WO2016010127A1 - フィルム及びその製造方法 - Google Patents
フィルム及びその製造方法 Download PDFInfo
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- WO2016010127A1 WO2016010127A1 PCT/JP2015/070457 JP2015070457W WO2016010127A1 WO 2016010127 A1 WO2016010127 A1 WO 2016010127A1 JP 2015070457 W JP2015070457 W JP 2015070457W WO 2016010127 A1 WO2016010127 A1 WO 2016010127A1
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- WIPO (PCT)
- Prior art keywords
- film
- fluororesin
- resin
- aromatic
- mechanical strength
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F14/00—Homopolymers and 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
- C08F14/18—Monomers containing fluorine
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/20—Manufacture of shaped structures of ion-exchange resins
- C08J5/22—Films, membranes or diaphragms
- C08J5/2206—Films, membranes or diaphragms based on organic and/or inorganic macromolecular compounds
- C08J5/2218—Synthetic macromolecular compounds
- C08J5/2231—Synthetic macromolecular compounds based on macromolecular compounds obtained by reactions involving unsaturated carbon-to-carbon bonds
- C08J5/2243—Synthetic macromolecular compounds based on macromolecular compounds obtained by reactions involving unsaturated carbon-to-carbon bonds obtained by introduction of active groups capable of ion-exchange into compounds of the type C08J5/2231
- C08J5/225—Synthetic macromolecular compounds based on macromolecular compounds obtained by reactions involving unsaturated carbon-to-carbon bonds obtained by introduction of active groups capable of ion-exchange into compounds of the type C08J5/2231 containing fluorine
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
- C08L71/08—Polyethers derived from hydroxy compounds or from their metallic derivatives
- C08L71/10—Polyethers derived from hydroxy compounds or from their metallic derivatives from phenols
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- G—PHYSICS
- G10—MUSICAL INSTRUMENTS; ACOUSTICS
- G10K—SOUND-PRODUCING DEVICES; METHODS OR DEVICES FOR PROTECTING AGAINST, OR FOR DAMPING, NOISE OR OTHER ACOUSTIC WAVES IN GENERAL; ACOUSTICS NOT OTHERWISE PROVIDED FOR
- G10K13/00—Cones, diaphragms, or the like, for emitting or receiving sound in general
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- H—ELECTRICITY
- H04—ELECTRIC COMMUNICATION TECHNIQUE
- H04R—LOUDSPEAKERS, MICROPHONES, GRAMOPHONE PICK-UPS OR LIKE ACOUSTIC ELECTROMECHANICAL TRANSDUCERS; DEAF-AID SETS; PUBLIC ADDRESS SYSTEMS
- H04R7/00—Diaphragms for electromechanical transducers; Cones
- H04R7/02—Diaphragms for electromechanical transducers; Cones characterised by the construction
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2500/00—Characteristics or properties of obtained polyolefins; Use thereof
- C08F2500/12—Melt flow index or melt flow ratio
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2650/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G2650/28—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the polymer type
- C08G2650/38—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the polymer type containing oxygen in addition to the ether group
- C08G2650/40—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the polymer type containing oxygen in addition to the ether group containing ketone groups, e.g. polyarylethylketones, PEEK or PEK
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2371/00—Characterised by the use of polyethers obtained by reactions forming an ether link in the main chain; Derivatives of such polymers
- C08J2371/08—Polyethers derived from hydroxy compounds or from their metallic derivatives
- C08J2371/10—Polyethers derived from hydroxy compounds or from their metallic derivatives from phenols
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2427/00—Characterised by the use 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; Derivatives of such polymers
- C08J2427/02—Characterised by the use 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; Derivatives of such polymers not modified by chemical after-treatment
- C08J2427/12—Characterised by the use 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; Derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
- C08J2427/18—Homopolymers or copolymers of tetrafluoroethylene
Definitions
- the present invention relates to a film and a manufacturing method thereof.
- Engineering plastics such as aromatic polyetherketone resins are thermoplastic resins having high heat resistance and high mechanical strength and dimensional stability, and are therefore used in various applications.
- fluororesins are excellent in properties such as slidability, heat resistance, chemical resistance, solvent resistance, weather resistance, flexibility, electrical properties, etc., and are widely used in automobiles, industrial machines, OA equipment, electrical and electronic equipment, etc. Used in the field. However, it is often inferior to physical heat resistance as indicated by mechanical properties and deflection temperature under load compared to crystalline heat-resistant thermoplastic resin, and dimensions compared to amorphous heat-resistant thermoplastic resin. The situation is inferior to stability, and the range of use is limited.
- Patent Document 1 discloses a resin composition containing an aromatic polyether ketone resin (I) and a fluororesin (II) for the purpose of obtaining a molded product having a low dynamic friction coefficient and a high limit PV value.
- the fluororesin (II) is a copolymer of tetrafluoroethylene and a specific perfluoroethylenically unsaturated compound, and the mass ratio of the aromatic polyetherketone resin (I) to the fluororesin (II) (I) / (II) is 95: 5 to 50:50, melt viscosity ratio (I) / (II) is 0.3 to 5.0, and fluororesin (II) is aromatic polyetherketone resin (I) A resin composition is described which is dispersed in the form of particles and has an average dispersed particle size of fluororesin (II) of less than 3.0 ⁇ m.
- Patent Document 2 discloses an insulated wire having a conductor (A) and an insulating layer (B) formed on the outer periphery of the conductor (A), and the insulating layer (B) is an aromatic polyetherketone resin.
- An aromatic polyether ketone resin formed from a resin composition comprising (I) and a fluororesin (II), wherein the fluororesin (II) is a copolymer of tetrafluoroethylene and a specific perfluoroethylenically unsaturated compound
- An insulated wire characterized in that the melt viscosity ratio (I) / (II) between (I) and fluororesin (II) is 0.3 to 5.0 is described.
- the conventional film formed from the resin composition containing the aromatic polyetherketone resin (I) and the fluororesin (II) has not been sufficient in abrasion resistance.
