US20160177211A1 - Liquid crystalline polyester composition - Google Patents

Liquid crystalline polyester composition Download PDF

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Publication number
US20160177211A1
US20160177211A1 US14/908,345 US201414908345A US2016177211A1 US 20160177211 A1 US20160177211 A1 US 20160177211A1 US 201414908345 A US201414908345 A US 201414908345A US 2016177211 A1 US2016177211 A1 US 2016177211A1
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liquid crystal
crystal polyester
group
polyester composition
mass
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US14/908,345
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Shintaro Komatsu
Mitsuo Maeda
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Sumitomo Chemical Co Ltd
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Sumitomo Chemical Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M107/00Lubricating compositions characterised by the base-material being a macromolecular compound
    • C10M107/20Lubricating compositions characterised by the base-material being a macromolecular compound containing oxygen
    • C10M107/30Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M107/32Condensation polymers of aldehydes or ketones; Polyesters; Polyethers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L67/00Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
    • C08L67/02Polyesters derived from dicarboxylic acids and dihydroxy compounds
    • C08L67/03Polyesters derived from dicarboxylic acids and dihydroxy compounds the dicarboxylic acids and dihydroxy compounds having the carboxyl- and the hydroxy groups directly linked to aromatic rings
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29BPREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B7/00Mixing; Kneading
    • B29B7/002Methods
    • B29B7/007Methods for continuous mixing
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29BPREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B7/00Mixing; Kneading
    • B29B7/30Mixing; Kneading continuous, with mechanical mixing or kneading devices
    • B29B7/58Component parts, details or accessories; Auxiliary operations
    • B29B7/72Measuring, controlling or regulating
    • B29B7/726Measuring properties of mixture, e.g. temperature or density
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29BPREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B7/00Mixing; Kneading
    • B29B7/80Component parts, details or accessories; Auxiliary operations
    • B29B7/88Adding charges, i.e. additives
    • B29B7/90Fillers or reinforcements, e.g. fibres
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29BPREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B9/00Making granules
    • B29B9/12Making granules characterised by structure or composition
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29BPREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
    • B29B9/00Making granules
    • B29B9/12Making granules characterised by structure or composition
    • B29B9/14Making granules characterised by structure or composition fibre-reinforced
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/34Silicon-containing compounds
    • C08K3/36Silica
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K7/00Use of ingredients characterised by shape
    • C08K7/02Fibres or whiskers
    • C08K7/04Fibres or whiskers inorganic
    • C08K7/06Elements
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L27/00Compositions 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
    • C08L27/02Compositions 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
    • C08L27/12Compositions 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
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M125/00Lubricating compositions characterised by the additive being an inorganic material
    • C10M125/02Carbon; Graphite
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M147/00Lubricating compositions characterised by the additive being a macromolecular compound containing halogen
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M169/00Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
    • C10M169/04Mixtures of base-materials and additives
    • C10M169/044Mixtures of base-materials and additives the additives being a mixture of non-macromolecular and macromolecular compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K2201/00Specific properties of additives
    • C08K2201/002Physical properties
    • C08K2201/003Additives being defined by their diameter

Definitions

  • the present invention relates to a liquid, crystal polyester composition containing a liquid crystal polyester and a fluorine resin.
  • a liquid crystal polyester composition containing a liquid crystal polyester and a fluorine resin As the material of a sliding member suitable for use at high temperatures, a liquid crystal polyester composition containing a liquid crystal polyester and a fluorine resin has been studied (see JP-A-63-230756 and JP-A-05-105804). The liquid crystal polyester composition further containing a filler such as a glass fiber and a carbon fiber in the liquid crystal polyester has also been studied (see JP-A-2010-003661).
  • An object of the present invention is to provide a liquid crystal polyester composition that is excellent in slipperiness.
  • the present invention relates to the following inventions.
  • the liquid crystal polyester is a polyester which exhibits liquid crystallinity in a molten state, preferably melts at a temperature of 450° C. or lower.
  • the liquid crystal polyester may be a liquid crystal polyester amide, a liquid crystal polyester ether, a liquid crystal polyester carbonate, or a liquid crystal polyester imide.
  • the liquid crystal polyester is a wholly aromatic liquid crystal polyester, consisting only of an aromatic compound as a raw material monomer.
  • Typical examples of the liquid crystal polyester include: a polymer obtained by polymerizing (polycondensing) an aromatic hydroxy carboxylic acid, an aromatic dicarboxylic acid, and at least one compound selected from the group consisting of an aromatic diol, an aromatic hydroxylamine and an aromatic diamine; a polymer obtained by polymerizing plural kinds of aromatic hydroxy carboxylic acid; a polymer obtained by polymerizing an aromatic dicarboxylic acid and at least one compound selected from the group consisting of an aromatic diol, an aromatic hydroxylamine and an aromatic diamine; and a polymer obtained by polymerizing a polyester, such as polyethylene terephthalate, and an aromatic hydroxy carboxylic acid.
  • Polymerizable derivatives of the aromatic hydroxy carboxylic acid, aromatic dicarboxylic acid, aromatic diol, aromatic hydroxylamine, and aromatic diamine may also be used for the polymerization described above.
  • Examples of the polymerizable derivatives of carboxyl group-containing compounds include an ester obtained by converting a carboxyl group into an alkoxycarbonyl group or an aryloxycarbonyl group, an acid halide obtained by converting a carboxyl group into a haloformyl group, and an acid anhydride obtained by converting a carboxyl group into an acyloxycarbonyl group.
  • Examples of the polymerizable derivatives of hydroxyl group-containing compounds such as an aromatic hydroxy carboxylic acid, an aromatic diol, and an aromatic hydroxylamine, include an acylated derivative obtained by acylating a hydroxyl group to convert it into an acyloxyl group.
  • Examples of the polymerizable derivatives of amino group-containing compounds, such as an aromatic hydroxylamine and an aromatic diamine include an acylated derivative obtained by acylating an amino group to convert it into an acylamino group.
  • the liquid crystal polyester preferably has a repeating unit represented by the following formula (1) (hereinafter also referred to as “repeating unit (1)”), and more preferably has the repeating unit (1), a repeating unit represented by the following formula (2) (hereinafter also referred to as “repeating unit (2)”), and a repeating unit represented by the following formula (3) (hereinafter also referred to as “repeating unit (3)”).
  • halogen atom examples include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom.
  • alkyl group examples include a methyl group, an ethyl group, a n-propyl group, an isopropyl group, a n-butyl group, an isobutyl group, a s-butyl group, a t-butyl group, a n-hexyl group, a 2-ethylhexyl group, a n-octyl group and a n-decyl group, each of which usually has 1 to 10 carbon atoms.
