EP4273312A1 - Fabric, fabric object, and sheet - Google Patents

Fabric, fabric object, and sheet Download PDF

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Publication number
EP4273312A1
EP4273312A1 EP22746003.7A EP22746003A EP4273312A1 EP 4273312 A1 EP4273312 A1 EP 4273312A1 EP 22746003 A EP22746003 A EP 22746003A EP 4273312 A1 EP4273312 A1 EP 4273312A1
Authority
EP
European Patent Office
Prior art keywords
fabric
core
polyester
sheath
mass
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
EP22746003.7A
Other languages
German (de)
English (en)
French (fr)
Inventor
Kenichi Sakai
Nana TAKADA
Kenichi OKUNAGA
Takuya RYOMOTO
Takahiro Nishiguchi
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Toray Industries Inc
Original Assignee
Toray Industries Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Toray Industries Inc filed Critical Toray Industries Inc
Publication of EP4273312A1 publication Critical patent/EP4273312A1/en
Pending legal-status Critical Current

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Classifications

    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04B—KNITTING
    • D04B1/00—Weft knitting processes for the production of fabrics or articles not dependent on the use of particular machines; Fabrics or articles defined by such processes
    • D04B1/14—Other fabrics or articles characterised primarily by the use of particular thread materials
    • D04B1/16—Other fabrics or articles characterised primarily by the use of particular thread materials synthetic threads
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F8/00—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
    • D01F8/04—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers
    • D01F8/14—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers with at least one polyester as constituent
    • A—HUMAN NECESSITIES
    • A47—FURNITURE; DOMESTIC ARTICLES OR APPLIANCES; COFFEE MILLS; SPICE MILLS; SUCTION CLEANERS IN GENERAL
    • A47C—CHAIRS; SOFAS; BEDS
    • A47C31/00—Details or accessories for chairs, beds, or the like, not provided for in other groups of this subclass, e.g. upholstery fasteners, mattress protectors, stretching devices for mattress nets
    • A47C31/001—Fireproof means
    • A—HUMAN NECESSITIES
    • A47—FURNITURE; DOMESTIC ARTICLES OR APPLIANCES; COFFEE MILLS; SPICE MILLS; SUCTION CLEANERS IN GENERAL
    • A47C—CHAIRS; SOFAS; BEDS
    • A47C7/00—Parts, details, or accessories of chairs or stools
    • A47C7/02—Seat parts
    • A47C7/28—Seat parts with tensioned springs, e.g. of flat type
    • A47C7/282—Seat parts with tensioned springs, e.g. of flat type with mesh-like supports, e.g. elastomeric membranes
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F1/00—General methods for the manufacture of artificial filaments or the like
    • D01F1/02—Addition of substances to the spinning solution or to the melt
    • D01F1/07—Addition of substances to the spinning solution or to the melt for making fire- or flame-proof filaments
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F1/00—General methods for the manufacture of artificial filaments or the like
    • D01F1/02—Addition of substances to the spinning solution or to the melt
    • D01F1/10—Other agents for modifying properties
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/78—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolycondensation products
    • D01F6/82—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolycondensation products from polyester amides or polyether amides
    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04B—KNITTING
    • D04B1/00—Weft knitting processes for the production of fabrics or articles not dependent on the use of particular machines; Fabrics or articles defined by such processes
    • D04B1/14—Other fabrics or articles characterised primarily by the use of particular thread materials
    • D04B1/18—Other fabrics or articles characterised primarily by the use of particular thread materials elastic threads
    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04B—KNITTING
    • D04B1/00—Weft knitting processes for the production of fabrics or articles not dependent on the use of particular machines; Fabrics or articles defined by such processes
    • D04B1/22—Weft knitting processes for the production of fabrics or articles not dependent on the use of particular machines; Fabrics or articles defined by such processes specially adapted for knitting goods of particular configuration
    • D—TEXTILES; PAPER
    • D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B2331/00—Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products
    • D10B2331/04—Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products polyesters, e.g. polyethylene terephthalate [PET]
    • D—TEXTILES; PAPER
    • D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B2401/00—Physical properties
    • D10B2401/04—Heat-responsive characteristics
    • D—TEXTILES; PAPER
    • D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B2505/00—Industrial
    • D10B2505/08—Upholstery, mattresses

Definitions

  • the present invention relates to a fabric, a fabric body, and a seat. More particularly, the present invention relates to a fabric, a fabric body, and a seat having good sitting comfort, flame retardancy, and air permeability.
  • Patent Document 1 a fabric for attachment to a frame and a seating seat having the fabric attached to the frame have been developed.
  • Patent Document 1 JP 2019-143283 A
  • a fabric of the seating seat is required to be flame-retardant so that, for example, if a fire occurs, it will not spread.
  • Patent Document 1 does not disclose that the fabric and the seating seat provide flame retardancy.
  • the flame retardant may appear on a surface as scum during spinning and knitting steps. As a result, problems occur that an amount of the flame retardant contained in the fabric may vary, an appearance may become poor, and a desired flame retardancy cannot be provided.
  • the present invention has been made in view of such conventional problems, and it is an object of the present invention to provide a fabric, a fabric body, and a seat that exhibit excellent appearance, sitting comfort, and air permeability, and exhibit an excellent flame retardancy.
  • the fabric of one aspect of the present invention for solving the above-described problems comprises 50% by mass or more of monofilament, wherein the monofilament is a core-sheath composite fiber having a core and a sheath, wherein the core is contained in 60 to 90% by volume with respect to the core-sheath composite fiber and contains a first flame retardant and a polyester elastomer, and wherein the sheath is contained in 10 to 40% by volume with respect to the core-sheath composite fiber and consists of polyester excluding the polyester elastomer of the core.
  • the monofilament is a core-sheath composite fiber having a core and a sheath
  • the core is contained in 60 to 90% by volume with respect to the core-sheath composite fiber and contains a first flame retardant and a polyester elastomer
  • the sheath is contained in 10 to 40% by volume with respect to the core-sheath composite fiber and consists of polyester excluding the polyester elastomer
  • the fabric body of one aspect of the present invention for solving the above-described problems is a fabric body having the above-described fabric and a frame member.
  • the seat of one aspect of the present invention for solving the above-described problems is a seat using the above-described fabric body.