- the mechanical strength required for a speaker vibration film or the like is not sufficient, and a film having both excellent mechanical strength and wear resistance has not been obtained.
- This invention is made
- the present invention is a film containing an aromatic polyether ketone resin (I) and a fluororesin (II), wherein the aromatic polyether ketone resin (I) has a crystallinity of 10% or more. It is a film.
- the mass ratio (I) :( II) of the aromatic polyether ketone resin (I) to the fluororesin (II) is preferably 40:60 to 99: 1.
- the fluororesin (II) is preferably dispersed in the form of particles in the aromatic polyetherketone resin (I).
- the average dispersed particle size of the fluororesin (II) in the aromatic polyetherketone resin (I) is preferably 3.0 ⁇ m or less.
- the film of the present invention preferably has a melt viscosity ratio (I) / (II) of the aromatic polyether ketone resin (I) and the fluororesin (II) of 0.01 to 5.0.
- the fluororesin (II) preferably has a melt flow rate of 0.1 to 100 g / 10 min.
- the aromatic polyether ketone resin (I) is preferably a polyether ether ketone.
- the present invention is also a speaker diaphragm including the film.
- the present invention is also a thrust washer including the above film.
- the film of this invention is excellent in mechanical strength and abrasion resistance by having the said structure. Moreover, the speaker diaphragm of the present invention is excellent in acoustic characteristics.
- the film of the present invention is a film containing an aromatic polyether ketone resin (I) and a fluororesin (II), and the crystallinity of the aromatic polyether ketone resin (I) is 10% or more.
- the mechanical strength and the abrasion resistance are remarkably improved when the crystallinity of the aromatic polyetherketone resin (I) is 10% or more.
- the film of the present invention also has excellent elongation properties despite having excellent mechanical strength and abrasion resistance. The present invention is described in detail below.
- the film of the present invention contains an aromatic polyether ketone resin (I) and a fluororesin (II).
- the crystallinity of the aromatic polyether ketone resin (I) is 10% or more.
- the mechanical strength of the film is remarkably improved, and furthermore, the film has excellent wear resistance.
- the crystallinity is preferably 12% or more, more preferably 13% or more, and further preferably 15% or more. It is preferably 17% or more, particularly preferably 19% or more.
- the said crystallinity degree is 30% or less. More preferably, it is 25% or less.
- the crystallinity is the crystallinity of the aromatic polyetherketone resin (I) in the film, and does not mean the crystallinity of the aromatic polyetherketone resin (I) as a raw material.
- the crystallinity can be obtained by the following equation by measuring wide-angle X-ray diffraction in a scanning angle range of 5 to 40 degrees using an X-ray diffractometer.
- Crystallinity (%) 100 ⁇ (peak area derived from crystal of aromatic polyetherketone resin (I)) / (total peak area) More specifically, using an Ultimate III X-ray diffractometer manufactured by RIGAKU, wide-angle X-ray diffraction was measured in an output range of 40 kV to 40 mA and a scanning angle of 5 to 40 degrees, and analysis software RADEKU JADE 6.0 was used. The peak area derived from the crystals of the aromatic polyetherketone resin (I) and the total peak area can be calculated, and the crystallinity can be calculated from the above formula.
- the total peak area is an area obtained by integrating the total diffraction intensities measured in a scanning angle range of 5 to 40 degrees (excluding the peak area derived from the fluororesin (II) crystal).
- the peak area derived from the crystals of the aromatic polyether ketone resin (I) is the total area of the peaks derived from the crystals of the aromatic polyether ketone resin (I).
- the peak derived from the crystal of the aromatic polyetherketone resin (I) varies depending on the type thereof.
- the degree of crystallinity of the fluororesin (II) is preferably 30 to 35%.
- the film of the present invention is excellent in mechanical strength, abrasion resistance and elongation characteristics.
- the degree of crystallinity of the fluororesin (II) is calculated in the same manner as the aromatic polyetherketone resin (I) by calculating the peak area derived from the fluororesin (II) crystal and the entire peak area, Can be sought.
- Crystallinity (%) 100 ⁇ (peak area derived from crystal of fluororesin (II)) / (total peak area)
- the total peak area is the sum of the intensities measured in the scanning angle range of 5 to 40 degrees (except for the peak area derived from the aromatic polyetherketone resin (I) crystal).
- the peak area derived from the fluororesin (II) crystal is the sum of the peak areas derived from the fluororesin (II) crystal.
- the aromatic polyether ketone resin (I) is preferably at least one resin selected from the group consisting of polyether ketone, polyether ether ketone, polyether ketone ketone and polyether ketone ether ketone ketone. More preferred is at least one resin selected from the group consisting of polyetherketone and polyetheretherketone, and even more preferred is polyetheretherketone.
- the aromatic polyether ketone resin (I) preferably has a melt viscosity of 0.25 to 1.50 kNsm ⁇ 2 at 60 sec ⁇ 1 and 390 ° C.
- the melt viscosity is in the above range, the processing characteristics are improved, and further, a film having excellent mechanical strength and wear resistance can be obtained.
- a more preferred lower limit for the melt viscosity is 0.80 kNsm -2 .
- a more preferable upper limit of the melt viscosity is 1.30 kNsm ⁇ 2 .
- the melt viscosity of the aromatic polyether ketone resin (I) is measured according to ASTM D3835.
- the aromatic polyether ketone resin (I) preferably has a glass transition temperature of 130 ° C. or higher. More preferably, it is 135 degreeC or more, More preferably, it is 140 degreeC or more. When the glass transition temperature is in the above range, a film having excellent heat resistance can be obtained. The glass transition temperature is measured by a differential scanning calorimetry (DSC) apparatus.
- DSC differential scanning calorimetry
- the aromatic polyether ketone resin (I) preferably has a melting point of 300 ° C. or higher. More preferably, it is 320 degreeC or more. When the melting point is in the above range, the heat resistance of the film can be improved. The melting point is measured by a differential scanning calorimetry (DSC) apparatus.
