight of a fluoro (alkyl vinyl ether) unit and having a methylol group at the end of its molecular chain. Is preferred.
- the methylol group in the copolymer of tetrafluoroethylene and sulfonic acid has a carbon atom at the end of its molecular chain.
- the maleole toffee of this copolymer, 1 to: LOO g ZIO component is preferred, and 360 g / 10 minutes component is preferred. It is more preferred.
- melt flow rate is less than 1, the dispersibility in the melt-kneading operation tends to be insufficient and the molding processability of the composition tends to be reduced. If it exceeds 100, the mechanical strength of a molded article obtained from the composition tends to decrease.
- liquid crystal polyester used in these thermoplastic resin compositions the above-mentioned liquid crystal polyesters can be used.
- the perfluoro-based resins are also preferred.
- a polymer that forms an anisotropic molten phase in the above molding temperature range is preferably used.
- the composition is generally dispersed in a molten state. This is because a method that includes the step of causing the reaction to be used is used. In such a method, one of the perfluoro resin and the liquid crystal polyester constituting the composition may cause thermal decomposition. In some cases, it is not preferable because the physical properties of the obtained molded body are deteriorated.
- the methylol group-containing fluorine-containing polymer (A) can be used in combination with the tetrafluorophenol and the perfluoro (alkyl vinyl ether).
- the preferred molding temperature range of the fluorine-containing polymer alone is 300 to 400 ° C., and more preferably 320 It is up to 400 ° C, and it is possible to select a liquid crystal polyester that can be molded in such a temperature range. I like it.
- Such preferred liquid crystal polyesters include, for example, wholly aromatic polyesters, such as parahydroxybenzoic acid, bif ⁇ Those whose main components are diol diol and terephthalic acid (for example, manufactured by Sumitomo Chemical Co., Ltd., trade name: Econo E200, E600) 00 or E700, manufactured by Nippon Petrochemical Co., Ltd., trade name: Xydar RCZFC 400 or 300, manufactured by Polyplastics, Inc., product Brand name C-Series, Ueno Pharmaceutical Co., Ltd., trade name UENOLCP 2000, Idemitsu Petrochemical Co., Ltd., trade name Idemitsu LCP 300, etc.), para-hydro X-Benzoic acid, 6-Hydroxinaphthoic acid-based (for example, AI-SI Japan Ltd., trade name) VICTREXSRP, Ueno Pharmaceutical Co., Ltd.
- parahydroxybenzoic acid for example, manufactured by Sumitomo Chemical Co.,
- Para-hydroxybenzoic acid, biphenyl diol, and terephthalic acid as the main components (for example, Sumitomo Chemical Co., Ltd.)
- Product name Econole E200 or E600 manufactured by Nippon Petrochemical Co., Ltd.
- Product name Xydar RCZFC400 or 300 Polypropylene Product name: Vectra C Series, manufactured by Lasix Corporation, product name: UEN 0 LCP 2000, manufactured by Idemitsu Petrochemical Co., Ltd., product name: Ueno Pharmaceutical Co., Ltd. Idemitsu LCP 300, etc.
- UEN 0 LCP 2000 manufactured by Idemitsu Petrochemical Co., Ltd.
- thermoplastic resin composition which is composed of two components, a fluoropolymer containing a methylol group (A) and a liquid crystal polyester (B),
- the mixing ratio of (A) and (B) is 0.1 to 99% for (A), 1 to 99.9% for (B), and preferably 50 to 100 for (A).
- (B) is 1 to 50%, more preferably (A) is 60 to 97%, and (B) is 3 to 40%.
- the content of the liquid crystal polyester (B) is less than 3%, the effect of improving the mechanical strength, linear expansion coefficient, and moldability of the fluorine-containing polymer tends to decrease. When the content exceeds 40%, the improved effect converges to a substantially constant value. Conversely, the excellent fluorine-containing polymer has excellent chemical resistance, electrical insulation, and surface properties (non-adhesive, low adhesion). (Abrasion).
- thermoplastic resin composition of the present invention is the second thermoplastic resin composition of the present invention.
- thermoplastic resin composition composed of these three components does not contain a methylol group or does not contain a specific amount or less.
- a perfluoro-based resin containing a specific amount or more of a methylol group at the terminal is used.