  • aryl group examples include a phenyl group, an o-tolyl group, a m-tolyl group, a p-tolyl group, a 1-naphthyl group and a 2-naphthyl group, and the carbon number thereof is usually 6 to 20.
  • the number of the substituted group is usually 2 or less, and preferably 1 or less.
  • alkylidene group examples include a methylene group, an ethylidene group, an isopropylidene group, a n-butylidene group and a 2-ethylhexylidene group, and the carbon number thereof is usually 1 to 10.
  • the repeating unit (1) is a repeating unit derived from a given aromatic hydroxy carboxylic acid.
  • the repeating unit (1) is preferably a repeating unit in which Ar 1 is a p-phenylene group (a repeating unit derived from p-hydroxybenzoic acid), or a repeating unit in which Ar 1 is a 2,6-naphthylene group (a repeating unit derived from 6-hydroxy-2-naphthoic acid).
  • the repeating unit (2) is a repeating unit derived from a given aromatic dicarboxylic acid.
  • the repeating unit (2) is preferably a repeating unit in which Ar 2 is a p-phenylene group (a repeating unit derived from terephthalic acid); Ar 2 is a m-phenylene group (a repeating unit derived from isophthalic acid); or Ar 2 is a 2,6-naphthylene group (a repeating unit derived from 2,6-naphthalenedicarboxylic acid).
  • the repeating unit (3) is a repeating unit derived from a given aromatic diol, aromatic hydroxylamine or aromatic diamine.
  • the repeating unit (3) is preferably a repeating unit in which Ar 3 is a p-phenylene group (a repeating unit derived from hydroquinone, p-aminophenol or p-phenylenediamine), or Ar 3 is a 4,4′-biphenylylene group (a repeating unit derived from 4,4′-dihydroxybiphenyl, 4-amino-4′-hydroxybiphenyl or 4,4′-diaminobiphenyl).
  • the amount of the repeating unit (1) contained is usually 30 mol % or more, preferably 30 to 80 mol %, more preferably 40 to 70 mol %, and further preferably 45 to 65 mol %, relative to the total amount of all repeating units.
  • the amount of the repeating unit (2) contained is usually 35 mol % or less, preferably 10 to 35 mol %, more preferably 15 to 30 mol %, and further preferably 17.5 to 27.5 mol %, relative to the total amount of all repeating units.
  • the amount of the repeating unit (3) contained is usually 35 mol % or less, preferably 10 to 35 mol %, more preferably 15 to 30 mol %, and further preferably 17.5 to 27.5 mol %, relative to the total amount of all repeating units.
  • total amount of all repeating units refers to a value obtained by dividing mass of each of the repeating units constituting the liquid crystal polyester by formula weight of each of the repeating units to calculate each amount of substance (moles) of the respective repeating units, and then summing each amount of substance obtained.
  • the melt temperature and melt viscosity can be adjusted to an appropriate range, thus the molding temperature can be set not too high.
  • the amount ratio of the repeating unit (2) to the repeating unit (3) is usually 0.9/1 to 1/0.9, preferably 0.95/1 to 1/0.95, and more preferably 0.98/1 to 1/0.98.
  • the repeating units (1) to (3) in the liquid crystal polyester may each independently have two or more kinds or more.
  • the liquid crystal polyester may have a repeating unit other than the repeating units (1) to (3), provided that the amount thereof is usually 10 mol % or less, and preferably 5 mol % or less, relative to the total amount of all repeating units.
  • the liquid crystal polyester preferably has a repeating unit such that X and Y are each an oxygen atom, that is, a repeating unit derived from a given aromatic diol, as the repeating unit (3), because it facilitates reduction in melt viscosity, and more preferably has exclusively a repeating unit such that X and Y are each an oxygen atom, as the repeating unit (3).
  • the liquid crystal polyester is produced by melt-polymerizing raw material monomers corresponding to the respective repeating units constituting the liquid crystal polyester to obtain a polymer (hereinafter may be referred to as “prepolymer”), followed by subjecting the obtained prepolymer to solid phase polymerization.
  • prepolymer a polymer
  • the melt polymerization may be carried out in the presence of a catalyst
  • the catalyst include metal compounds such as magnesium acetate, stannous acetate, tetrabutyl titanate, lead acetate, sodium acetate, potassium acetate and antimony trioxide, and nitrogen-containing heterocyclic compounds such as 4-(dimethylamino)pyridine and 1-methylimidazole. Among them, nitrogen-containing heterocyclic compounds are preferred.
  • the liquid crystal polyester usually has an incipient fluidization temperature of 270° C. or more, preferably 270 to 400° C., and more preferably 280 to 380° C.
  • the melt temperature and melt viscosity can be adjusted to an appropriate range, thus the molding temperature can be set not too high.
  • the incipient fluidization temperature also called flow temperature or fluidizing temperature, is a temperature at which the viscosity reaches 4800 Pa ⁇ s (48000 poises) as measured by melting the liquid crystal polyester while heating it at a rate of 4° C./min, and extruding the melt under a load of 9.8 MPa (100 kg/cm 2 ) through a nozzle with an inner diameter of 1 mm and a length of 10 mm, using a capillary rheometer.
  • the incipient fluidization temperature gives an indication of a molecular weight of a liquid crystal polyester (see “Liquid Crystal Polymers—Synthesis, Molding, and Applications—”, edited by Naoyuki Koide, CMC Publishing Co., Ltd., Jun. 5, 1987, p 95).
  • fluorine resin examples include polytetrafluoroethylene (PTFE), a tetrafluoroethylene-hexafluoropropylene copolymer, polytrichlorofluoroethylene, and a tetrafluoroethylene-perfluoroalkylvinylether copolymer.
  • PTFE polytetrafluoroethylene
  • the composition of the present invention may contain two or more kinds of fluorine resins.
  • the content of the fluorine resin in the liquid crystal polyester composition is usually 5 to 30 parts by mass, and preferably 5 to 20 parts by mass, relative to 100 parts by mass of the liquid crystal polyester.
  • the melt flowability and strength/rigidity of the liquid crystal polyester composition can be adjusted to an appropriate range.
  • the carbon fiber may be a PAN-based carbon fiber using polyacrylonitrile as a raw material, a pitch-based carbon fiber using coal tar or petroleum pitch as a raw material, a cellulosic carbon fiber using viscose rayon, a cellulose acetate or the like as a raw material, or a vapor growing carbon fiber using hydrocarbon or the like as a raw material, and two or more kinds of them may be used.