- DSC differential scanning calorimetry
- the fluororesin (II) is preferably a melt-processable fluororesin, such as tetrafluoroethylene / perfluoroethylenically unsaturated compound copolymer, ethylene / tetrafluoroethylene copolymer, polychlorotrifluoroethylene. Chlorotrifluoroethylene / tetrafluoroethylene copolymer, ethylene / chlorotrifluoroethylene copolymer, tetrafluoroethylene / vinylidene fluoride copolymer, at least one selected from the group consisting of polyvinylidene fluoride and polyvinyl fluoride More preferably it is a seed.
- a melt-processable fluororesin such as tetrafluoroethylene / perfluoroethylenically unsaturated compound copolymer, ethylene / tetrafluoroethylene copolymer, polychlorotrifluoroethylene. Chlorotrifluor
- fluororesin (II) 1 type may be used and 2 or more types may be used.
- Rf 1 is —ORf 2
- Rf 2 is preferably a perfluoroalkyl group having 1 to 3 carbon atoms.
- hexafluoropropylene and perfluoro alkyl It is preferably at least one selected from the group consisting of vinyl ethers). More preferably, it is at least one selected from the group consisting of hexafluoropropylene, perfluoro (methyl vinyl ether), perfluoro (ethyl vinyl ether) and perfluoro (propyl vinyl ether), more preferably hexafluoropropylene and perfluoro It is at least one selected from the group consisting of fluoro (propyl vinyl ether). Particularly preferred is hexafluoropropylene.
- the fluororesin (II) is preferably composed of 80 to 99.5 mol% of TFE and 0.5 to 20 mol% of a perfluoroethylenically unsaturated compound represented by the general formula (1). .
- the lower limit of the content of TFE constituting the fluororesin (II) is more preferably 85 mol%, further preferably 87 mol%, particularly preferably 90 mol%, and particularly preferably 93 mol%.
- the upper limit of the content of TFE constituting the fluororesin (II) is more preferably 97 mol%, still more preferably 95 mol%.
- the lower limit of the content of the perfluoroethylenically unsaturated compound represented by the general formula (1) constituting the fluororesin (II) is more preferably 1 mol%, further preferably 1.5 mol%. 4 mol% is particularly preferred.
- the upper limit of the content of the perfluoroethylenically unsaturated compound represented by the general formula (1) constituting the fluororesin (II) is more preferably 15 mol%, further preferably 13 mol%, and more preferably 10 mol%. Is particularly preferred.
- the fluororesin (II) is preferably a perfluoropolymer because a film having better mechanical strength and abrasion resistance can be obtained.
- the fluororesin (II) is composed of a tetrafluoroethylene / perfluoro (alkyl vinyl ether) copolymer, a tetrafluoroethylene / hexafluoropropylene copolymer, and a tetrafluoroethylene / hexafluoropropylene / perfluoro (alkyl vinyl ether) copolymer.
- the fluororesin (II) is also a tetrafluoroethylene / hexafluoropropylene / monomer ⁇ copolymer having a tetrafluoroethylene / hexafluoropropylene / monomer ⁇ molar ratio of 80 to 98.5.
- a copolymer having a ratio of /1.5 to 20/0 to 0.9 is also preferable.
- the fluororesin (II) is the above copolymer, it is easy to disperse the fluororesin (II) in the form of fine particles in the aromatic polyetherketone resin (I).
- mechanical strength and wear resistance can be further improved.
- the copolymer is superior in that it exhibits these effects as compared with a tetrafluoroethylene / perfluoro (alkyl vinyl ether) copolymer containing 1 mol% or more of perfluoro (alkyl vinyl ether).
- the monomer ⁇ is a monomer copolymerizable with tetrafluoroethylene and hexafluoropropylene. Examples of the monomer ⁇ include perfluoro (alkyl vinyl ether).
- the fluororesin (II) preferably has a melt viscosity of 0.3 to 3.0 kNsm -2 at 60 sec -1 and 390 ° C.
- the melt viscosity is in the above range, the processing characteristics are improved, and a film having more excellent mechanical strength and wear resistance can be obtained.
- a more preferable lower limit of the melt viscosity is 0.4 kNsm ⁇ 2 .
- the upper limit of the melt viscosity is more preferably 2.5 kNsm -2 , further preferably 2.0 kNsm -2 .
- the melt viscosity of the fluororesin (II) is measured according to ASTM D3835.
- the fluororesin (II) preferably has a melt flow rate (MFR) measured at 372 ° C. under a load of 5000 g of 0.1 to 100 g / 10 min, preferably 5 to 40 g / 10 min. More preferably, it is 10 to 40 g / 10 min.
- MFR melt flow rate
- a particularly preferred lower limit of MFR is 12 g / 10 minutes, and a particularly preferred lower limit is 15 g / 10 minutes.
- the particularly preferred upper limit of MFR is 38 g / 10 minutes, and the particularly preferred upper limit is 35 g / 10 minutes.
- the MFR of the fluororesin (II) is measured using a melt indexer according to ASTM D3307-01.
- the melting point of the fluororesin (II) is not particularly limited, but it is preferable in molding that the fluororesin (II) is already melted at a temperature at which the aromatic polyetherketone resin (I) used in molding is melted.
- the temperature is preferably not higher than the melting point of the aromatic polyether ketone resin (I).
- the melting point of the fluororesin (II) is preferably 230 to 350 ° C.
- the melting point of the fluororesin (II) is determined as a temperature corresponding to the maximum value in the heat of fusion curve when the temperature is raised at a rate of 10 ° C./min using a differential scanning calorimetry (DSC) apparatus.
- DSC differential scanning calorimetry
- the fluororesin (II) may be treated with fluorine gas by a known method or may be treated with ammonia.
- the film of the present invention has a melt viscosity ratio (I) / (II) of the aromatic polyetherketone resin (I) and the fluororesin (II).
- (Aromatic polyether ketone resin (I) / fluororesin (II)) is preferably 0.01 to 5.0.
- the melt viscosity ratio (I) / (II) is more preferably 0.1 to 4.0, still more preferably 0.3 to 3.0, and 0.5 to 2.5. Is particularly preferred.