- the fluorine-containing polymer (A) acts as a compatibilizer between (C) and (B) and is a composition having improved dispersibility and interfacial adhesion.
- the fluorine-containing polymer containing a methylol group in the composition is the part between the remaining liquid crystal polyester (B) and the perfluoro resin (C). It is thought that it works as a compatibilizer for the iron.
- the methylol group-containing perfluoropolymer (A) used in the present invention includes, for example, tetrafluoroethylene alone homopolymer, tetrafluoroethylene, and the like.
- Frou It has a methylol group introduced at the end of the mouth polymer.
- the molecular weight of a fluorine-containing polymer having these methylol groups is, for example, represented by the formula:
- the concentration of the terminal methylol group in the fluorine-containing polymer (A) containing a methylol group used in the present invention is determined based on the carbon atom in the polymer. It can be expressed in terms of the number of methylols per 6 groups.
- the effective concentration of the methylol group for improving the interfacial adhesion is 2 X 10 2 to: LX 10 0 to the number of carbon atoms IX 10 ⁇ of the polymer. five, rather than the favored Ru Oh 0 5 3 X 1 0 ⁇ ⁇ 1 ⁇ ⁇ .
- the composition has heat resistance and chemical resistance. Tends to decrease.
- the PFA used in the present invention is tetrafluoroethylene and the formula:
- the liquid crystal polyester (B) used in the three-component thermoplastic resin composition of the present invention is used in the above-mentioned two-component thermoplastic resin composition.
- a liquid crystal polyester similar to that described above can be suitably used.
- thermoplastic resin composition composed of three components, the mixing ratio of (A), (B) and (C) is such that (A) is 0. 0!: 40%, (B) Is 1 to 50%, and (C) is the remainder (however, the total amount of (A) and (C) is 50 to 99%), preferably (A) is 1 to 3%. 0%, (B) is 3 to 40%, and (C) is the balance (however, the total amount of (A) and (C) is 60 to 97%).
- liquid crystal polyester (B) is less than 1%, the effect of improving the mechanical strength, coefficient of linear expansion, and moldability of the perfluoro resin tends to be insufficient. If the content exceeds 50% (that is, the total amount of (A) and (C) is less than 50%), the perfluoro resin has excellent chemical resistance, electrical insulation, There is a tendency for the surface properties (non-adhesiveness, low friction) to decrease, etc. Methyl-containing group used as a compatibilizer between (B) and (C) If the content of the fluorine-containing polymer (A) is less than 0.1% based on the whole composition, the dispersibility of (B) and (C) and the effect of interfacial adhesion are insufficient. There is a tendency.
- the fluorine-containing polymer containing a methylol group (A) may be, for example, a compound represented by the formula: H -f CFCF 2 ⁇ T "CH 2 0 H
- the amount of 5 is preferably from 20% to less than 10% relative to the whole thermoplastic resin composition.
- R f is a perfluoroalkyl group having 34 carbon atoms.
- It consists of a fluoro (alkylvinylinoleatel) represented by It is a copolymer with at least one member selected from the group and contains 110% of units of fluoro (alkyl vinyl ether), and a polymer is added at the terminal of the molecular chain.
- Fluorine-containing polymer selected from the group whose temperature is more than 110 g / 10 min
- the fluorine-containing polymer (A) has 3 ⁇ 10 2 to 1 ⁇ 10 3 methyl groups for 1 ⁇ 10 6 methyl groups. It is favorable in terms of dispersibility and interfacial adhesiveness.
- the melt flow rate of the fluoropolymer (A) at a load of 7 kg at 380 ° C is 10 to 100. Those in the range of g Z l 0 minutes are even more preferred.
- the mesohydrate flow rate of the fluorine-containing polymer (A) is 10 minutes or more, it has an effect on the dispersibility at the time of blending with the liquid crystal polyester. Contribute to the target.
- liquid crystal polyester (B) the above-mentioned liquid crystal polyester can be suitably used, and a wholly aromatic polyester is preferred from the viewpoint of heat resistance.
- the mixing ratio of (A), (B) and (C) is preferably 0.1 to 40% for (A), preferably 1 to 30%, and 1 to 50% for (B).