  • the carbon fiber may be a chopped carbon fiber or a milled carbon fiber, and two or more kinds of them may be used.
  • the number average fiber diameter of the carbon fiber is usually 5 to 20 ⁇ m, and preferably 5 to 15 ⁇ m, and the number average aspect ratio (number average fiber length/number average fiber diameter) of the carbon fiber is usually 10 to 200, and preferably 20 to 100.
  • the number average fiber diameter and number average fiber length of the carbon fiber can be measured by electron microscope observation.
  • the carbon fiber usually breaks when mixing with the liquid crystal polyester by melt kneading or the like. Therefore, for example, using a long carbon fiber having a number average aspect ratio of 500 or more as a raw material, this carbon fiber may be allowed to break when mixing it, so that the aspect ratio thereof is within the above range.
  • the content of the carbon fiber in the liquid crystal polyester composition is usually 10 to 40 parts by mass, and preferably 15 to 30 parts by mass, relative to 100 parts by mass of the liquid crystal polyester.
  • the higher the content of the carbon fiber the stronger the tendency to have improved wear resistance and strength/rigidity of the liquid crystal polyester composition.
  • wear of the mating material slid to each other can be suppressed.
  • the granular filler is a filler having a shape other than fibrous and plate-like shape, and is a filler having a spherical or other shape.
  • a granular inorganic filler is preferable, and other preferable examples include aluminum oxide, silicon oxide and titanium oxide, and two kinds or more of them may be used.
  • the volume average particle diameter of the granular filler is usually 20 ⁇ m or less, preferably 5 ⁇ m or less, and more preferably 1 ⁇ m or less, from the viewpoint of slipperiness of the liquid crystal polyester composition, wear resistance of the liquid crystal polyester composition, and difficulty of wearing of the mating material slid to each other.
  • the volume average particle diameter of the granular filler is usually 0.1 ⁇ m or more.
  • the volume average particle diameter of the granular filler can be measured by a laser diffraction method.
  • the appropriate amount of the granular filler is put into a solvent (aqueous sodium hexametaphosphate solution, etc.), and the granular filler is dispersed in the solvent for 10 minutes with an ultrasonic cleaning machine or the like, then irradiated with a laser beam, and the volume average particle diameter of the granular filler can be obtained from transmission diffraction.
  • a solvent aqueous sodium hexametaphosphate solution, etc.
  • These operations can be performed by using Microtrac particle size analyzer such as MT-3000 II (NIKKISO CO., LTD.).
  • the number average aspect ratio of the granular filler (number average maximum diameter/number average minimum diameter) is usually 1 to 2, and preferably 1 to 1.5, and it is preferred that the number average aspect ratio is approximately 1, namely, the granular filler is nearly spherical.
  • the content of the granular filler in the liquid crystal polyester composition is usually 5 to 30 parts by mass, preferably 5 to 20 parts by mass, and more preferably 5 to 15 parts by mass, relative to 100 parts by mass of the liquid crystal polyester.
  • liquid crystal polyester composition further contains a plate-like filler, from the viewpoint of slipperiness.
  • a plate-like inorganic filler is preferred, and preferable examples thereof include mica and graphite, and two or more kinds of them may be used.
  • the volume average particle diameter of the plate-like filler is usually 1 to 80 ⁇ m or less, and preferably 3 to 50 ⁇ m or less.
  • the volume average particle diameter of the plate-like filler can be measured by a laser diffraction method. For example, the appropriate amount of the plate-like filler is put into a solvent such as ethanol, and the plate-like filler is dispersed in the solvent for 10 minutes with an ultrasonic cleaning machine or the like, then irradiated with a laser beam.
  • the area of the projected image of the plate-like filler from the visual field direction is obtained, and the diameter of the circle assuming the same circle having the same area (area circle equivalent diameter) is read as the particle diameter of the plate-like filler, and the arithmetic average value is calculated, whereby the volume average particle diameter of the plate-like filler can be obtained.
  • These operations can be performed by using Microtrac particle size analyzer such as MT-3000 II (NIKKISO CO., LTD.).
  • the number average aspect ratio of the plate-like filler (number average plate surface diameter (area circle equivalent diameter)/number average plate thickness) is usually 5 to 200, and preferably 10 to 100.
  • the number average plate surface diameter and number average plate thickness of the plate-like filler can be measured by electron microscope observation.
  • the content of the plate-like filler in the liquid crystal polyester composition is usually 5 to 20 parts by mass, and preferably 5 to 10 parts by mass, relative to 100 parts by mass of the liquid crystal polyester.
  • the liquid crystal polyester composition may contain other component as necessary, for example, a resin other than a liquid crystal polyester and a fluorine resin, a fibrous filler other than a carbon fiber, additives such as an antioxidant, a thermal stabilizer, an ultraviolet absorber, an antistatic agent, a surfactant, a flame retardant and coloring agent.
  • a resin other than a liquid crystal polyester and a fluorine resin for example, a resin other than a liquid crystal polyester and a fluorine resin, a fibrous filler other than a carbon fiber, additives such as an antioxidant, a thermal stabilizer, an ultraviolet absorber, an antistatic agent, a surfactant, a flame retardant and coloring agent.
  • additives such as an antioxidant, a thermal stabilizer, an ultraviolet absorber, an antistatic agent, a surfactant, a flame retardant and coloring agent.
  • the content of the other component, or the total content when a plurality of other components is contained is usually 10 parts by mass or less, relative to 100 parts by mass of
  • the liquid crystal polyester composition is preferably prepared by melt-kneading a liquid crystal polyester, a fluorine resin, a carbon fiber, a granular filler, and a plate-like filler and other components used as necessary, using an extruder, extruding it in a strand shape, and pelletizing it.
  • the extruder used is preferably an extruder including a cylinder, one or more screws provided in the cylinder and one or more feed ports provided on the cylinder, more preferably such an extruder further including one or more vent parts provided in the cylinder.
  • the liquid crystal polyester composition of the present invention is excellent in slipperiness, thus preferably used in the material of a sliding member.
  • the sliding member include bearing, slider, gear, cam and seal ring.
  • Molding of the liquid crystal polyester composition into a sliding member is preferably performed by melt molding, and more preferably performed by injection molding.
  • the mixture was heated by raising the temperature from room temperature to 145° C. over 15 minutes under stirring, followed by reflux at 145° C. for 1 hour. Subsequently, the temperature was raised from 145° C. to 310° C. over 3 hours and 30 minutes while distilling off by-product acetic acid and unreacted acetic anhydride, and maintained at 310° C. for 3 hours, then the content of the reactor was taken out, and cooled to room temperature.