  • the fabric of one embodiment of the present invention comprises 50% by mass or more of monofilament.
  • the monofilament is a core-sheath composite fiber having a core and a sheath.
  • the core is contained in 60 to 90% by volume with respect to the core-sheath composite fiber and contains a first flame retardant and a polyester elastomer.
  • the sheath is contained in 10 to 40% by volume with respect to the core-sheath composite fiber and consists of polyester excluding the polyester elastomer of the core.
  • the fabric body of one embodiment of the present invention has the above-described fabric and a frame member. Each component will be described below.
  • the fabric comprises 50% by mass or more of monofilament.
  • the monofilament is a core-sheath composite fiber having a core and a sheath.
  • the core contains a first flame retardant and a polyester elastomer.
  • the polyester elastomer is not particularly limited.
  • the polyester elastomer is a thermoplastic polyester elastomer or the like.
  • a thermoplastic polyester elastomer resin may contain, as constituent components, for example, a high-melting point crystalline segment having a crystalline aromatic polyester as a main structural unit and a low-melting point polymer segment having an aliphatic polyether unit and/or an aliphatic polyester unit as a main structural unit.
  • the high-melting point crystalline segment is a polyester formed of an aromatic dicarboxylic acid or an ester-forming derivative thereof (hereinafter also referred to as an "acid component”) and a diol or an ester-forming derivative thereof (hereinafter also referred to as a "diol component").
  • the aromatic dicarboxylic acid include, for example, terephthalic acid, isophthalic acid, phthalic acid, naphthalene-2,6-dicarboxylic acid, naphthalene-2,7-dicarboxylic acid, anthracenedicarboxylic acid, diphenyl-4,4'-dicarboxylic acid, diphenoxyethanedicarboxylic acid, 4,4'-diphenyletherdicarboxylic acid, 5-sulfoisophthalic acid, sodium 3-sulfoisophthalate, and the like.
  • the aromatic dicarboxylic acid may be mainly used in the present embodiment. Some of the aromatic dicarboxylic acids may be replaced by an alicyclic dicarboxylic acid such as 1,4-cyclohexanedicarboxylic acid, cyclopentanedicarboxylic acid, and 4,4'-dicyclohexyldicarboxylic acid, or an aliphatic dicarboxylic acid such as adipic acid, succinic acid, oxalic acid, sebacic acid, dodecanedioic acid, and dimer acid.
  • An ester-forming derivative of dicarboxylic acid e.g., a lower alkyl ester, an aryl ester, a carbonic acid ester, an acid halide, etc. may also be used.
  • the diol is, for example, a diol having a molecular weight of 400 or less, or the like.
  • the diol having a molecular weight of 400 or less includes an aliphatic diol such as 1,4-butanediol, ethylene glycol, trimethylene glycol, pentamethylene glycol, hexamethylene glycol, neopentyl glycol, and decamethylene glycol; an alicyclic diol such as 1,1-cyclohexanedimethanol, 1,4-dicyclohexanedimethanol, and tricyclodecanedimethanol; an aromatic diol such as xylylene glycol, bis(p-hydroxy)diphenyl, bis(p-hydroxy)diphenylpropane, 2,2'-bis[4-(2-hydroxyethoxy)phenyl]propane, bis[4-(2-hydroxyethoxy)phenyl]sulfone, 1,1-bis[4-(2-hydroxyeth
  • the low-melting point polymer segment is at least one of an aliphatic polyether and an aliphatic polyester.
  • the aliphatic polyether includes ethylene oxide adducts of poly(oxyethylene) glycol, poly(oxypropylene) glycol, poly(oxytrimethylene) glycol, poly(oxytetramethylene) glycol, poly(oxyhexamethylene) glycol, and poly(oxypropylene) glycol, a copolymer of ethylene oxide and tetrahydrofuran, and the like.
  • the aliphatic polyether is preferably an ethylene oxide adduct of poly(oxytetramethylene) glycol and/or poly(oxypropylene) glycol and/or a copolymer of ethylene oxide and tetrahydrofuran.
  • the aliphatic polyester includes poly( ⁇ -caprolactone), polyenantholactone, polycaprylolactone, polybutylene adipate, polyethylene adipate, and the like.
  • the low-melting point polymer segment is preferably an ethylene oxide adduct of poly(oxytetramethylene) glycol or poly(oxypropylene) glycol, a copolymer glycol of ethylene oxide and tetrahydrofuran, poly( ⁇ -caprolactone), polybutylene adipate, polyethylene adipate, or the like, and more preferably an ethylene oxide adduct of poly(oxytetramethylene) glycol or poly(oxypropylene) glycol, or a copolymer glycol of ethylene oxide and tetrahydrofuran, from the viewpoint that a polyester block copolymer obtained has an excellent elastic property.
  • a number average molecular weight of the low-melting point polymer segment is preferably 300 to 6000, and more preferably 1000 to 3000, in a copolymerized state.
  • the number average molecular weight of the low-melting point polymer segment is within the above-described ranges, a fabric obtained has an excellent fatigue resistance, thus improving durability to exhibit a more excellent sitting comfort.
  • polyester block copolymers (a polyester block copolymer (A1) and a polyester block copolymer (A2)) are preferably used, from the viewpoints of an effect of improving flame retardancy by improving dispersibility of a flame retardant and that stretchability and heat shrinkability of a filament can be improved.
  • the polyester block copolymer (A1) contains, as constituent components, for example, a high-melting point crystalline segment (H1) having a crystalline aromatic polyester as a main structural unit and a low-melting point polymer segment (L1) having an aliphatic polyether unit and/or an aliphatic polyester as a main structural unit.
  • H1 high-melting point crystalline segment
  • L1 low-melting point polymer segment
  • the high-melting point crystalline segment (H1) may be composed of one selected from the above-described acid components and one or more selected from the above-described diol components.
  • the high-melting point crystalline segment (H1) is, for example, a polybutylene terephthalate unit derived from terephthalic acid or dimethyl terephthalate and 1,4-butanediol.
  • the low-melting point polymer segment (L1) may be selected from the above-described aliphatic polyethers and/or aliphatic polyesters.