- (C) is the balance (however, the total amount of (A) and (C) is 50-99%, preferably 60-97%). . If the liquid crystal polyester (B) is less than 1%, the effect of improving the mechanical strength, linear expansion coefficient, and moldability of the perfluoro resin tends to be insufficient. If it exceeds 50% (that is, the total amount of (A) and (C) is less than 50%), it has excellent chemical resistance and electrical insulation properties of the perfluoro resin. , Surface properties (non-adhesion, low friction), etc. tend to decrease.
- the fluoropolymer containing a methylol group (A) used as a compatibilizer between (B) and (C) is 0% based on the whole of the composition. If it is less than 1%, the effects of (B) and (C) on dispersibility and interfacial adhesion tend to be insufficient.
- thermoplastic resin composition comprising three components according to the present invention
- a second preferred embodiment is as follows.
- (C) molecular end in the main switch b Lumpur group or containing or not name, or the the Ah Ru PFA in against the number 1 X 1 0 6 carbon can have in I containing 2 X 1 less than zero
- (A) is 0.1 to 20%
- (B) force is 1 to 50%
- (C) is the balance (except for (B) The total amount of A) and (B) is 50 to 99%).
- composition when the composition is blended with a liquid crystal polyester (B) and a PFA (C), a methylol group as shown in (A) is used.
- Preparing an oligomer-like polymer having the above is also effective in improving the dispersibility and interfacial adhesion between (B) and (C). This is a specific example.
- oligomer-containing fluoropolymer (A) when used, if the amount of addition is too large, the mechanical properties of the composition and the durability of the composition are reduced. It is less than 20%, and more preferably less than 10%, because it tends to reduce chemical properties.
- compositions of (A :), (B) and (C) are (A) 0.5 to 10%, (B) 3 to 40%, (B) C) is the balance (however, the total amount of (A) and (C) is 60 to 97%).
- each preferred form of (B) the liquid crystal polyester and (C) the PFA is the first preferred form of the thermoplastic resin composition.
- Those similar to the contents described in the specific examples can be suitably used.
- a perfluoro resin (C) having no functional group to B
- the fluoropolymer containing methylol (A) and the perfluoro resin (C) are also in a molten state.
- Examples of the melt mixing apparatus used in the present invention include a mixing roll, a kneader mixer, a blade mixer, and an extruder.
- the extruder has a higher kneading power and can be expected to have better dispersibility when blended with a liquid crystal polyester. In that the productivity of the composition during production is good.
- the extruder one having a single axis or a screw with two or more axes can be used, but in particular, a twin-screw extruder is used.
- a composition having better dispersibility can be obtained because the kneading power is higher, and that the kneading power can be freely controlled.
- the thermoplastic resin composition of the present invention is generally in the form of a pellet, and is used as a raw material for injection molding and injection molding.
- the method of producing the pellets is not particularly limited.
- the rosin-based resin (C) can be used as a tumbler mixer, a ribbon blender, a helix mixer, a V blender, and a rocking mixer.
- the liquid crystal polyesters exemplified above usually have excellent mechanical properties (for example, strength, elastic modulus and impact) as a single molded body. Strength). Further, the molded body obtained by the injection molding or the extrusion molding is such that the polymer molecules are oriented in parallel to the flow direction of the resin when molten. It shows enhanced mechanical properties. This is an effect of self-reinforcement by the liquid crystal polymer forming an anisotropic molten phase, and the degree of the increase depends on the degree of orientation of the polymer molecule. It is controlled by That is, the mechanical properties of the melt-molded product of the liquid crystal polymer differ depending on the molding method and the shape of Z or the shape of the molded product.
- the molded product of the liquid crystal polymer exhibits remarkable anisotropy in mechanical properties.
- liquid crystal polymers usually have a very small coefficient of linear expansion (coefficient of thermal expansion) because their molecular structure is linear.
- coefficient of thermal expansion coefficient of thermal expansion
- the molded product obtained from the blend composition also has properties similar to those of the liquid crystal polyester, since the liquid crystal polyester is oriented in the fluorine resin. As a result, a certain degree of effect can be obtained in dimensional stability, moldability, and the like, as compared with a molded article made of a fluororesin alone.
- fluororesin and liquid crystal polyester have a low affinity, so when blended, they are used in blending with fluororesin. And LCD The dispersibility between the polyester and the polyester is not obvious, and it is easy to cause agglomeration.