- the mass ratio (I) :( II) of the aromatic polyether ketone resin (I) to the fluororesin (II) is preferably 40:60 to 99: 1. If the content of the fluororesin (II) exceeds 60 by mass ratio with the aromatic polyetherketone resin (I), the strength tends to be inferior, and if it is less than 1, the wear resistance may be reduced. . A more preferred range is 50:50 to 95: 5, and a further preferred range is 60:40 to 90:10.
- the fluororesin (II) is preferably dispersed in the form of particles in the aromatic polyetherketone resin (I).
- the film has excellent mechanical strength and abrasion resistance.
- the average dispersed particle size of the fluororesin (II) is preferably 3.0 ⁇ m or less.
- the average dispersed particle size is 3.0 ⁇ m or less, a film having excellent moldability and further excellent mechanical strength and wear resistance is obtained. If the average dispersed particle size is too large, sufficient mechanical strength and wear resistance may not be obtained. Since a film having better mechanical strength and wear resistance can be obtained and the moldability is excellent, the average dispersed particle size of the fluororesin (II) is 2.0 ⁇ m or less. Is more preferably 1.0 ⁇ m or less, and particularly preferably 0.3 ⁇ m or less. The lower limit of the average dispersed particle size is not particularly limited, but may be 0.01 ⁇ m.
- the maximum dispersed particle size of the fluororesin (II) is preferably 10 ⁇ m or less.
- the maximum dispersed particle size is 10 ⁇ m or less, mechanical strength and wear resistance are improved. Since the moldability becomes better and the mechanical strength and wear resistance are improved, the maximum dispersed particle size of the fluororesin (II) is more preferably 5 ⁇ m or less, and further preferably 1 ⁇ m or less.
- the thickness is preferably 0.5 ⁇ m or less.
- the average dispersed particle size and the maximum dispersed particle size of the fluororesin (II) are obtained by observing the film of the present invention with a confocal laser microscope or by cutting an ultrathin section from a press sheet produced from the film of the present invention.
- the ultrathin section can be obtained by performing microscopic observation with a transmission electron microscope (TEM) and binarizing the obtained image with an optical analyzer.
- TEM transmission electron microscope
- the film of this invention contains aromatic polyether ketone resin (I) and fluororesin (II), it may contain the other component as needed.
- Fibrous reinforcement materials such as whisker, such as potassium titanate, glass fiber, asbestos fiber, carbon fiber, ceramic fiber, potassium titanate fiber, aramid fiber, and other high-strength fibers
- Inorganic fillers such as calcium carbonate, talc, mica, clay, carbon powder, graphite and glass beads; colorants; inorganic or organic fillers usually used such as flame retardants; stabilizers such as minerals and flakes; silicone oil Lubricants such as molybdenum disulfide; pigments; conductive agents such as carbon black; impact resistance improvers such as rubber; and other additives.
- the film of this invention can be manufactured by the manufacturing method including the shaping
- the said resin composition can be manufactured on normal conditions using mixers, such as a compounding mill normally used in order to prepare the composition for shaping
- mixers such as a compounding mill normally used in order to prepare the composition for shaping
- Examples of the method for producing the resin composition include a method in which the aromatic polyether ketone resin (I) and the fluororesin (II) are mixed in a molten state.
- a resin composition having a desired dispersion state can be obtained by sufficiently kneading the aromatic polyether ketone resin (I) and the fluororesin (II). Since the dispersion state affects the mechanical strength and abrasion resistance of the film, and the moldability, the kneading method is appropriately selected so that a desired dispersion state is obtained in the film obtained from the resin composition. Should be.
- the aromatic polyetherketone resin (I) and the fluororesin (II) are introduced into a mixer at an appropriate ratio, and the other components are added as desired.
- the other components include a method of producing by melting and kneading at a melting point of (I) and (II).
- the other components may be added to the aromatic polyether ketone resin (I) and the fluororesin (II) in advance and mixed, or the aromatic polyether ketone resin (I) and the fluororesin (II). You may add when mix
- the temperature at the time of the melt kneading may be appropriately set depending on the kind of the aromatic polyetherketone resin (I) and the fluororesin (II) to be used, but is preferably 340 to 400 ° C., for example.
- the kneading time is usually 1 minute to 30 minutes.
- the temperature at which the resin composition is molded is preferably 340 ° C. or higher.
- the molding temperature is preferably a temperature lower than the lower one of the decomposition temperature of the fluororesin (II) and the decomposition temperature of the aromatic polyether ketone resin (I).
- Such a molding temperature is preferably 340 to 400 ° C., for example, and more preferably 360 to 400 ° C. It is preferable that the said formation process cools the shape
- Examples of the method for molding the resin composition include melt extrusion molding, calendar molding, press molding, casting molding, and the like depending on the type, application, shape, and the like of the target film. From the viewpoint of obtaining a uniform thin film, melt extrusion molding is preferred.
- the melt extrusion molding can be performed, for example, by using a T-die film molding machine to melt the resin composition, discharging the melted film from the die, and then winding it with a cooling roll.
- the cylinder temperature of the T-die film molding machine can be set within a range where the resin composition is melted, but can be molded at, for example, 340 to 400 ° C.
- the set temperature of the cooling roll can be arbitrarily set, but is preferably in the range of 150 to 270 ° C., and more preferably in the range of 180 to 220 ° C. When the set temperature of the cooling roll is less than 150 ° C. or exceeds 270 ° C., the crystallinity in the film of the resin composition may not increase.
- the time for which the molten film discharged from the die contacts the cooling roll can be adjusted, for example, in the range of 1 to 30 seconds.
- the manufacturing method preferably includes a step of subjecting the film obtained by molding to a heat treatment (annealing treatment) for the purpose of further crystallizing the film.
- the heat treatment can be performed, for example, by placing the film in a mold, placing the entire mold in an oven, and heating.
- the heating temperature is preferably in the range of 150 to 270 ° C. and more preferably in the range of 180 to 220 ° C. in order to promote crystallization.