  • the obtained solid was pulverized to a particle size of about 0.1 to 1 mm by a pulverizer, then, in a nitrogen atmosphere, the pulverized material was heated by raising the temperature from room temperature to 250° C. over 1 hour, then further raising it from 250° C. to 310° C. over 10 hours, and maintained at 310° C. for 5 hours to carry out solid phase polymerization of the material. After solid phase polymerization, the resultant was cooled to afford powdery liquid crystal polyester.
  • This liquid crystal polyester was found to have 55 mol % of a repeating unit (1) in which Ar 1 is a 2,6-naphthylene group, 17.5 mol % of a repeating unit (2) in which Ar 2 is a 2,6-naphthylene group, 5 mol % of a repeating unit (2) in which Ar 2 is a 1,4-phenylene group, and 22.5% of a repeating unit (3) in which Ar 3 is a 1,4-phenylene group, and X and Y are each oxygen atom, and have an incipient fluidization temperature of 333° C.
  • polytetrafluoroethylene (“Dyneon TF9205” of Sumitomo 3M) was used.
  • a chopped carbon fiber with a number-average fiber diameter of 7 ⁇ m and a number-average fiber length of 6 mm (“TR06UB4E” of MITSUBISHI RAYON CO., LTD.) was used.
  • Plate-like filler (1) Mica with a volume average particle diameter of 24 ⁇ m (“AB25S” of YAMAGUCHI MICA CO., LTD.)
  • Plate-like filler (2) Graphite with a volume average particle diameter of 5 ⁇ m (“J-CPB” of Nippon Graphite Industories, ltd.)
  • Plate-like filler (3) Graphite with a volume average particle diameter of 19 ⁇ m (“CPB” of Nippon Graphite Industories, ltd.)
  • a liquid crystal polyester, a fluorine resin, a carbon fiber, a granular filler and a plate-like filler were melt-kneaded at 320° C. in a ratio shown in Table 1, and pelletized, using a co-rotating twin-screw extruder (“PCM-30HS” of Ikegai Corp).
  • the obtained pellet was injection molded at a cylinder nozzle temperature of 320° C., a mold temperature of 130° C., and an injection speed of 530 cm 3 /s, to obtain a molded body having a length of 126 mm, a width of 12.5 mm, and a thickness of 3.2 mm.
  • the liquid crystal polyester composition of the present invention is excellent in slipperiness, thus is useful as a material of a sliding member.

Abstract

A liquid crystal polyester composition contains a liquid crystal polyester, a fluorine resin, a carbon fiber, and a granular filler.

Description

    TECHNICAL FIELD
  • The present invention relates to a liquid, crystal polyester composition containing a liquid crystal polyester and a fluorine resin.
  • BACKGROUND ART
  • As the material of a sliding member suitable for use at high temperatures, a liquid crystal polyester composition containing a liquid crystal polyester and a fluorine resin has been studied (see JP-A-63-230756 and JP-A-05-105804). The liquid crystal polyester composition further containing a filler such as a glass fiber and a carbon fiber in the liquid crystal polyester has also been studied (see JP-A-2010-003661).
  • DISCLOSURE OF THE INVENTION
  • An object of the present invention is to provide a liquid crystal polyester composition that is excellent in slipperiness. The present invention relates to the following inventions.
      • [1] A liquid crystal polyester composition containing a liquid crystal polyester, a fluorine resin, a carbon fiber, and a granular filler.
      • [2] The liquid crystal polyester composition according to the item [1], wherein the liquid crystal polyester is a liquid crystal polyester having a repeating unit represented by formula (1), a repeating unit represented by formula (2), and a repeating unit represented by formula (3).
      • (1) —O—Ar1—CO—
      • (2) —CO—Ar2—CO—
      • (3) —X—Ar3—Y—
        wherein Ar1 represents a phenylene group, a naphthylene group, or a biphenylylene group; Ar2 and Ar3 each independently represent a phenylene group, a naphthylene group, a biphenylylene group, or a group represented by formula (4); X and Y each independently represent an oxygen atom or an imino group; and each hydrogen atom present in the group represented by Ar1, Ar2 or Ar3 may be independently substituted with a halogen atom, an alkyl group or an aryl group;
      • (4) —Ar4—Z—Ar5
        wherein Ar4 and Ar5 each independently represent a phenylene group or a naphthylene group; and Z represents an oxygen atom, a sulfur atom, a carbonyl group, a sulfonyl group or an alkylidene group.
      • [3] The liquid crystal polyester composition according to the item [2], wherein the liquid crystal polyester is a liquid crystal polyester having 30 to 80 mol % of the repeating unit represented by formula (1), 10 to 35 mol % of the repeating unit represented by formula (2), and 10 to 35 mol % of the repeating unit represented by formula (3), relative to the total amount of all repeating units of the liquid crystal polyester.
      • [4] The liquid crystal polyester composition according to any one of the items [1] to [3], wherein the granular filler is at least one granular filler selected from the group consisting of aluminum oxide, silicon oxide and titanium oxide.
      • [5] The liquid crystal polyester composition according to any one of the items [1] to [4], wherein the volume average particle diameter of the granular filler is 1 μm or less.
      • [6] The liquid crystal polyester composition according to any one of the items [1] to [5], wherein the content of the fluorine resin is 5 to 20 parts by mass, relative to 100 parts by mass of the liquid crystal polyester.
      • [7] The liquid crystal polyester composition according to any one of the items [1] to [6], wherein the content of the carbon fiber is 15 to 30 parts by mass, relative to 100 parts by mass of the liquid crystal polyester.
      • [8] The liquid crystal polyester composition according to any one of the items [1] to [7], wherein the content of the granular filler is 5 to 20 parts by mass, relative to 100 parts by mass of the liquid crystal polyester.
      • [9] The liquid crystal polyester composition according to any one of the items [1] to [8], further containing a plate-like filler.
      • [10] The liquid crystal polyester composition according to the item [9], wherein the plate-like filler is at least one of plate-like fillers selected from the group consisting of mica and graphite.
      • [11] The liquid crystal polyester composition according to the item [9] or [10], wherein the content of the plate-like filler is 5 to 10 parts by mass, relative to 100 parts by mass of the liquid crystal polyester.
      • [12] A sliding member obtained by molding the liquid crystal polyester composition as defined in any one of the items [1] to [11].
    MODE FOR CARRYING OUT THE INVENTION
  • The liquid crystal polyester is a polyester which exhibits liquid crystallinity in a molten state, preferably melts at a temperature of 450° C. or lower. The liquid crystal polyester may be a liquid crystal polyester amide, a liquid crystal polyester ether, a liquid crystal polyester carbonate, or a liquid crystal polyester imide. Preferably, the liquid crystal polyester is a wholly aromatic liquid crystal polyester, consisting only of an aromatic compound as a raw material monomer.