  • a compounding ratio of the high-melting point crystalline segment (H1) to the low-melting point polymer segment (L1) in the polyester block copolymer (A1) is preferably 50 to 95% by mass of the high-melting point crystalline segment (H1) to 5 to 50% by mass of the low-melting point polymer segment (L1), more preferably 65 to 95% by mass of the high-melting point crystalline segment (H1) to 5 to 35% by mass of the low-melting point polymer segment (L1), and further preferably 80 to 95% by mass of the high-melting point crystalline segment (H1) to 5 to 20% by mass of the low-melting point polymer segment (L1).
  • the compounding ratio of the high-melting-point crystalline segment (H1) to the low-melting-point polymer segment (L1) is within the above-described ranges, a fabric body obtained has an excellent balance between heat resistance and durability with processability.
  • a melting point of the polyester block copolymer (A1) is preferably 200°C to 225°C, and more preferably 210°C to 225°C. When the melting point of the polyester block copolymer (A1) is within the above-described ranges, a polyester elastomer obtained has sufficient rigidity and heat resistance and has an excellent fatigue resistance.
  • the polyester block copolymer (A2) contains, as constituent components, a high-melting point crystalline segment (H2) having a crystalline aromatic polyester as a main structural unit and a low-melting point polymer segment (L2) having an aliphatic polyether unit and/or an aliphatic polyester as a main structural unit.
  • the high-melting point crystalline segment (H2) may be composed of two or more selected from the above-described acid components and one or more selected from the above-described diol components.
  • the high-melting point crystalline segment (H2) include, for example, a combination of terephthalic acid and isophthalic acid, a combination of terephthalic acid and dodecanedioic acid, a combination of terephthalic acid and dimer acid, and the like.
  • a polyester elastomer obtained can improve dispersibility of a flame retardant and suppress aggregation of flame retardants. As a result, the polyester elastomer easily improves in flame retardancy. Moreover, the polyester elastomer may improve stretchability and heat shrinkability of a filament.
  • the high-melting point crystalline segment (H2) preferably consists of a polybutylene terephthalate unit derived from terephthalic acid and/or dimethyl terephthalate and a polybutylene isophthalate unit derived from isophthalic acid and/or dimethyl isophthalate and 1,4-butanediol.
  • the low-melting point polymer segment (L2) may be selected from the above-described aliphatic polyethers and/or aliphatic polyesters.
  • a compounding ratio of the high-melting point crystalline segment (H2) to the low-melting point polymer segment (L2) in the polyester block copolymer (A2) is preferably 40 to 90% by mass of the high-melting point crystalline segment (H2) to 10 to 60% by mass of the low-melting point polymer segment (L2), more preferably 45 to 85% by mass of the high-melting point crystalline segment (H2) to 15 to 55% by mass of the low-melting point polymer segment (L2), and further preferably 70 to 85% by mass of the high-melting point crystalline segment (H2) to 15 to 30% by mass of the low-melting point polymer segment (L2).
  • a melting point of the polyester block copolymer (A2) is preferably 120°C to 170°C, and more preferably 130°C to 165°C.
  • the polyester block copolymer (A2) contributes to improvement of dispersibility of a flame retardant or the like when used in combination with the polyester block copolymer (A1).
  • a fabric body obtained does not impair heat shrinkability and has excellent abrasion resistance, toughness, flame retardancy, and appearance.
  • a compounding amount (part by mass) of the polyester block copolymer (A1) and the polyester block copolymer (A2) is preferably 50 to 99 parts by mass of the polyester block copolymer (A1) and 1 to 50 parts by mass of the polyester block copolymer (A2), more preferably 60 to 95 parts by mass of the polyester block copolymer (A1) and 5 to 40 parts by mass of the polyester block copolymer (A2), and further preferably 70 to 95 parts by mass of the polyester block copolymer (A1) and 5 to 30 parts by mass of the polyester block copolymer (A2).
  • a polyester elastomer obtained has an excellent fatigue resistance and has excellent toughness and flame retardancy due to improvement of dispersibility of a flame retardant.
  • the polyester block copolymer (A1) and the polyester block copolymer (A2) can be produced by known methods.
  • the polyester block copolymer (A1) and the polyester block copolymer (A2) may be produced by a method of transesterifying a lower alcohol diester of a dicarboxylic acid with an excessive amount of a low molecular weight glycol and a low-melting point polymer segment component in presence of a catalyst and polycondensing the obtained reaction product, a method of esterifying a dicarboxylic acid with an excess amount of glycol and a low-melting point polymer segment component in presence of a catalyst and polycondensing the obtained reaction product, and the like.
  • additives such as antioxidants (a phosphonite compound, a phosphorous compound, a hypophosphorous compound, a hindered phenol-based compound, a thioether-based compound, etc.), UV absorbers (benzotriazole-based, benzophenone-based, etc.), light stabilizers (HALS: hindered amine-based compound, etc.), antistatic agents (a polyether ester amide, etc.), lubricants (a stearyl alcohol, a stearic acid metal salt, a stearic acid amide, a stearic acid glyceride, etc.), dyes (organic dyes such as nigrosine), pigments (carbon black , titanium dioxide, etc.), plasticizing agents (phthalic acid-based, adipic acid-based, trimellitic acid-based, etc.), release agents (a paraffin wax, saturated fatty acid ester-based, unsaturated fatty acid ester
  • Examples of a phosphorus-containing compound include a hydrate of metal hypophosphite, in addition to an organic phosphorus-containing compound exemplified as a flame retardant.
  • a phosphorus-containing compound examples include a hydrate of metal hypophosphite, in addition to an organic phosphorus-containing compound exemplified as a flame retardant.
  • the polyester elastomer easily suppresses oxidative deterioration and easily improves surface appearance and color tone.
  • the first flame retardant is a flame retardant contained in a core.
  • the first flame retardant preferably contains at least one selected from the group consisting of an organic phosphate compound, a metal phosphinate, and a triazine skeleton-containing compound.
  • the organic phosphate compound includes, for example, tetrakis(2,6-dimethylphenyl) 1,3-phenylene bisphosphate, and resorcinol bis(diphenyl phosphate), as resorcinol phosphates; hydroquinone bis(diphenyl phosphate) as hydroquinone phosphates; biphenol bis(diphenyl phosphate) as biphenol phosphates; bisphenol-A bis(diphenyl phosphate) as bisphenol phosphates; and the like.