- the heating time can be set to 0.05 to 100 hours, for example.
- a film having a crystallinity of the aromatic polyetherketone resin (I) of 10% or more can be produced by film formation under the above conditions, and in some cases, further heat treatment.
- the thickness of the film of the present invention may be appropriately set depending on the intended use and the like, but is usually 0.001 to 1 mm. From the viewpoint of ease of handling, the thickness of the film is preferably 0.01 mm or more, and more preferably 0.05 mm or more. Moreover, it is preferable that it is 0.7 mm or less, and it is more preferable that it is 0.5 mm or less.
- the film of the present invention has excellent mechanical strength and abrasion resistance, as well as heat resistance, chemical resistance, solvent resistance, strength, rigidity, low chemical permeability, dimensional stability, flame resistance, and electrical properties.
- it since it is excellent in durability, it can be used in various applications.
- speaker diaphragm film, thrust washer, connector, printed circuit board, wire wrapping film, insulation bag, insulation tape, RFID cover, battery protection film, spacer film, bearing, membrane switch, release film, etc. Can be suitably used.
- it is suitable as a diaphragm film for a speaker, a film for a thrust washer, and the like.
- the speaker diaphragm of the present invention includes the above film.
- Conventional speaker diaphragms are easily broken, and there is a need for improved mechanical strength.
- a speaker diaphragm having excellent acoustic characteristics and excellent mechanical strength has not been obtained.
- the vibration for the speaker is obtained.
- the present invention has been completed by finding that the plate has excellent mechanical properties while also having excellent mechanical strength due to the mechanical strength of the film.
- the present invention has an unknown attribute that it has excellent mechanical strength and excellent flexibility, and includes not only acoustic characteristics but also mechanical strength by including a film having the above specific configuration. And the present invention has been found to be particularly suitable for use in speaker diaphragms.
- the speaker diaphragm of the present invention is used as a diaphragm (a diaphragm) of a speaker, an earphone or the like.
- the present invention is also a speaker or an earphone including the speaker diaphragm.
- the speaker diaphragm of the present invention usually has a thickness of 10 to 100 ⁇ m.
- the speaker diaphragm of the present invention may be composed of only the above film, or may have a laminated structure of two or more layers composed of another base material and the above film. From the viewpoint of vibration damping, the speaker diaphragm of the present invention is preferably such that the film is laminated on one side or both sides of another substrate, and the film is laminated on both sides of the other substrate. Those having a three-layer structure are more preferable. When the speaker diaphragm of the present invention has the above three-layer structure, the frequency characteristics are particularly stable.
- the thickness of the other substrate is 5 to 50 ⁇ m, and the thickness of the film provided on both surfaces of the other substrate is 2 It is preferable that the thickness is ⁇ 20 ⁇ m.
- a base material made of polyimide, polyamideimide, polyetherimide, polyethylene naphthalate, polyethylene terephthalate, urethane polymer, etc. Is mentioned.
- the thrust washer of the present invention includes the above film.
- the conventional thrust washer has the problem that it is easily broken and easily worn at high loads.
- the thrust washer of the present invention has excellent mechanical strength and wear resistance by including the above film.
- the above problems can be solved.
- one having the above-mentioned film on the surface of a thrust washer-shaped molded body can be mentioned.
- the material for the thrust washer-shaped molded body those generally used as a material for a thrust washer can be used, and examples thereof include a base material made of polyoxymethylene, polyphenylene sulfide, polyamide or the like.
- Crystallinity 100 ⁇ (peak area derived from crystal of aromatic polyetherketone resin (1) / (total peak area)
- the total peak area is an area obtained by integrating all diffraction intensities measured in a scanning angle range of 5 to 40 degrees (excluding the peak area derived from the fluororesin (2) crystal).
- the peak area derived from the crystals of the aromatic polyether ketone resin (1) is the total area of the peaks derived from the crystals of the aromatic polyether ketone resin (1).
- melt viscosity of the aromatic polyetherketone resin was measured at 60 sec ⁇ 1 and 390 ° C. according to ASTM D3835.
- the melt viscosity of the fluororesin was measured at 60 sec ⁇ 1 and 390 ° C. in accordance with ASTM D3835.
- Aromatic polyetherketone resin (1) and fluororesin (2) are premixed in the proportions (parts by mass) shown in Table 1, and using a twin screw extruder, the cylinder temperature is 390 ° C. and the screw rotation speed is 300 rpm.
- the resin composition was manufactured by melt-kneading under the conditions.
- the obtained pellets of the resin composition were supplied to a T-die extruder for film molding, and were subjected to conditions of a cylinder temperature of 380 ° C., a die temperature of 380 ° C., a screw rotation speed of 7 rpm, and a temperature condition of the cooling roll shown in Table 1.
- a film having a thickness of 25 ⁇ m was formed.
- the extruded film contacts the cooling roll for 1 to 10 seconds.
- the film formed with a cooling roll set at 100 ° C. was subjected to crystallization treatment under the annealing conditions shown in Table 1. Specifically, the molded film was sandwiched between 120 mm ⁇ molds, placed in an oven at 220 ° C. for 0.1 to 3 hours, and annealed. Thereafter, using the obtained film, the crystallinity of the aromatic polyetherketone resin (1) (PEEK), the tensile modulus of elasticity of the film, the tensile elongation at break, the upper yield point stress, the wear amount, the dynamic friction coefficient, the acoustic effect was measured.
- PEEK aromatic polyetherketone resin
- the degree of crystallinity of a film obtained by annealing a fluororesin (2) single film in the same manner as the film of the example was determined in the same manner as the aromatic polyether ketone resin (1), the fluororesin (2) single film The crystallinity of was 30-35%. From this result, in the films obtained in Examples 1 to 8, the degree of crystallinity of the fluororesin (2) is estimated to be 30 to 35%.
- Comparative Examples 1 and 2 Except that the film taken out was not annealed in the oven, a film was prepared in the same manner as in Example 1, and then the obtained film was used to obtain the crystallinity of PEEK, the tensile modulus of elasticity of the film, the tensile elongation at break, Upper yield point stress, wear, dynamic friction coefficient, and acoustic effect were measured.