- thermoplastic resin composition of the present invention against the main switch b Lumpur groups 1 X 1 0 D number carbon atoms in the molecular chain ends containing full Tsu containing polymer 2 1 0 2 ⁇ 1 X 1 0 5
- a simple process consisting of a fluorine-containing resin with no or few functional groups and a liquid crystal polyester is used.
- the present invention relates to a composition having improved dispersibility and interfacial adhesion, which is insufficient for a rend material.
- the molded article obtained by molding the composition of the present invention has excellent mechanical properties, dimensional stability, deflection temperature under load, molding workability, chemical resistance, surface properties, and electrical insulation properties.
- the liquid crystal polyester has an ester bond in the main chain and a hydroxyl or carboxyl group at the terminal. Therefore, by introducing a methylol group into the fluorine-containing polymer, the melt-kneading at a high temperature allows the ester of the main chain of the liquid crystal polyester to be removed.
- the ester exchange reaction occurs even partially with the tail bond, and the compatibility with each other is improved, or the introduction of a methylol group causes the polarity of the fluoropolymer to be polar. Interfacial adhesion to liquid crystal polyester without any chemical reaction. It is thought to improve dispersibility.
- thermoplastic resin composition of the present invention comprises a fluorine-containing polymer (A) having a methylol group at a terminal and a liquid crystal polyester (A).
- the resin composition of the present invention may be, for example, a glass fiber, a carbon fiber, an aramide fiber, or a glass fiber within a range that does not impair the effect.
- disulfide may contain commonly used inorganic or organic fillers such as solid lubricants such as Libden, other colorants, flame retardants, etc., and the amount of the composition may vary depending on the composition. It is usually 1 to 30% of the whole thing. In this case, the presence of unreacted methyl groups contained in the resin composition of the present invention may further enhance the effect of filling them. There is also.
- tetrafluoronorylene-perfluoro (propyl vinyl ether) copolymer (weight ratio: 95/5) was obtained. It was manufactured according to the method described in Japanese Patent Application Laid-Open No. 58-189210.
- the obtained PFA was subjected to the method described in Japanese Patent Application Laid-Open No. Hei 4 (1995) -507, and the ends of these unstable molecular chains were treated with fluorine gas and ammonia. The treatment was carried out with a gas to stabilize the terminal, and the number of terminal methyl groups was reduced to zero.
- the correction coefficient of the target end group is shown below.
- Terminal group Absorbed wave number (cm- 1 ) Correction coefficient 1 C 0 F 1 8 8 3 4 4 0 1 C 00 H 3 6 6 4 4 0-C 00 CH
- This correction factor was determined from the infrared absorption spectrum of the model compound in order to calculate the terminal group per 1 X 10 U carbon atoms.
- the infrared absorption spectrum analysis was performed using a Parkin Elmer FTIR spectrometer 1760X and NO. — Scan 100 times using a Kin Elma 1770 professional computer (both manufactured by PC-Kinma Co., Ltd.). Line
- the dioxide ( ⁇ -hydro-perforation 0 -noil) is replaced with a 12- 2 — trichlore 1 1, 2 — tri-fluorometer 1.0 g of a solution of 10% dissolved in water (R-113) was injected under pressure to initiate polymerization.
- a fluorine-containing copolymer was obtained in the same manner as in Reference Example 2, except that the methanol of 16.5 ml was used.
- the content of perfluoro (propyl vinyl ether) in the copolymer was 5.5%.
- the content of perfluoro (propyl vinyl ether) in the copolymer was 3.8%.
- ASTMD 638 according to the Tensilon Universal Testing Machine manufactured by Orientec Co., Ltd., use type 5 dampening to cross at room temperature. Measured at a speed of 1 O mm Z min.
- Example 1 507 g of PFA obtained in Reference Example 1, liquid crystal polyester (same as in Example 1) 25.4 g, and methyl obtained in Reference Example 2 were obtained. Specimens that were not kneaded and molded in the same manner except that 8.4 g of the fluoropolymer containing The test was performed in the same manner as in Example 1. Table 1 shows the test results.