  • the organic phosphate compound exhibits a melting point lower than that of a general thermoplastic polyester elastomer and further has a good compatibility with a polyester elastomer. Therefore, the organic phosphate compound has an excellent dispersibility during melt-kneading. In addition, the organic phosphate compound may improve flame retardancy of the polyester elastomer and suppress deterioration of mechanical strength property.
  • organic phosphate compound an aryl spirodiphosphinate condensed with a polyhydric alcohol such as pentaerythritol is also appropriately used.
  • a diphosphinate compound having a spiro-type ring-fused structure exhibits a high melting point, easily improves in dispersibility to a polyester elastomer, and has a high heat resistance. Therefore, the diphosphinate compound having a spiro-type ring-fused structure is more appropriately used since it can suppress bleeding out during processing.
  • a melting point of the aryl spirodiphosphinate is preferably 100 to 300°C.
  • the aryl spirodiphosphinate is less likely to bleed out during melt processing and has excellent dispersibility and processability during melt processing.
  • a filament or a molded article obtained easily improves in toughness, fatigue resistance, and surface appearance.
  • An acid value of the aryl spirodiphosphinate is preferably 1.0 mgKOH/g or less, and more preferably 0.5 mgKOH/g or less.
  • a polyester elastomer obtained has excellent flame retardancy and hue.
  • a filament using the obtained polyester elastomer easily suppresses deterioration of heat aging resistance and hydrolysis resistance.
  • the aryl spirodiphosphinate is, for example, a pentaerythritol diphosphinate compound or the like.
  • the pentaerythritol diphosphinate compound includes 2,4,8,10-tetraoxa-3,9-diphosphaspiro[5.5]undecane,3,9-dibenzyl-3,9-dioxide, 2,4,8,10-tetraoxa-3,9-diphosphaspiro[5.5]undecane,3,9-di ⁇ -methylbenzyl-3,9-dioxide, 2,4,8,10-tetraoxa-3,9-diphosphaspiro[5.5]undecane,3,9-di(2-phenylethyl)-3,9-dioxide, 2,4,8,10-tetraoxa-3,9-diphosphaspiro[5.5]undecane,3,9-bis(diphenylmethyl)-3,9-dioxide, and the
  • a content of the organic phosphate compound is preferably 1% by mass or more, and more preferably 10% by mass or more, based on the entire core. Moreover, the content of the organic phosphate compound is preferably 30% by mass or less, and more preferably 20% by mass or less, based on the entire core. When the content of the organic phosphate compound is within the above-described ranges, a fabric body obtained does not impair heat shrinkability and has excellent toughness, flame retardancy, and appearance.
  • R 1 and R 2 are organic groups which may be the same or different, and R3 is methylene, ethylene, n-propylene, isopropylene, n-butylene, t-butylene, phenylene, or naphthylene and may have various substituents on its aromatic ring.
  • M is aluminum, zinc, calcium, or magnesium.
  • the metal phosphinate (also referred to as a metal phosphinate compound) include a metal phosphinate substituted with an aliphatic hydrocarbon group, such as a metal salt of diethylphosphinate and a metal salt of methylethylphosphinate, preferably an aluminum phosphinate (aluminum diethylphosphinate) or a zinc phosphinate (zinc diethylphosphinate).
  • the metal phosphinate is more preferably an aluminum phosphinate, since it can significantly improve flame retardancy of a polyester elastomer and suppress bleed-out during processing.
  • a content of the metal phosphinate is preferably 1% by mass or more, and more preferably 10% by mass or more, based on the entire core. Moreover, the content of the metal phosphinate is preferably 30% by mass or less, and more preferably 20% by mass or less, based on the entire core. When the content of the metal phosphinate is within the above-described ranges, a polyester elastomer obtained has an excellent flame retardancy and an excellent processability.
  • the organic phosphorus-containing compound and the metal phosphinate are melt-kneaded together with the polyester elastomer described above in a specific range to prepare a flame-retardant masterbatch in advance, and further the flame-retardant masterbatch is melt-kneaded with the polyester elastomer, so that aggregation of organic phosphorus-containing compounds can be suppressed, deterioration of mechanical property can be suppressed, and a flame-retardant polyester elastomer resin composition and a flame-retardant polyester elastomer filament which have excellent flame retardancy, surface appearance, surface smoothness, toughness, and fatigue resistance can be obtained.
  • thermoplastic resin used in preparing a masterbatch containing an organic phosphorus-containing compound may be the polyester elastomer described above, and a thermoplastic polyester resin such as polyethylene terephthalate (PET), polybutylene terephthalate (PBT), polyethylene naphthalate (PEN), and polybutylene naphthalate (PBN) may be used.
  • PET polyethylene terephthalate
  • PBT polybutylene terephthalate
  • PEN polyethylene naphthalate
  • PBN polybutylene naphthalate
  • organic phosphorus-containing compound may be used together with a polyester elastomer in molding a masterbatch.
  • the thermoplastic polyester elastomer and the organic phosphorus-containing compound contained in the masterbatch are preferably melt-kneaded with a compositional ratio in a range of 100 parts by mass of the polyester elastomer to 10 to 100 parts by mass of the organic phosphorus-containing compound from the viewpoint that deterioration of processability of a polyester elastomer obtained is suppressed to obtain an excellent flame retardancy, and they are more preferably melt-kneaded with a compositional ratio in a range of 100 parts by mass of the polyester elastomer to 20 to 70 parts by mass of the organic phosphorus-containing compound from the viewpoint that aggregation of organic phosphorus-containing compounds is suppressed to improve surface appearance and surface smoothness.
  • the triazine skeleton-containing compound is, for example, melamine cyanurate, melamine, cyanuric acid, isocyanuric acid, a triazine derivative, an isocyanurate derivative, or the like, preferably melamine cyanurate.
  • Melamine cyanurate is preferably in a form of a particle (powder). Moreover, melamine cyanurate may be untreated or surface-treated with a coupling agent (particularly a silane coupling agent).
  • triazine skeleton-containing compound a group of compounds having a triazine ring in a hindered amine structure which is generally used as a radical scavenger can also be appropriately used.