  • Typical examples of the liquid crystal polyester include: a polymer obtained by polymerizing (polycondensing) an aromatic hydroxy carboxylic acid, an aromatic dicarboxylic acid, and at least one compound selected from the group consisting of an aromatic diol, an aromatic hydroxylamine and an aromatic diamine; a polymer obtained by polymerizing plural kinds of aromatic hydroxy carboxylic acid; a polymer obtained by polymerizing an aromatic dicarboxylic acid and at least one compound selected from the group consisting of an aromatic diol, an aromatic hydroxylamine and an aromatic diamine; and a polymer obtained by polymerizing a polyester, such as polyethylene terephthalate, and an aromatic hydroxy carboxylic acid. Polymerizable derivatives of the aromatic hydroxy carboxylic acid, aromatic dicarboxylic acid, aromatic diol, aromatic hydroxylamine, and aromatic diamine may also be used for the polymerization described above.
  • Examples of the polymerizable derivatives of carboxyl group-containing compounds, such as an aromatic hydroxy carboxylic acid and an aromatic dicarboxylic acid, include an ester obtained by converting a carboxyl group into an alkoxycarbonyl group or an aryloxycarbonyl group, an acid halide obtained by converting a carboxyl group into a haloformyl group, and an acid anhydride obtained by converting a carboxyl group into an acyloxycarbonyl group. Examples of the polymerizable derivatives of hydroxyl group-containing compounds, such as an aromatic hydroxy carboxylic acid, an aromatic diol, and an aromatic hydroxylamine, include an acylated derivative obtained by acylating a hydroxyl group to convert it into an acyloxyl group. Examples of the polymerizable derivatives of amino group-containing compounds, such as an aromatic hydroxylamine and an aromatic diamine, include an acylated derivative obtained by acylating an amino group to convert it into an acylamino group.
  • The liquid crystal polyester preferably has a repeating unit represented by the following formula (1) (hereinafter also referred to as “repeating unit (1)”), and more preferably has the repeating unit (1), a repeating unit represented by the following formula (2) (hereinafter also referred to as “repeating unit (2)”), and a repeating unit represented by the following formula (3) (hereinafter also referred to as “repeating unit (3)”).
      • (1) —O—Ar1—CO—
      • (2) —CO—Ar2—CO—
      • (3) —X—Ar3—Y—
        wherein Ar1 represents a phenylene group, a naphthylene group, or a biphenylylene group; Ar2 and Ar3 each independently represent a phenylene group, a naphthylene group, a biphenylylene group, or a group represented by the following formula (4); X and Y each independently represent an oxygen atom or an imino group (—NH—); and each hydrogen atom present in the group represented by Ar1, Ar2 or Ar3 may be independently substituted with a halogen atom, an alkyl group or an aryl group.
      • (4) —Ar4—Z—Ar5
        wherein Ar4 and Ar5 each independently represent a phenylene group or a naphthylene group; and Z represents an oxygen atom, a sulfur atom, a carbonyl group, a sulfonyl group or an alkylidene group.
  • Examples of the halogen atom include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom. Examples of the alkyl group include a methyl group, an ethyl group, a n-propyl group, an isopropyl group, a n-butyl group, an isobutyl group, a s-butyl group, a t-butyl group, a n-hexyl group, a 2-ethylhexyl group, a n-octyl group and a n-decyl group, each of which usually has 1 to 10 carbon atoms. Examples of the aryl group include a phenyl group, an o-tolyl group, a m-tolyl group, a p-tolyl group, a 1-naphthyl group and a 2-naphthyl group, and the carbon number thereof is usually 6 to 20.
  • In the case where the hydrogen atom is substituted in each of the groups represented by Ar1, Ar2 or Ar3, the number of the substituted group is usually 2 or less, and preferably 1 or less.
  • Examples of the alkylidene group include a methylene group, an ethylidene group, an isopropylidene group, a n-butylidene group and a 2-ethylhexylidene group, and the carbon number thereof is usually 1 to 10.
  • The repeating unit (1) is a repeating unit derived from a given aromatic hydroxy carboxylic acid. The repeating unit (1) is preferably a repeating unit in which Ar1 is a p-phenylene group (a repeating unit derived from p-hydroxybenzoic acid), or a repeating unit in which Ar1 is a 2,6-naphthylene group (a repeating unit derived from 6-hydroxy-2-naphthoic acid).
  • The repeating unit (2) is a repeating unit derived from a given aromatic dicarboxylic acid. The repeating unit (2) is preferably a repeating unit in which Ar2 is a p-phenylene group (a repeating unit derived from terephthalic acid); Ar2 is a m-phenylene group (a repeating unit derived from isophthalic acid); or Ar2 is a 2,6-naphthylene group (a repeating unit derived from 2,6-naphthalenedicarboxylic acid).
  • The repeating unit (3) is a repeating unit derived from a given aromatic diol, aromatic hydroxylamine or aromatic diamine. The repeating unit (3) is preferably a repeating unit in which Ar3 is a p-phenylene group (a repeating unit derived from hydroquinone, p-aminophenol or p-phenylenediamine), or Ar3 is a 4,4′-biphenylylene group (a repeating unit derived from 4,4′-dihydroxybiphenyl, 4-amino-4′-hydroxybiphenyl or 4,4′-diaminobiphenyl).
  • The amount of the repeating unit (1) contained is usually 30 mol % or more, preferably 30 to 80 mol %, more preferably 40 to 70 mol %, and further preferably 45 to 65 mol %, relative to the total amount of all repeating units. The amount of the repeating unit (2) contained is usually 35 mol % or less, preferably 10 to 35 mol %, more preferably 15 to 30 mol %, and further preferably 17.5 to 27.5 mol %, relative to the total amount of all repeating units. The amount of the repeating unit (3) contained is usually 35 mol % or less, preferably 10 to 35 mol %, more preferably 15 to 30 mol %, and further preferably 17.5 to 27.5 mol %, relative to the total amount of all repeating units.
  • The “total amount of all repeating units” herein refers to a value obtained by dividing mass of each of the repeating units constituting the liquid crystal polyester by formula weight of each of the repeating units to calculate each amount of substance (moles) of the respective repeating units, and then summing each amount of substance obtained.
  • The larger the amount of the repeating unit (1) is, the stronger the tendency to have improved melt flowability, heat resistance, and strength/rigidity. When the amount is within the normal range described above, the melt temperature and melt viscosity can be adjusted to an appropriate range, thus the molding temperature can be set not too high.