- Example 1 using only the two components of 59.2 g of PFA obtained in Reference Example 1 and 25.3 g of a liquid crystal polyester (same as in Example 1) obtained in Reference Example 1 In the same manner, a test piece was kneaded and molded, and a test was performed in the same manner as in Example 1. Table 1 shows the results.
- Example 1 4.3 g of the fluorinated polymer obtained in Reference Example 4 was used instead of the methylol group-containing fluorinated polymer obtained in Reference Example 2. Except for the above, kneading and molding were performed in the same manner to obtain test pieces, and tests were performed in the same manner as in Example 1. . Table 1 shows the results.
- Example 1 In Example 1, except that 4.3 g of the fluorine-containing polymer obtained in Reference Example 5 was used instead of the methyl group-containing fluorine-containing polymer obtained in Reference Example 2 In the same manner, kneading and molding were performed in the same manner to obtain test specimens, and tests were performed in the same manner as in Example 1. Table 1 shows the results.
- the mechanical properties, dimensional stability, molding workability, deflection temperature under load, and especially the molding shrinkage and linear expansion coefficient of the perfluoro resin are representative of the perfluoro resin.
- the resulting dimensional stability is more effectively improved, and in addition, fluorocarbon resin has inherent heat resistance, chemical resistance te, resistance, surface properties (non-adhesive, low friction) Excellent performance such as stain resistance, electrical insulation and the like.
- electrical and electronic components such as connectors, chips, sockets, printed wiring boards, and auto-machining seals for automobiles Rings, shock absorbers, shields, ° Steer seals for water steering, tips for compressors on coolers It is especially useful for sliding parts of machines such as piston rings, rub rings and bearings of industrial equipment.
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1019950705772A KR100301145B1 (ko) | 1994-04-28 | 1995-04-26 | 열가소성수지조성물 |
JP52811695A JP3700178B2 (ja) | 1994-04-28 | 1995-04-26 | 熱可塑性樹脂組成物 |
US08/564,243 US5767198A (en) | 1994-04-28 | 1995-04-26 | Thermoplastic resin composition |
EP95917477A EP0709428B1 (en) | 1994-04-28 | 1995-04-26 | Thermoplastic resin composition |
DE69510637T DE69510637T2 (de) | 1994-04-28 | 1995-04-26 | Thermoplastische harzzusammensetzung |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9199494 | 1994-04-28 | ||
JP6/91994 | 1994-04-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1995029956A1 true WO1995029956A1 (fr) | 1995-11-09 |
Family
ID=14041996
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP1995/000833 WO1995029956A1 (fr) | 1994-04-28 | 1995-04-26 | Composition de resine thermoplastique |
Country Status (9)
Country | Link |
---|---|
US (1) | US5767198A (ja) |
EP (1) | EP0709428B1 (ja) |
JP (1) | JP3700178B2 (ja) |
KR (1) | KR100301145B1 (ja) |
CN (1) | CN1104466C (ja) |
CA (1) | CA2166060A1 (ja) |
DE (1) | DE69510637T2 (ja) |
RU (1) | RU2168525C2 (ja) |
WO (1) | WO1995029956A1 (ja) |
Cited By (4)
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JPH11151781A (ja) * | 1997-09-09 | 1999-06-08 | E I Du Pont De Nemours & Co | フルオロポリマー積層品 |