  • a triazine ring-containing hindered amine compound By adding a triazine ring-containing hindered amine compound to a polyester elastomer, not only a general effect of improving weather resistance but also an effect of improving flame retardancy can be obtained.
  • the triazine skeleton-containing compound has the hindered amine structure
  • aggregation of triazine rings can be suppressed to improve dispersibility of the triazine skeleton-containing compound. This improves surface appearance, surface smoothness, toughness, and fatigue resistance of a polyester elastomer obtained.
  • the hindered amine compound is preferably a triazine ring-containing N-alkoxy hindered amine compound.
  • the triazine ring-containing N-alkoxy hindered amine compound generates a nitroxide radical having a higher radical scavenging ability during combustion than a N-H type hindered amine compound and a N-R type hindered amine compound, and easily improves in flame retardancy compared with an alkyl-substituted type hindered amine compound.
  • the triazine ring-containing N-alkoxy hindered amine compound includes 1,5,8,12-tetrakis[2,4-bis(N-butyl-N-(2,2,6,6-tetramethyl-4-piperidyl)amino)-1,3,5-triazin-6-yl]-1,5,8,12-tetraazadodecane, 1,5,8,12-tetrakis[2,4-bis(N-butyl-N-(2,2,6,6-tetramethyl-4-piperidyl)amino)-1,3,5-triazin-6-yl]-1,12-dimethyl-1,5,8,12-tetraazadodecane, and the like, and includes, as commercially available products, Flamestab NOR116FF manufactured by BASF Japan Ltd., and the like.
  • a content of the triazine skeleton-containing compound is preferably 1% by mass or more, and more preferably 3% by mass or more, based on the entire core. Moreover, the content of the triazine skeleton-containing compound is preferably 30% by mass or less, and more preferably 10% by mass or less, based on the entire core. When the content of the triazine skeleton-containing compound is within the above-described ranges, a polyester elastomer obtained has an excellent flame retardancy and has excellent toughness, fatigue resistance, and surface appearance.
  • a total compounding amount of the organic phosphate compound, the metal phosphinate, and the triazine skeleton-containing compound is preferably 1% by mass or more, and more preferably 10% by mass or more, based on the entire core. Moreover, the total compounding amount of the organic phosphate compound, the metal phosphinate, and the triazine skeleton-containing compound is preferably 30% by mass or less, and more preferably 20% by mass or less, based on the core.
  • a fabric body obtained becomes less likely to generate scum in the spinning step, the knitting step, and the like, and exhibits a more stable and excellent flame retardancy.
  • a content of the core may be 60% or more by volume, preferably 70% or more by volume, based on the core-sheath composite fiber. Moreover, the content of the core may be 90% or less by volume, more preferably 80% or less by volume, based on the core-sheath composite fiber.
  • a fabric body obtained does not impair heat shrinkability and exhibits a more excellent sitting comfort.
  • the content of the core is 90% or less by volume, a fabric body obtained becomes less likely to generate scum in the spinning step, the knitting step, and the like, and exhibits a more stable and excellent flame retardancy.
  • the sheath contains polyester excluding the above-described polyester elastomers contained in the core. Moreover, the sheath appropriately contains a second flame retardant.
  • the polyester other than the polyester elastomers contained in the core is not particularly limited.
  • the polyester other than the polyester elastomers contained in the core is polyethylene terephthalate (PET), polybutylene terephthalate (PBT), polyethylene naphthalate (PEN), polybutylene naphthalate (PBN), or the like.
  • PET polyethylene terephthalate
  • PBT polybutylene terephthalate
  • PEN polyethylene naphthalate
  • PBN polybutylene naphthalate
  • the polyester other than the polyester elastomers contained in the core is preferably PET from the viewpoint of productivity.
  • the sheath preferably contains a second flame retardant.
  • the second flame retardant is not particularly limited.
  • the second flame retardant preferably contains at least one of an aryl phosphinic acid compound and an alkyl phosphinic acid compound.
  • at least one of the aryl phosphinic acid compound and the alkyl phosphinic acid compound is more preferably copolymerized with the above-described polyester.
  • the second flame retardant is an aryl phosphinic acid compound or an alkyl phosphinic acid compound, it is further preferable that they are added to a polymerization system prior to polycondensation after transesterification or during an initial stage of a polycondensation reaction and copolymerized in a polyester main chain.
  • the aryl phosphinic acid compound is not particularly limited.
  • the aryl phosphinic acid compound is 2-carboxyethyl(phenyl)phosphinic acid, 2-carboxyethyl(naphthyl)phosphinic acid, 2-carboxyethyl(toluyl)phosphinic acid, or the like.
  • the aryl phosphinic acid compound is preferably 2-carboxyethyl(phenyl)phosphinic acid.
  • the alkyl phosphinic acid compound is not particularly limited.
  • the alkyl phosphinic acid compound is 2-carboxyethylmethylphosphinic acid, 2-carboxyethyl-tert-butylphosphinic acid, or the like.
  • the alkyl phosphinic acid compound is preferably 2-carboxyethylmethylphosphinic acid.
  • a content of the second flame retardant is preferably 0.3% by mass or more, more preferably 0.5% by mass or more, and further preferably 0.6% by mass or more, in terms of phosphorus element, based on the sheath. Moreover, the content of the second flame retardant is preferably 1.1% by mass or less, more preferably 1.0% by mass or less, and further preferably 0.9% by mass or less, in terms of phosphorus element, based on the sheath. When the content of the second flame retardant is within the above-described ranges, a fabric body obtained becomes less likely to generate scum in the spinning step, the knitting step, and the like, and exhibits a more stable and excellent flame retardancy.
  • a content of the sheath may be 10% or more by volume, preferably 20% or more by volume, based on the core-sheath composite fiber. Moreover, the content of the sheath may be 40% or less by volume, more preferably 30% or less by volume, based on the core-sheath composite fiber.
  • the content of the sheath is 10% or more by volume, a fabric body obtained becomes less likely to generate scum in the spinning step, the knitting step, and the like, and exhibits a more stable and excellent flame retardancy.
  • the content of the sheath is 40% or less by volume, deterioration of heat shrinkability of a fabric body obtained can be suppressed.