- the film of the present invention has excellent mechanical strength and wear resistance, it can be suitably used particularly as a film constituting a speaker diaphragm, a thrust washer, and the like.
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Abstract
Description
CF2=CF-Rf1 (1)
(式中、Rf1は、-CF3又は-ORf2を表す。Rf2は、炭素数1~5のパーフルオロアルキル基を表す。)で表されるパーフルオロエチレン性不飽和化合物の共重合体であることが好ましい。
本発明のフィルムは、芳香族ポリエーテルケトン樹脂(I)の結晶化度が10%以上であることによって、機械的強度及び耐磨耗性が著しく向上する。
本発明のフィルムは、更に、優れた機械的強度及び耐磨耗性を有するにも関わらず、優れた伸び特性をも有している。
以下に本発明を詳述する。
また、フィルムの伸び特性が優れることから、上記結晶化度は、30%以下であることが好ましい。より好ましくは、25%以下である。
なお、上記結晶化度は、フィルム中の芳香族ポリエーテルケトン樹脂(I)の結晶化度であり、原料の芳香族ポリエーテルケトン樹脂(I)の結晶化度を意味するものではない。
上記結晶化度は、X線回折装置を用い、走査角5~40度の範囲で広角X線回折を測定し、下記式により求めることができる。
結晶化度(%)=100×(芳香族ポリエーテルケトン樹脂(I)の結晶に由来するピーク面積)/(全体のピーク面積)
より具体的には、RIGAKU社製UltimaIII X線回折装置を用い、出力40kV-40mA、走査角5~40度の範囲で広角X線回折を測定し、解析ソフト RIGAKU社製 JADE6.0を用いて、芳香族ポリエーテルケトン樹脂(I)の結晶に由来するピーク面積及び全体のピーク面積を算出し、上記式から結晶化度を算出することができる。
上記全体のピーク面積は、走査角5~40度の範囲で測定した全回折強度を積算した面積(但し、フッ素樹脂(II)の結晶に由来するピーク面積は除く)である。
フッ素樹脂(II)の結晶に由来するピーク面積は、例えば、2θ=17.7度付近に観察されるピークの面積である。
芳香族ポリエーテルケトン樹脂(I)の結晶に由来するピーク面積は、芳香族ポリエーテルケトン樹脂(I)の結晶に由来するピークの面積を合計した面積である。
芳香族ポリエーテルケトン樹脂(I)の結晶に由来するピークは、その種類によって異なるが、例えば、芳香族ポリエーテルケトン樹脂(I)がポリエーテルエーテルケトン(PEEK)である場合、PEEKの結晶に由来するピーク面積は、2θ=18.7度、20.4度、22.3度及び28.6度付近に観察されるピークの面積の合計である。2θ=18.7度付近に観察されるピークは(110)面に由来するピークであり、2θ=20.4度付近に観察されるピークは(111)面に由来するピークであり、2θ=22.3度付近に観察されるピークは(200)面に由来するピークであり、2θ=28.6度付近に観察されるピークは(211)面に由来するピークであると推測される。
結晶化度(%)=100×(フッ素樹脂(II)の結晶に由来するピーク面積)/(全体のピーク面積)
上記全体のピーク面積は、走査角5~40度の範囲で測定した強度を積算したもの(但し、芳香族ポリエーテルケトン樹脂(I)の結晶に由来するピーク面積は除く)である。
フッ素樹脂(II)の結晶に由来するピーク面積は、フッ素樹脂(II)の結晶に由来するピークの面積を合計したものである。
上記芳香族ポリエーテルケトン樹脂(I)の溶融粘度は、ASTM D3835に準拠して測定する。
CF2=CF-Rf1 (1)
(式中、Rf1は、-CF3又は-ORf2を表す。Rf2は、炭素数1~5のパーフルオロアルキル基を表す。)で表される化合物である。
CF2=CF-Rf1 (1)
(式中、Rf1は、-CF3又は-ORf2を表す。Rf2は、炭素数1~5のパーフルオロアルキル基を表す。)で表されるパーフルオロエチレン性不飽和化合物の共重合体であることが更に好ましい。フッ素樹脂(II)としては、1種を用いてもよいし、2種以上を用いてもよい。上記Rf1が、-ORf2である場合、上記Rf2は炭素数が1~3のパーフルオロアルキル基であることが好ましい。
上記フッ素樹脂(II)を用いることによって、優れた機械的強度及び耐磨耗性を有するフィルムを得ることができる。
例えば、非溶融加工性のポリテトラフルオロエチレンを用いた場合には、フィルムの機械的強度が低く、また、充分に低い磨耗特性を有するフィルムを得ることができないおそれがある。
また、上記フッ素樹脂(II)を構成する上記一般式(1)で表されるパーフルオロエチレン性不飽和化合物の含有量の下限は、1モル%がより好ましく、1.5モル%が更に好ましく、4モル%が特に好ましい。上記フッ素樹脂(II)を構成する上記一般式(1)で表されるパーフルオロエチレン性不飽和化合物の含有量の上限は、15モル%がより好ましく、13モル%が更に好ましく、10モル%が特に好ましい。
フッ素樹脂(II)としては、また、テトラフルオロエチレン/ヘキサフルオロプロピレン/単量体α共重合体であって、テトラフルオロエチレン/ヘキサフルオロプロピレン/単量体αのモル比が80~98.5/1.5~20/0~0.9である共重合体も好ましい。フッ素樹脂(II)が上記共重合体であると、芳香族ポリエーテルケトン樹脂(I)中にフッ素樹脂(II)を微小粒子状に分散させることが容易であり、従って、フィルムの成形性、並びに、機械的強度及び耐磨耗性をより一層向上させることができる。上記共重合体は、パーフルオロ(アルキルビニルエーテル)を1モル%以上含むテトラフルオロエチレン/パーフルオロ(アルキルビニルエーテル)共重合体と比べても、これらの効果を奏する点で優れている。単量体αは、テトラフルオロエチレン及びヘキサフルオロプロピレンと共重合可能な単量体である。単量体αとしては、パーフルオロ(アルキルビニルエーテル)が挙げられる。