JP2005200542A (ja) * | 2004-01-15 | 2005-07-28 | Japan Gore Tex Inc | 接着シート |
JP2019065061A (ja) * | 2017-09-28 | 2019-04-25 | Agc株式会社 | プリント基板用樹脂組成物および製造方法 |
WO2020008923A1 (ja) * | 2018-07-02 | 2020-01-09 | 清華大学 | 含フッ素樹脂組成物およびその製造方法 |
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US6153303A (en) | 1997-08-26 | 2000-11-28 | Dupont Mitsui Fluorochemicals | Tetrafluoroethylene copolymer composition for coating metal articles |
US6166138A (en) * | 1997-09-09 | 2000-12-26 | E. I. Du Pont De Nemours And Company | Fluoropolymer composition |
US6140410A (en) * | 1997-09-09 | 2000-10-31 | E. I. Du Pont De Nemours And Company | Fluoropolymer composition |
DE19754533A1 (de) * | 1997-12-09 | 1999-06-10 | Johnson Contr Interiors Gmbh | Sonnenblendenachse |
CA2327294A1 (en) * | 1998-04-07 | 1999-10-14 | Seydel Research, Inc. | Water dispersible/redispersible hydrophobic polyester resins and their application in coatings |
JP2001088162A (ja) * | 1999-09-27 | 2001-04-03 | Du Pont Mitsui Fluorochem Co Ltd | 複合フッ素樹脂物品の成形方法 |
WO2001048280A1 (en) * | 1999-12-24 | 2001-07-05 | E.I. Dupont De Nemours And Company | Melt processible fluoropolymer composites |
JP2001181463A (ja) | 1999-12-24 | 2001-07-03 | Du Pont Mitsui Fluorochem Co Ltd | 熱溶融性フッ素樹脂複合体 |
WO2003073405A2 (en) * | 2002-02-26 | 2003-09-04 | Uni-Pixel Displays, Inc. | Enhancements to optical flat panel displays |
DE10327437A1 (de) * | 2002-06-24 | 2004-01-22 | Luk Lamellen Und Kupplungsbau Beteiligungs Kg | Hydraulisches System |
KR20050039871A (ko) * | 2002-09-03 | 2005-04-29 | 엔테그리스, 아이엔씨. | 전자 프로세싱 어플리케이션에 이용하기 위한 고온, 고강도, 착색가능한 재료 |
US20070026171A1 (en) * | 2002-09-03 | 2007-02-01 | Extrand Charles W | High temperature, high strength, colorable materials for use with electronics processing applications |
AU2003279239A1 (en) * | 2002-10-09 | 2004-05-04 | Entegris, Inc. | High temperature, high strength, colorable materials for device processing systems |
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US7379642B2 (en) | 2005-01-18 | 2008-05-27 | Adc Telecommunications, Inc. | Low shrink telecommunications cable and methods for manufacturing the same |
US7662129B2 (en) * | 2006-02-14 | 2010-02-16 | Boston Scientific Scimed, Inc. | Medical device employing liquid crystal block copolymers and method of making the same |
US7582078B2 (en) * | 2006-02-14 | 2009-09-01 | Boston Scientific Scimed, Inc. | Medical device employing liquid crystal block copolymers and method of making the same |
JP5095115B2 (ja) * | 2006-03-27 | 2012-12-12 | Ntn株式会社 | 動圧軸受装置 |
US8391658B2 (en) * | 2008-05-28 | 2013-03-05 | Adc Telecommunications, Inc. | Fiber optic cable with jacket embedded with reinforcing members |
WO2011063221A2 (en) | 2009-11-20 | 2011-05-26 | Adc Telecommunications, Inc. | Fiber optic cable |
US8915659B2 (en) | 2010-05-14 | 2014-12-23 | Adc Telecommunications, Inc. | Splice enclosure arrangement for fiber optic cables |
JP5614217B2 (ja) * | 2010-10-07 | 2014-10-29 | デクセリアルズ株式会社 | マルチチップ実装用緩衝フィルム |
US8885998B2 (en) | 2010-12-09 | 2014-11-11 | Adc Telecommunications, Inc. | Splice enclosure arrangement for fiber optic cables |
US9156973B2 (en) * | 2011-09-30 | 2015-10-13 | Saint-Gobain Performance Plastics Corporation | Meltprocessed fluoropolymer article and method for melt-processing fluoropolymers |
KR101427791B1 (ko) * | 2013-01-07 | 2014-08-08 | (주)플로닉스 | 플라스틱 펌프 제조방법 |