  • a content of the monofilament in the fabric may be 50% by mass or more, preferably 60% by mass or more, and more preferably 70% by mass or more.
  • a fabric body obtained exhibits an appropriate amount of deflection when attached to a frame member.
  • a fineness of the monofilament is preferably 300 dtex or more, and more preferably 500 dtex or more. Moreover, the fineness of the monofilament is preferably 3000 dtex or less, and more preferably 2000 dtex or less. When the fineness of the monofilament is 300 dtex or more, a fabric has an excellent strength. On the other hand, when the fineness of the monofilament is 3000 dtex or less, the monofilament has an excellent process passing property. Besides, the fineness of the monofilament may be calculated based on JIS L 1018 (2010) 8.7.1.
  • a dry heat shrinkage of the monofilament is preferably 5.0% or more, more preferably 10.0% or more, and further preferably 20.0% or more. Moreover, the dry heat shrinkage of the monofilament is preferably 50.0% or less, more preferably 45.0% or less, and further preferably 40.0% or less.
  • a fabric obtained shrinks appropriately by being applied with heat and is easily attached to the frame member. In addition, the fabric is easily adjusted to have an appropriate amount of deflection when attached to the frame member.
  • a dry heat shrinkage of a fiber can be adjusted depending on a base polymer constituting the fiber, a core-sheath ratio, a type of a flame retardant, an amount of the flame retardant added, a spinning condition, and the like.
  • a monofilament that is also a core-sheath composite fiber containing a polyester elastomer with a fineness of 300 to 3000 dtex adjusted to a dry heat shrinkage of 5.0 to 50.0% can be appropriately used for the fabric body of the present invention.
  • the dry heat shrinkage may be measured based on JIS L 1013 (8.18.2) (2010) B method (filament shrinkage rate).
  • a melting point of the core-sheath composite fiber constituting the monofilament is not particularly limited.
  • the melting point of the core-sheath composite fiber is preferably 200°C or higher, and more preferably 225°C or higher.
  • the melting point of the core-sheath composite fiber is preferably 280°C or lower, and more preferably 260°C or lower.
  • a melting point of the core is not particularly limited.
  • the melting point of the core is preferably 200°C or higher, and more preferably 210°C or higher.
  • the melting point of the core is preferably 230°C or lower, and more preferably 220°C or lower.
  • a melting point of the sheath is not particularly limited.
  • the melting point of the sheath is preferably 225°C or higher, and more preferably 235°C or higher.
  • the melting point of the sheath is preferably 280°C or lower, and more preferably 260°C or lower.
  • a method of producing a monofilament that is also a core-sheath composite fiber is not particularly limited.
  • the monofilament can be produced by a core-sheath composite spinning method using conventionally known co-extrusion equipment. According to the core-sheath composite spinning method, the monofilament may be produced with high productivity and at low cost.
  • a first flame retardant and a polyester elastomer constituting a core and a polyester constituting a sheath are molten in separate extruders, and then weighed by a gear pump and flowed into a composite pack, respectively.
  • the two types of polymers that constitute the core and the sheath flowed into the composite pack are filtered through a metal non-woven fabric filter or a metal mesh in the pack, and then introduced into a composite spinneret and spun with the core being surrounded by the sheath.
  • a master chip containing large amounts of a pigment, a light resistance agent, an antibacterial agent, etc. as desired is prepared, and necessary amounts of these components can be mixed with the first flame retardant and the polyester elastomer constituting the core and/or the polyester constituting the sheath to perform spinning.
  • a molten monofilament spun from the composite spinneret is cooled, extended, and heat-set according to a standard method, so that a monofilament that is also a core-sheath composite fiber may be produced efficiently.
  • a fabric may contain fibers other than the above-described monofilaments.
  • fibers other than monofilaments are synthetic fibers that are multifilaments.
  • a multifilament of polyester fibers, a multifilament of polyamide fibers, and the like are appropriate as the fibers.
  • the multifilament may be a textured yarn subjected to processing such as false twisting.
  • fibers other than monofilaments are preferably false-twisted PET from the viewpoint of improving texture and feeling of touch of the fabric and from the viewpoint of productivity.
  • a content of fibers other than monofilaments is less than 50% by mass, preferably 40% by mass or less.
  • the fabric may be knitted or woven.
  • the fabric of the present embodiment is preferably a knitted fabric because it exhibits an excellent sitting comfort as it has an excellent stretchability, has improved air permeability, and has a wide variety of pattern expressions.
  • the knitted fabric preferably has a knitting density of 10 yarns/25.4 mm or more, and more preferably 15 yarns/25.4 mm or more, in at least one of a warp direction and a weft direction. Moreover, the knitting density is preferably 50 yarns/25.4 mm or less, and more preferably 40 yarns/25.4 mm or less. When the knitting density is within the above-described ranges, a fabric (knitted fabric) having an appropriate amount of deflection and strength when attached to the frame member is easily obtained. As a result, a fabric body obtained exhibits more excellent sitting comfort and air permeability.
  • An amount of deflection of the fabric when a load of 400 N is applied to the central part thereof is preferably 20 mm or more, and more preferably 30 mm or more. Moreover, the amount of deflection is preferably 60 mm or less, and more preferably 50 mm or less.
  • a fabric body obtained using the fabric may have an appropriate range of an amount of deflection when a load is applied to a support surface that supports a user (for example, when the fabric body is a backrest of a sitting seat, or seat base). As a result, the fabric body obtained has an excellent sitting comfort. In addition, the fabric body obtained may retain a moderate elasticity.
  • the central part of the fabric refers to a center of gravity of a planar shape of a fabric. That is, for example, when the fabric has a polygonal shape, the center of gravity of the polygonal shape becomes a central part of the fabric.
  • air permeability of the fabric is preferably 5 cm 3 /cm 2 /sec or more, and more preferably 20 cm 3 /cm 2 /sec or more. Moreover, air permeability of the fabric is preferably 300 cm 3 /cm 2 /sec or less, and more preferably 180 cm 3 /cm 2 /sec or less.
  • air permeability of the fabric is within the above-described ranges, a fabric body obtained can have a reduced stuffy feeling and sufficiently support a body when used by a user.
  • air permeability may be measured based on JIS L 1096 (8.27.1) (2010) A method (Frazier type method).