  • The amount ratio of the repeating unit (2) to the repeating unit (3), represented by {amount of repeating unit (2)}/{amount of repeating unit (3)} (mol/mol), is usually 0.9/1 to 1/0.9, preferably 0.95/1 to 1/0.95, and more preferably 0.98/1 to 1/0.98.
  • The repeating units (1) to (3) in the liquid crystal polyester may each independently have two or more kinds or more. The liquid crystal polyester may have a repeating unit other than the repeating units (1) to (3), provided that the amount thereof is usually 10 mol % or less, and preferably 5 mol % or less, relative to the total amount of all repeating units.
  • The liquid crystal polyester preferably has a repeating unit such that X and Y are each an oxygen atom, that is, a repeating unit derived from a given aromatic diol, as the repeating unit (3), because it facilitates reduction in melt viscosity, and more preferably has exclusively a repeating unit such that X and Y are each an oxygen atom, as the repeating unit (3).
  • It is preferred that the liquid crystal polyester is produced by melt-polymerizing raw material monomers corresponding to the respective repeating units constituting the liquid crystal polyester to obtain a polymer (hereinafter may be referred to as “prepolymer”), followed by subjecting the obtained prepolymer to solid phase polymerization. This makes it possible to produce the liquid crystal polyester with high molecular weight having enhanced heat resistance and strength/rigidity in a manner of good handleability. The melt polymerization may be carried out in the presence of a catalyst, and examples of the catalyst include metal compounds such as magnesium acetate, stannous acetate, tetrabutyl titanate, lead acetate, sodium acetate, potassium acetate and antimony trioxide, and nitrogen-containing heterocyclic compounds such as 4-(dimethylamino)pyridine and 1-methylimidazole. Among them, nitrogen-containing heterocyclic compounds are preferred.
  • The liquid crystal polyester usually has an incipient fluidization temperature of 270° C. or more, preferably 270 to 400° C., and more preferably 280 to 380° C. The higher the incipient fluidization temperature is, the stronger the tendency of the polyester to have improved heat resistance and strength/rigidity. When the incipient fluidization temperature is within normal range described above, the melt temperature and melt viscosity can be adjusted to an appropriate range, thus the molding temperature can be set not too high.
  • The incipient fluidization temperature, also called flow temperature or fluidizing temperature, is a temperature at which the viscosity reaches 4800 Pa·s (48000 poises) as measured by melting the liquid crystal polyester while heating it at a rate of 4° C./min, and extruding the melt under a load of 9.8 MPa (100 kg/cm2) through a nozzle with an inner diameter of 1 mm and a length of 10 mm, using a capillary rheometer. The incipient fluidization temperature gives an indication of a molecular weight of a liquid crystal polyester (see “Liquid Crystal Polymers—Synthesis, Molding, and Applications—”, edited by Naoyuki Koide, CMC Publishing Co., Ltd., Jun. 5, 1987, p 95).
  • Examples of the fluorine resin include polytetrafluoroethylene (PTFE), a tetrafluoroethylene-hexafluoropropylene copolymer, polytrichlorofluoroethylene, and a tetrafluoroethylene-perfluoroalkylvinylether copolymer. The composition of the present invention may contain two or more kinds of fluorine resins.
  • The content of the fluorine resin in the liquid crystal polyester composition is usually 5 to 30 parts by mass, and preferably 5 to 20 parts by mass, relative to 100 parts by mass of the liquid crystal polyester. The higher the content of the fluorine resin, the stronger the tendency to have improved slipperiness of the liquid crystal polyester composition. When the content is within the normal range described above, the melt flowability and strength/rigidity of the liquid crystal polyester composition can be adjusted to an appropriate range.
  • The carbon fiber may be a PAN-based carbon fiber using polyacrylonitrile as a raw material, a pitch-based carbon fiber using coal tar or petroleum pitch as a raw material, a cellulosic carbon fiber using viscose rayon, a cellulose acetate or the like as a raw material, or a vapor growing carbon fiber using hydrocarbon or the like as a raw material, and two or more kinds of them may be used. Also, the carbon fiber may be a chopped carbon fiber or a milled carbon fiber, and two or more kinds of them may be used.
  • The number average fiber diameter of the carbon fiber is usually 5 to 20 μm, and preferably 5 to 15 μm, and the number average aspect ratio (number average fiber length/number average fiber diameter) of the carbon fiber is usually 10 to 200, and preferably 20 to 100. The number average fiber diameter and number average fiber length of the carbon fiber can be measured by electron microscope observation.
  • The carbon fiber usually breaks when mixing with the liquid crystal polyester by melt kneading or the like. Therefore, for example, using a long carbon fiber having a number average aspect ratio of 500 or more as a raw material, this carbon fiber may be allowed to break when mixing it, so that the aspect ratio thereof is within the above range.
  • The content of the carbon fiber in the liquid crystal polyester composition is usually 10 to 40 parts by mass, and preferably 15 to 30 parts by mass, relative to 100 parts by mass of the liquid crystal polyester. The higher the content of the carbon fiber, the stronger the tendency to have improved wear resistance and strength/rigidity of the liquid crystal polyester composition. When the content is within the normal range described above, wear of the mating material slid to each other can be suppressed.
  • The granular filler is a filler having a shape other than fibrous and plate-like shape, and is a filler having a spherical or other shape. As the granular filler, a granular inorganic filler is preferable, and other preferable examples include aluminum oxide, silicon oxide and titanium oxide, and two kinds or more of them may be used.
  • The volume average particle diameter of the granular filler is usually 20 μm or less, preferably 5 μm or less, and more preferably 1 μm or less, from the viewpoint of slipperiness of the liquid crystal polyester composition, wear resistance of the liquid crystal polyester composition, and difficulty of wearing of the mating material slid to each other. The volume average particle diameter of the granular filler is usually 0.1 μm or more.
  • The volume average particle diameter of the granular filler can be measured by a laser diffraction method. For example, the appropriate amount of the granular filler is put into a solvent (aqueous sodium hexametaphosphate solution, etc.), and the granular filler is dispersed in the solvent for 10 minutes with an ultrasonic cleaning machine or the like, then irradiated with a laser beam, and the volume average particle diameter of the granular filler can be obtained from transmission diffraction. These operations can be performed by using Microtrac particle size analyzer such as MT-3000 II (NIKKISO CO., LTD.).
  • The number average aspect ratio of the granular filler (number average maximum diameter/number average minimum diameter) is usually 1 to 2, and preferably 1 to 1.5, and it is preferred that the number average aspect ratio is approximately 1, namely, the granular filler is nearly spherical.