CN103267074B (zh) * | 2013-05-16 | 2016-03-02 | 江西元邦摩擦材料有限责任公司 | 硼酸镁与硫酸钙晶须复合协同增强型制动片 |
WO2022050378A1 (en) * | 2020-09-04 | 2022-03-10 | Daikin America, Inc. | Fluoropolymer and liquid crystal polymer blend |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57145140A (en) * | 1980-11-07 | 1982-09-08 | Ici Ltd | Ptfe composition containing anisotropic melt forming polymer |
JPS63230756A (ja) * | 1987-03-18 | 1988-09-27 | Polyplastics Co | 弗素樹脂組成物 |
JPH02110156A (ja) * | 1988-10-19 | 1990-04-23 | Sekisui Chem Co Ltd | ふっ素系樹脂成形体 |
JPH05105804A (ja) * | 1991-10-17 | 1993-04-27 | Nippon Petrochem Co Ltd | 摺動性樹脂組成物 |
JPH05230356A (ja) * | 1991-11-30 | 1993-09-07 | Hoechst Ag | 液晶コポリマーおよびフッ素熱可塑性樹脂の混合物、ならびにその使用方法 |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2571584B2 (ja) * | 1986-12-05 | 1997-01-16 | エヌティエヌ株式会社 | 潤滑性樹脂組成物 |
DE69325261T2 (de) * | 1992-12-10 | 1999-11-11 | Daikin Industries, Ltd. | Thermoplastische harzzusammensetzung |
-
1995
- 1995-04-26 CA CA002166060A patent/CA2166060A1/en not_active Abandoned
- 1995-04-26 RU RU96102768/04A patent/RU2168525C2/ru not_active IP Right Cessation
- 1995-04-26 DE DE69510637T patent/DE69510637T2/de not_active Expired - Fee Related
- 1995-04-26 CN CN95190346A patent/CN1104466C/zh not_active Expired - Fee Related
- 1995-04-26 KR KR1019950705772A patent/KR100301145B1/ko not_active IP Right Cessation
- 1995-04-26 EP EP95917477A patent/EP0709428B1/en not_active Expired - Lifetime
- 1995-04-26 WO PCT/JP1995/000833 patent/WO1995029956A1/ja active Application Filing
- 1995-04-26 JP JP52811695A patent/JP3700178B2/ja not_active Expired - Fee Related
- 1995-04-26 US US08/564,243 patent/US5767198A/en not_active Expired - Lifetime
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57145140A (en) * | 1980-11-07 | 1982-09-08 | Ici Ltd | Ptfe composition containing anisotropic melt forming polymer |
JPS63230756A (ja) * | 1987-03-18 | 1988-09-27 | Polyplastics Co | 弗素樹脂組成物 |
JPH02110156A (ja) * | 1988-10-19 | 1990-04-23 | Sekisui Chem Co Ltd | ふっ素系樹脂成形体 |
JPH05105804A (ja) * | 1991-10-17 | 1993-04-27 | Nippon Petrochem Co Ltd | 摺動性樹脂組成物 |
JPH05230356A (ja) * | 1991-11-30 | 1993-09-07 | Hoechst Ag | 液晶コポリマーおよびフッ素熱可塑性樹脂の混合物、ならびにその使用方法 |
Non-Patent Citations (1)
Title |
---|
See also references of EP0709428A4 * |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH11151781A (ja) * | 1997-09-09 | 1999-06-08 | E I Du Pont De Nemours & Co | フルオロポリマー積層品 |
JP2005200542A (ja) * | 2004-01-15 | 2005-07-28 | Japan Gore Tex Inc | 接着シート |
JP4598408B2 (ja) * | 2004-01-15 | 2010-12-15 | ジャパンゴアテックス株式会社 | 接着シート |
JP2019065061A (ja) * | 2017-09-28 | 2019-04-25 | Agc株式会社 | プリント基板用樹脂組成物および製造方法 |
WO2020008923A1 (ja) * | 2018-07-02 | 2020-01-09 | 清華大学 | 含フッ素樹脂組成物およびその製造方法 |
JPWO2020008923A1 (ja) * | 2018-07-02 | 2021-03-11 | 清華大学 | 含フッ素樹脂組成物およびその製造方法 |
Also Published As
Publication number | Publication date |
---|---|
EP0709428B1 (en) | 1999-07-07 |
RU2168525C2 (ru) | 2001-06-10 |
US5767198A (en) | 1998-06-16 |
DE69510637T2 (de) | 1999-12-02 |
CN1127515A (zh) | 1996-07-24 |
EP0709428A4 (en) | 1996-10-23 |
KR100301145B1 (ko) | 2001-11-05 |
CA2166060A1 (en) | 1995-11-09 |
JP3700178B2 (ja) | 2005-09-28 |
KR960703153A (ko) | 1996-06-19 |
CN1104466C (zh) | 2003-04-02 |
DE69510637D1 (de) | 1999-08-12 |
EP0709428A1 (en) | 1996-05-01 |
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