  • the fabric of the present embodiment contains a first flame retardant at the core of the core-sheath composite fiber that constitutes the monofilament.
  • a first flame retardant contained in the core does not easily generate scum in steps such as a spinning step and a knitting step.
  • a fabric obtained exhibits an excellent appearance and also exhibits an excellent flame retardancy.
  • flammability of the fabric preferably has a burn rate of 0 mm/min in FMVSS 302 (horizontal method). This indicates that the fabric will extinguish itself before an A marker line. When the burn rate is 0 mm/min in FMVSS 302 (horizontal method), the fabric exhibits selfextinguishing property and thus has an excellent flame retardancy.
  • a judgment grade by a 20 mm vertical combustion test is more preferably V-0.
  • the judgment grade is V-0 in the 20 mm vertical combustion test (UL94V test)
  • the fabric has an excellent flame retardancy.
  • the frame member is not specifically limited.
  • the frame member is a member having strength enough to withstand tension of the fabric when the fabric is fixed under tension in at least one direction.
  • the frame member is made of a metal such as iron, aluminum, and titanium, carbon, wood, plastic, or the like.
  • the frame member is preferably made of metal or carbon from the viewpoint of high strength, and more preferably made of carbon from the viewpoint of weight reduction.
  • FIG. 1 is a schematic view for explaining a method of attaching a frame member to a fabric.
  • FIG. 2 is a schematic view of a fabric body.
  • a fabric 1 is a bag-shaped knitted fabric processed into a three-dimensional shape so that a frame member 2 can be inserted therein.
  • the knitted fabric can be knitted using a weft knitting machine.
  • a weft knitting structure is not particularly limited.
  • the weft knitting structure is a jersey structure, a garter structure, a smooth structure, a rib structure, or the like.
  • the fabric 1 is formed with an opening 1a for inserting the frame member.
  • frame members disassembled into two parts are inserted from the opening 1a and assembled to form a frame member 2 in a substantially rectangular shape in the fabric 1.
  • the fabric 1 is thermally shrunk to closely attach to the frame member 2 by, for example, performing heat treatment, as shown in FIG. 2 .
  • a non-sewn and non-bonded fabric body 3 may be formed.
  • the non-sewn and non-bonded fabric body can be used in various applications where it is desirable to form a three-dimensional fabric surface, despite being non-sewn and non-bonded.
  • the fabric body of the present embodiment is not particularly limited.
  • the fabric body is appropriate for various types of seats, since it maintains an excellent flame retardancy and exhibits excellent sitting comfort and air permeability. More specifically, the fabric body is appropriate for a seat surface, a backrest, etc., such as a seat for an office chair, a car seat, and a seat for a railroad vehicle.
  • the present invention is not particularly limited to the above-described embodiment. Besides, the above-described embodiment mainly describes an invention having the following configurations.
  • the first flame retardant contained in the core is less likely to appear as scum in a spinning step or a knitting step.
  • the fabric has an excellent appearance and easily maintains an excellent flame retardancy.
  • the fabric exhibits excellent sitting comfort and air permeability.
  • the fabric exhibits more excellent seating comfort and air permeability.
  • the first flame retardant contains at least one selected from the group consisting of an organic phosphate compound, a metal phosphinate, and a triazine skeleton-containing compound, which is contained in an amount of 1 to 30% by mass based on the core.
  • the fabric becomes less likely to generate scum in the spinning step, the knitting step, and the like, and exhibits a more stable and excellent flame retardancy.
  • the fabric becomes less likely to generate scum in the spinning step, the knitting step, and the like, and exhibits a more stable and excellent flame retardancy.
  • a fabric body having the fabric of any one of (1) to (4) and a frame member.
  • the fabric body has an excellent appearance and easily maintains an excellent flame retardancy.
  • the fabric body exhibits excellent sitting comfort and air permeability.
  • the fabric can be used in various applications where it is desirable to form a three-dimensional fabric surface, despite being non-sewn and non-bonded.
  • the seat easily maintains an excellent flame retardancy.
  • the seat exhibits excellent sitting comfort and air permeability.
  • a monofilament was taken from a fabric and cut in a direction perpendicular to a fiber axis to observe a cut surface obtained using a digital microscope (VHX-6000, manufactured by KEYENCE CORPORATION), diameters of a core and a sheath were measured using a length measurement tool of the digital microscope, and a volume ratio % of the core and a volume ratio % of the sheath were calculated from a cross-sectional area of the monofilament and respective cross-sectional areas of the core and the sheath using an area measurement tool of the digital microscope.
  • the ratios were calculated from an average value with the number of observation samples being as 10. Besides, figures below the first decimal place were rounded off.
  • An extreme value of a heat-fusing curve was measured for 10 mg of a monofilament sample taken from a fabric at a temperature rising rate of 10 °C/min from 30°C to 280°C using a differential scanning calorimeter DSC-7 manufactured by PerkinElmer Co., Ltd., and the temperature giving the obtained extreme value of the heat-fusing curve was taken as each melting point.
  • a dry heat shrinkage of a monofilament was measured based on JIS L 1013 (8.18.2) (2010) B method (filament shrinkage rate).
  • An initial load was applied to the sample, 500 mm of which was accurately measured to make two points of marks, and after removing the initial load, the sample was left in a dryer set at 185°C while being hung for 15 minutes and then taken out. After cooling to room temperature, an initial load is applied again to the sample, a length (mm) of which between the two points was measured, and a dry heat shrinkage (%) was measured by the following equation ((500 - length between the two points after heat treatment)/500 ⁇ 100) to calculate an average value of 5 time measurement.
  • the initial loads were set in accordance with JIS L 1013 (8.5.1) depending on a fineness of the sample, respectively.
  • the number of occurrences of bump yarn was expressed by a total weight (kg) of extruded polymers/1000 kg ⁇ the number of occurrences of bump yarn.
  • Air permeability was measured based on JIS L 1096 (8.27.1) (2010) A method (Frazier type method).
  • a test piece of 20 cm ⁇ 20 cm was taken from five different sites on a fabric, and the test piece was attached to one end (intake side) of a cylinder using a Frazier type tester. In attaching the test piece, the test piece was placed on the cylinder, and a load of about 98 N (10 kgf) was evenly applied from the top of the test piece so as not to block the intake part to prevent air leakage at the mounting part of the test piece.