上記フッ素樹脂(II)の溶融粘度は、ASTM D3835に準拠して測定する。
上記フッ素樹脂(II)のMFRは、ASTM D3307-01に準拠し、メルトインデクサーを用いて測定する。
より優れた機械的強度及び耐磨耗性を有するフィルムを得ることができるとともに、成形性が優れたものとなることから、フッ素樹脂(II)の平均分散粒子径は2.0μm以下であることがより好ましく、1.0μm以下であることが更に好ましく、0.3μm以下であることが特に好ましい。
平均分散粒子径の下限は特に限定されないが0.01μmであってよい。
成形性がより優れたものとなり、機械的強度及び耐磨耗性が向上することから、フッ素樹脂(II)の最大分散粒子径は5μm以下であることがより好ましく、1μm以下であることが更に好ましく、0.5μm以下であることが特に好ましい。
上記のことから、上記樹脂組成物は、芳香族ポリエーテルケトン樹脂(I)及びフッ素樹脂(II)を、L/Dが35以上であるスクリュウ構成の二軸押出機で混合することにより得られるものであることが好ましい。
芳香族ポリエーテルケトン樹脂(I)とフッ素樹脂(II)とを充分に混練することによって、所望の分散状態を有する樹脂組成物を得ることができる。分散状態はフィルムの機械的強度及び耐磨耗性、並びに、成形性に影響を与えるので、樹脂組成物から得られるフィルムにおいて所望の分散状態が得られるように、混練方法の選択は適切に行われるべきである。
上記他の成分は、芳香族ポリエーテルケトン樹脂(I)及びフッ素樹脂(II)に予め添加して混合しておいてもよいし、芳香族ポリエーテルケトン樹脂(I)及びフッ素樹脂(II)を配合するときに添加してもよい。
上記成形工程は、340℃以上の温度で樹脂組成物を成形した後、成形されたフィルムを冷却するものであることが好ましい。上記冷却は、例えば、150℃未満の温度まで行ってよい。
上記のような条件でフィルム成形、場合によっては更に加熱処理を施すことによって、芳香族ポリエーテルケトン樹脂(I)の結晶度が10%以上のフィルムを製造することができる。
本発明者等が、音響特性に優れるスピーカー用振動板について鋭意検討したところ、上記優れた機械的強度及び伸び特性(柔軟性)を有する上記特定の構成を有するフィルムを含むことによって、スピーカー用振動板が優れた音響特性を有しながら、フィルムの機械的強度に起因して優れた機械的強度をも有することを見出し、本発明は完成したものである。
すなわち、本発明は、優れた機械的強度と優れた柔軟性を有し、上記特定の構成を有するフィルムを含むことによって、音響特性特性だけでなく、更に機械的強度にも優れるという未知の属性を発見し、上記フィルムがスピーカー用振動板への使用に特に適することを見いだしたことに基づく発明である。
本発明のスピーカー用振動板は、スピーカーやイヤホン等の振動板(振動膜)として用いられる。
本発明はまた、上記スピーカー用振動板を備えるスピーカー又はイヤホンでもある。
振動の減衰性の観点から、本発明のスピーカー用振動板は、他の基材の片面又は両面に上記フィルムが積層されたものであることが好ましく、他の基材の両面に上記フィルムが積層された3層構造を有するものがより好ましい。
本発明のスピーカー用振動板が上記3層構造を有するものであると、特に周波数特性の安定に優れる。上記3層構造を有するスピーカー用振動板は、スピーカーとしての性能と強度の観点から、他の基材の厚みが5~50μmであり、他の基材の両面に設けられる上記フィルムの厚みが2~20μmであることが好ましい。
上記他の基材としては、一般に振動板の材料として用いられているものが使用でき、例えば、ポリイミド、ポリアミドイミド、ポリエーテルイミド、ポリエチレンナフタレート、ポリエチレンテレフタレート、ウレタン系重合体等からなる基材が挙げられる。
本発明のスラストワッシャーの具体的態様としては、スラストワッシャー形状の成形体の表面に上記フィルムを備えるものが挙げられる。上記スラストワッシャー形状の成形体の材料としては、一般的にスラストワッシャーの材料として用いられているものが使用でき、例えば、ポリオキシメチレン、ポリフェニレンサルファイド、ポリアミド等からなる基材が挙げられる。
結晶化度は、X線回折装置を用い、出力40kV-40mA、走査角5~40度の範囲で広角X線回折を測定し、芳香族ポリエーテルケトン樹脂(1)の結晶に由来するピーク面積及び全体のピーク面積を算出し、下記式により求めた。
結晶化度(%)=100×(芳香族ポリエーテルケトン樹脂(1)の結晶に由来するピーク面積/(全体のピーク面積)
上記全体のピーク面積は、走査角5~40度の範囲で測定した回折強度全回折強度を積算した面積(但し、フッ素樹脂(2)の結晶に由来するピーク面積は除く)である。
芳香族ポリエーテルケトン樹脂(1)の結晶に由来するピーク面積は、芳香族ポリエーテルケトン樹脂(1)の結晶に由来するピークの面積を合計した面積である。
上記フッ素樹脂(2)の結晶に由来するピーク面積は、2θ=17.7度付近に観察されるピークの面積である。
実施例及び比較例で用いたPEEKの結晶に由来するピーク面積は、2θ=18.7度、20.4度、22.3度及び28.6度付近に観察されるピークの面積の合計である。2θ=18.7度付近に観察されるピークは(110)面に由来するピークであり、2θ=20.4度付近に観察されるピークは(111)面に由来するピークであり、2θ=22.3度付近に観察されるピークは(200)面に由来するピークであり、2θ=28.6度付近に観察されるピークは(211)面に由来するピークであると推測される。
実施例及び比較例で得られたフィルムをASTM V型ダンベルを用いて標線間距離7.6mmのダンベル上試験片に打ち抜き、得られたダンベル状試験片を用いて、ASTM D638に準拠して、25℃、チャック間距離24.5mm、引張り速度50mm/minで引張弾性率(MPa)、上降伏点応力(MPa)、引張破断伸び(%)を測定した。結果を表1に示す。