  • The content of the granular filler in the liquid crystal polyester composition is usually 5 to 30 parts by mass, preferably 5 to 20 parts by mass, and more preferably 5 to 15 parts by mass, relative to 100 parts by mass of the liquid crystal polyester. The higher the content of the granular filler, the stronger the tendency to have improved slipperiness of the liquid crystal polyester composition.
  • When the content is within the normal range described above, a composition with good wear resistance can be obtained.
  • It is preferred that the liquid crystal polyester composition further contains a plate-like filler, from the viewpoint of slipperiness.
  • As the plate-like filler, a plate-like inorganic filler is preferred, and preferable examples thereof include mica and graphite, and two or more kinds of them may be used.
  • The volume average particle diameter of the plate-like filler is usually 1 to 80 μm or less, and preferably 3 to 50 μm or less. The volume average particle diameter of the plate-like filler can be measured by a laser diffraction method. For example, the appropriate amount of the plate-like filler is put into a solvent such as ethanol, and the plate-like filler is dispersed in the solvent for 10 minutes with an ultrasonic cleaning machine or the like, then irradiated with a laser beam. The area of the projected image of the plate-like filler from the visual field direction is obtained, and the diameter of the circle assuming the same circle having the same area (area circle equivalent diameter) is read as the particle diameter of the plate-like filler, and the arithmetic average value is calculated, whereby the volume average particle diameter of the plate-like filler can be obtained. These operations can be performed by using Microtrac particle size analyzer such as MT-3000 II (NIKKISO CO., LTD.).
  • The number average aspect ratio of the plate-like filler (number average plate surface diameter (area circle equivalent diameter)/number average plate thickness) is usually 5 to 200, and preferably 10 to 100.
  • The number average plate surface diameter and number average plate thickness of the plate-like filler can be measured by electron microscope observation.
  • The content of the plate-like filler in the liquid crystal polyester composition is usually 5 to 20 parts by mass, and preferably 5 to 10 parts by mass, relative to 100 parts by mass of the liquid crystal polyester.
  • When the content of the plate-like filler is within the normal range described above, wear resistance of the liquid crystal polyester composition can be improved.
  • The liquid crystal polyester composition may contain other component as necessary, for example, a resin other than a liquid crystal polyester and a fluorine resin, a fibrous filler other than a carbon fiber, additives such as an antioxidant, a thermal stabilizer, an ultraviolet absorber, an antistatic agent, a surfactant, a flame retardant and coloring agent. The content of the other component, or the total content when a plurality of other components is contained, is usually 10 parts by mass or less, relative to 100 parts by mass of the liquid crystal polyester.
  • The liquid crystal polyester composition is preferably prepared by melt-kneading a liquid crystal polyester, a fluorine resin, a carbon fiber, a granular filler, and a plate-like filler and other components used as necessary, using an extruder, extruding it in a strand shape, and pelletizing it.
  • The extruder used is preferably an extruder including a cylinder, one or more screws provided in the cylinder and one or more feed ports provided on the cylinder, more preferably such an extruder further including one or more vent parts provided in the cylinder.
  • The liquid crystal polyester composition of the present invention is excellent in slipperiness, thus preferably used in the material of a sliding member. Examples of the sliding member include bearing, slider, gear, cam and seal ring. Molding of the liquid crystal polyester composition into a sliding member is preferably performed by melt molding, and more preferably performed by injection molding.
  • EXAMPLES Production of Liquid Crystal Polyester
  • Into a reactor equipped with a stirrer, a torque meter, a nitrogen gas inlet, a thermometer and a reflux condenser, 1034.99 g (5.5 mol) of 6-hydroxy-2-naphthoic acid, 378.33 g (1.75 mol) of 2,6-naphthalene dicarboxylic acid, 83.07 g (0.5 mol) of terephthalic acid, 272.52 g (2.475 mol: excess of 0.225 molar, relative to the total amount of 2,6-naphthalene dicarboxylic acid and terephthalic acid) of hydroquinone, 1226.87 g (12 mol) of acetic anhydride, and 0.17 g of 1-methylimidazole as a catalyst were introduced. After the gas in the reactor was replaced with a nitrogen gas, in a nitrogen gas stream, the mixture was heated by raising the temperature from room temperature to 145° C. over 15 minutes under stirring, followed by reflux at 145° C. for 1 hour. Subsequently, the temperature was raised from 145° C. to 310° C. over 3 hours and 30 minutes while distilling off by-product acetic acid and unreacted acetic anhydride, and maintained at 310° C. for 3 hours, then the content of the reactor was taken out, and cooled to room temperature. The obtained solid was pulverized to a particle size of about 0.1 to 1 mm by a pulverizer, then, in a nitrogen atmosphere, the pulverized material was heated by raising the temperature from room temperature to 250° C. over 1 hour, then further raising it from 250° C. to 310° C. over 10 hours, and maintained at 310° C. for 5 hours to carry out solid phase polymerization of the material. After solid phase polymerization, the resultant was cooled to afford powdery liquid crystal polyester.
  • This liquid crystal polyester was found to have 55 mol % of a repeating unit (1) in which Ar1 is a 2,6-naphthylene group, 17.5 mol % of a repeating unit (2) in which Ar2 is a 2,6-naphthylene group, 5 mol % of a repeating unit (2) in which Ar2 is a 1,4-phenylene group, and 22.5% of a repeating unit (3) in which Ar3 is a 1,4-phenylene group, and X and Y are each oxygen atom, and have an incipient fluidization temperature of 333° C.
  • Fluorine Resin
  • As the fluorine resin, polytetrafluoroethylene (“Dyneon TF9205” of Sumitomo 3M) was used.
  • Carbon Fiber
  • As the carbon fiber, a chopped carbon fiber with a number-average fiber diameter of 7 μm and a number-average fiber length of 6 mm (“TR06UB4E” of MITSUBISHI RAYON CO., LTD.) was used.
  • Granular Filler
  • As the granular filler, following fillers were used.
      • Granular filler (1): Spherical alumina with a volume average particle diameter of 0.3 μm (“Sumicorundum AA-03” of Sumitomo Chemical Co., Ltd.
      • Granular filler (2): Spherical alumina with a volume average particle diameter of 2 μm (“Sumicorundum AA-2” of Sumitomo Chemical Co., Ltd.
      • Granular filler (3): Spherical alumina with a volume average particle diameter of 18 μm (“Sumicorundum AA-18” of Sumitomo Chemical Co., Ltd.