実施例及び比較例で得られたフィルムに対して、リングオンディスク型の摩擦磨耗試験機により、荷重500N/cm2、回転速度0.5m/秒、60分の条件で、S45C(外形20.5mm、内径16.5mm)のリングを用いて摩擦摩耗試験を行い求めた。
実施例及び比較例で得られたフィルムに対して、リングオンディスク型の摩擦磨耗試験機により、荷重50N/cm2、回転速度0.5m/秒、10~15分の条件で、S45C(外形20.5mm、内径16.5mm)のリングを用いて摩擦摩耗試験を行い求めた。
芳香族ポリエーテルケトン樹脂の溶融粘度は、60sec-1、390℃において、ASTM D3835に準拠して測定した。
フッ素樹脂の溶融粘度は、60sec-1、390℃において、ASTM D3835に準拠して測定した。
ASTM D1238に従って、メルトインデクサーを用いて、372℃、5000g荷重下で内径2mm、長さ8mmのノズルから10分間あたりに流出するポリマーの質量(g/10分)を求めた。
実施例及び比較例で得られたフィルムの音質の評価は、JIS C5532に準拠して周波数特性を測定することで行った。
芳香族ポリエーテルケトン樹脂(1):ポリエーテルエーテルケトン(溶融粘度:1.19kNsm-2。)フッ素樹脂(2):テトラフルオロエチレン/ヘキサフルオロプロピレン共重合体(テトラフルオロエチレン/ヘキサフルオロプロピレン/パーフルオロ(プロピロビニルエーテル)=87.5/11.5/1.0(組成重量比)。MFR;23g/10分。融点;260℃、溶融粘度;0.55kNsm-2。
芳香族ポリエーテルケトン樹脂(1)およびフッ素樹脂(2)を表1に示す割合(質量部)で予備混合を行い、二軸押出機を使用して、シリンダー温度390℃、スクリュウ回転数300rpmの条件下で溶融混練し、樹脂組成物を製造した。
得られた樹脂組成物のペレットを、フィルム成形用Tダイ押出機に供給し、シリンダー温度380℃、ダイ温度380℃、スクリュウ回転数7rpmの条件で、かつ表1に示す冷却ロールの温度条件で厚み25μmのフィルムを成形した。この際、押出されたフィルムは冷却ロールに1~10秒接触する。
その後、100℃に設定した冷却ロールで成形したフィルムでは、表1に示すアニール条件にて、結晶化処理を施した。具体的には成形したフィルムを120mmφの金型に挟み、220℃で0.1~3時間、オーブンに入れ、アニールした。
その後、得られたフィルムを用いて、芳香族ポリエーテルケトン樹脂(1)(PEEK)の結晶化度、フィルムの引張弾性率、引張破断伸び、上降伏点応力、摩耗量、動摩擦係数、音響効果を測定した。
取り出したフィルムをオーブンでアニールしなかった点以外は、実施例1と同様にフィルムを作成し、その後得られたフィルムを用いて、PEEKの結晶化度、フィルムの引張弾性率、引張破断伸び、上降伏点応力、摩耗量、動摩擦係数、音響効果を測定した。
Claims (10)
- 芳香族ポリエーテルケトン樹脂(I)及びフッ素樹脂(II)を含むフィルムであって、
芳香族ポリエーテルケトン樹脂(I)の結晶化度が10%以上である
ことを特徴とするフィルム。 - フッ素樹脂(II)は、テトラフルオロエチレン及び下記一般式(1):
CF2=CF-Rf1 (1)
(式中、Rf1は、-CF3又は-ORf2を表す。Rf2は、炭素数1~5のパーフルオロアルキル基を表す。)で表されるパーフルオロエチレン性不飽和化合物の共重合体である請求項1記載のフィルム。 - 芳香族ポリエーテルケトン樹脂(I)とフッ素樹脂(II)との質量比(I):(II)が40:60~99:1である請求項1又は2記載のフィルム。
- フッ素樹脂(II)が芳香族ポリエーテルケトン樹脂(I)中に粒子状に分散している請求項1、2又は3記載のフィルム。
- 芳香族ポリエーテルケトン樹脂(I)中でのフッ素樹脂(II)の平均分散粒子径が、3.0μm以下である請求項4記載のフィルム。
- 芳香族ポリエーテルケトン樹脂(I)とフッ素樹脂(II)との溶融粘度比(I)/(II)が0.01~5.0である請求項1、2、3、4又は5記載のフィルム。
- フッ素樹脂(II)は、メルトフローレートが0.1~100g/10分である請求項1、2、3、4、5又は6記載のフィルム。
- 芳香族ポリエーテルケトン樹脂(I)は、ポリエーテルエーテルケトンである請求項1、2、3、4、5、6又は7記載のフィルム。
- 請求項1、2、3、4、5、6、7又は8記載のフィルムを含むスピーカー用振動板。
- 請求項1、2、3、4、5、6、7又は8記載のフィルムを含むスラストワッシャー。
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JP7336417B2 (ja) | 2020-05-27 | 2023-08-31 | 信越ポリマー株式会社 | スピーカの振動板用樹脂フィルム及びその製造方法、並びにスピーカの振動板 |
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JP6694364B2 (ja) * | 2016-10-14 | 2020-05-13 | 信越ポリマー株式会社 | 振動板用フィルムの製造方法 |
WO2018232119A1 (en) * | 2017-06-15 | 2018-12-20 | Arkema Inc. | Production of semicrystalline parts from pseudo-amorphous polymers |
GB2567468A (en) * | 2017-10-12 | 2019-04-17 | Victrex Mfg Ltd | Polymeric film |
JP7181465B2 (ja) * | 2019-03-27 | 2022-12-01 | ダイキン工業株式会社 | 樹脂組成物および成形品 |
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