    Plate-Like Filler
  • As the plate-like filler, following fillers were used. Plate-like filler (1): Mica with a volume average particle diameter of 24 μm (“AB25S” of YAMAGUCHI MICA CO., LTD.) Plate-like filler (2): Graphite with a volume average particle diameter of 5 μm (“J-CPB” of Nippon Graphite Industories, ltd.) Plate-like filler (3): Graphite with a volume average particle diameter of 19 μm (“CPB” of Nippon Graphite Industories, ltd.) Plate-like filler (4): Graphite with a volume average particle diameter of 40 μm (“CB-150” of Nippon Graphite Industories, ltd.)
  • Examples 1 to 10, Comparative Example 1
  • A liquid crystal polyester, a fluorine resin, a carbon fiber, a granular filler and a plate-like filler were melt-kneaded at 320° C. in a ratio shown in Table 1, and pelletized, using a co-rotating twin-screw extruder (“PCM-30HS” of Ikegai Corp). The obtained pellet was injection molded at a cylinder nozzle temperature of 320° C., a mold temperature of 130° C., and an injection speed of 530 cm3/s, to obtain a molded body having a length of 126 mm, a width of 12.5 mm, and a thickness of 3.2 mm.
  • In the position of 50 mm from the gate of the long axis end face of the obtained molded body, a plate-like test piece having a width of 4 mm in the major axis and vertical direction was cut out. For this test piece, with the minimum area section (4 mm×3.2 mm) as a sliding surface, using a pin-on-disk type sliding test machine (Institut furVerbundwerkstoffe GmbH), with a high carbon chromium bearing steel (DIN [German Industrial Standard] 100Cr6 (surface roughness Ra of 0.2 μm) as a mating member, the friction and wear test was performed at 20° C., an applied pressure of 4 MPa, a rate of 1 m/s, for 20 hours, to obtain the friction coefficient and specific wear rate of the test piece and wear degree of the mating material.
  • As the friction coefficient of the test piece, the average value of the friction coefficient between 15 hours and 20 hours after the start of friction and wear test was obtained.
  • As the specific wear rate of the test piece, a value dividing the wear volume that is the product of the height difference and the area of the sliding surface of the test piece between 15 hours and 20 hours after the start of friction and wear test, by applied load and sliding distance was obtained.
  • As the wear degree of the mating member, the height difference between the sliding surface and the non-sliding surface of the mating material surface was measured, using White Light Profilometer (manufactured by FRT Microprof/Fries GmbH). The result is shown in Table 1.
  • TABLE 1
    Examples
    Comparative
    Example Example
    1 2 3 4 5 6 7 8 9 10 1
    Liquid crystal poly- (Part by mass) 100 100 100 100 100 100 100 100 100 100 100
    ester
    Fluorine resin (Part by mass) 15 15 7 15 15 15 16 16 16 16 14
    Carbon fiber (Part by mass) 22 19 28 18 22 22 22 22 22 22 29
    Granular filler (1) (Part by mass) 12 15 12 18 13 13 13 13
    Granular filler (2) (Part by mass) 12
    Granular filler (3) (Part by mass) 12
    Plate-like filler (1) (Part by mass) 6
    Plate-like filler (2) (Part by mass) 6
    Plate-like filler (3) (Part by mass) 6
    Plate-like filler (4) (Part by mass) 6
    Friction coefficient (—) 0.26 0.26 0.25 0.30 0.41 0.42 0.21 0.24 0.24 0.24 0.69
    of test piece
    Specific wear rate (×10−7 4.8 7.6 5.9 27.2 77.9 124.2 5.4 4.4 4.2 4.6 15.0
    of test piece mm3/Nm)
    Wear degree of mating (μm) 0 0 0 0 7 18 0 0 0 0 0
    material
  • INDUSTRIAL APPLICABILITY
  • The liquid crystal polyester composition of the present invention is excellent in slipperiness, thus is useful as a material of a sliding member.

Claims (12)

1. A liquid crystal polyester composition containing a liquid crystal polyester, a fluorine resin, a carbon fiber, and a granular filler.
2. The liquid crystal polyester composition according to claim 1, wherein the liquid crystal polyester has a repeating unit represented by formula (1), a repeating unit represented by formula (2), and a repeating unit represented by formula (3).
(1) —O—Ar1—CO—
(2) —CO—Ar2—CO—
(3) —X—Ar3—Y—
wherein Ar1 represents a phenylene group, a naphthylene group, or a biphenylylene group; Ar2 and Ar3 each independently represent a phenylene group, a naphthylene group, a biphenylylene group, or a group represented by formula (4); X and Y each independently represent an oxygen atom or an imino group; and each hydrogen atom present in the group represented by Ar1, Ar2 or Ar3 may be independently substituted with a halogen atom, an alkyl group or an aryl group;
(4) —Ar4—Z—Ar5
wherein Ar4 and Ar5 each independently represent a phenylene group or a naphthylene group; and Z represents an oxygen atom, a sulfur atom, a carbonyl group, a sulfonyl group or an alkylidene group.
3. The liquid crystal polyester composition according to claim 2, wherein the liquid crystal polyester has 30 to 80 mol % of the repeating unit represented by formula (1), 10 to 35 mol % of the repeating unit 4represented by formula (2), and 10 to 35 mol % of the repeating unit represented by formula (3), relative to a total amount of all repeating units of the liquid crystal polyester.
4. The liquid crystal polyester composition according to claim 1, wherein the granular filler is at least one granular filler selected from the group consisting of aluminum oxide, silicon oxide and titanium oxide.
5. The liquid crystal polyester composition according to claim 1, wherein a volume average particle diameter of the granular filler is 1 μm or less.
6. The liquid crystal polyester composition according to claim 1, wherein the fluorine resin comprises 5 to 20 parts by mass, relative to 100 parts by mass of the liquid crystal polyester.
7. The liquid crystal polyester composition according to claim 1, wherein the carbon fiber comprises 15 to 30 parts by mass, relative to 100 parts by mass of the liquid crystal polyester.
8. The liquid crystal polyester composition according to claim 1, wherein the granular filler comprises 5 to 20 parts by mass, relative to 100 parts by mass of the liquid crystal polyester.
9. The liquid crystal polyester composition according to claim 1, further containing a plate-shaped filler.
10. The liquid crystal polyester composition according to claim 9, wherein the plate-shaped filler is at least one selected from the group consisting of mica and graphite.
11. The liquid crystal polyester composition according to claim 9, wherein the plate-shaped filler comprises 5 to 10 parts by mass, relative to 100 parts by mass of the liquid crystal polyester.
12. A sliding member obtained by molding the liquid crystal polyester composition as defined in claim 1.
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