  • a suction fan was adjusted so that a tilt-type barometer indicated a pressure of 125 Pa by a rheostat, and an amount of air passing through the test piece was measured with the table attached to the tester from a pressure indicated by a vertical-type barometer and a type of an air hole used at that time to calculate an average value for the measurements for five test pieces.
  • an amount of deflection when a load of 400 N was applied was measured using a seat static load deflection tester (FGS-TV, manufactured by NIDEC DRIVE TECHNOLOGY CORPORATION). Specifically, the fabric was stretched in a tense state over a frame member made of metal to obtain a fabric body.
  • FGS-TV seat static load deflection tester
  • the fabric body was placed on a fixing jig with a height of 30 cm and applied with an initial load of 5 N by a pressure plate having a horizontally long oval shape and a width of 250 mm ⁇ 300 mm so that the load center of the pressure plate was overlapped with the central part of the fabric to define the load center of the pressure plate at that time as a starting point.
  • the fabric body was applied with a load up to 900 N at a speed of 50 mm/min, as precompression, then unloaded at a speed of 50 mm/min, and left for 1 minute, followed by similarly applied with a load up to 900 N and then unloaded at a speed of 50 mm/min to measure an amount of deflection from the starting point when each load was applied at that time.
  • the "amount of deflection when a load of 400 N is applied" here refers to an amount of deflection from the starting point when a load of 400 N is applied to the fabric body.
  • directionality of the fabric when fixing the fabric body on a frame fixing jig, which may be any of a vertical direction and a horizontal direction.
  • test pieces each having a size of 250 mm in length and 120 mm in width were randomly taken from a fabric in vertical and horizontal directions, respectively. Next, they were evaluated based on FMVSS 302 (horizontal method). The test pieces were pinched with a special jig, placed horizontally, and flame-contacted at the ends thereof with a 38 mm flame for 15 seconds to measure burn times (sec) until reaching 254 mm between an A standard line and a B standard line, or if not reaching the B standard line, burn distances (mm) and burn times (sec) thereof. Moreover, if not reaching the A standard line, burn distances and burn times were recorded as 0 mm and 0 second, respectively.
  • burn rates were calculated for the vertical and horizontal directions of the fabric using the equation 1 below, respectively.
  • the "flammability (horizontal method)" refers to an average value of burn rates of three test pieces each in the vertical and horizontal directions of the fabric.
  • Burn rate mm / min burn distance mm / burn time seconds ⁇ 60
  • test pieces each having a size of 125 mm in length and 13 mm in width were randomly taken from a fabric in vertical and horizontal directions, respectively. Next, they were evaluated based on a 20 mm vertical combustion test (UL94V test) in the UL94 standard.
  • UL is a safety standard for an electronic equipment as established and approved by Underwriters Laboratories Inc. in the United States, and UL94 is also a flame retardant standard. After the evaluations, flammability (UL94V) grades were judged according to the defined judgement criteria.
  • Flammability has three stages of judgement criteria, V-0, V-1, and V-2, and is ranked in an order of V-0>V-1>V-2, in which V-0 indicates the most excellent flame retardancy among the three grades.
  • V-0 was set to satisfy the V-0 judgement criteria for all 10 test pieces in total in the vertical and horizontal directions.
  • V-2 was set to satisfy the V-2 judgement criteria for at least one of all 10 test pieces in total in the vertical and horizontal directions.
  • a comprehensive evaluation of a fabric body obtained was performed according to the following criteria.
  • Constituent materials were dry-blended and melt-kneaded at a temperature setting of 240°C using a twin-screw extruder having a screw of 45 mm ⁇ , followed by discharged in a strand shape, and then pelletized to ⁇ 3 mm and a length of 3 mm using a pelletizer.
  • a method of producing a polyester elastomer will be described.
  • a polyester block copolymer (A1-1) containing, as constituent components, 80% by mass of a high-melting point crystalline segment (H1) having a crystalline aromatic polyester as a main structural unit and 20% by mass of a low-melting point polymer segment (L1) having an aliphatic polyether as a main structural unit was produced.
  • tetra-n-butyl titanate 0.15 parts was additionally added to the reaction mixture, 0.05 parts of "Irganox” 1098 (a hindered phenol-based antioxidant manufactured by Ciba-Geigy AG) was added, and then the temperature was raised to 245°C, and next, a pressure in the system was reduced to 27 Pa over 50 minutes to perform polymerization for 1 hour and 50 minutes under this condition. The resulting polymer was discharged into water in a strand shape and cut into a pellet. The melting point was 164°C.
  • a slurry of 1100 parts by mass of terephthalic acid and 480 parts by mass of ethylene glycol was supplied over 3 hours to an esterification reaction vessel charged with 1950 parts by mass of bishydroxyethyl terephthalate and maintained at a temperature of 245°C to perform an esterification reaction while distilling water out of the reaction system. 1300 parts by mass of a low polymer after the reaction was transferred to a polycondensation reaction vessel.
  • a predetermined torque of a stirrer When a predetermined torque of a stirrer is obtained, nitrogen is flowed into the reaction system to return the pressure to normal to stop the polymerization reaction, and the mixture was discharged in a strand shape from a lower part of a polymerization can, cooled and solidified, and then cut to obtain a pellet of a phosphorus atom-containing flame-retardant polyester composition.
  • the obtained phosphorus atom-containing polyester had an intrinsic viscosity of 0.75, a melting point of 239°C, and a content of phosphorus elemental of 0.67 wt%.
  • 101 parts of terephthalic acid, 50.0 parts of 1,4-butanediol, and 71.0 parts of poly(oxytetramethylene) glycol having a number average molecular weight of about 1400 were charged together with 0.06 parts of titanium tetrabutoxide and 0.04 parts of mono-n-butyl-monohydroxy tin oxide in a reaction vessel equipped with a helical ribbon type stirring blade and heated at 190 to 225°C for 3 hours to perform an esterification reaction while allowing reaction water to flow out of a system.
  • a slurry of 1100 parts by mass of terephthalic acid and 480 parts by mass of ethylene glycol was supplied over 3 hours to an esterification reaction vessel charged with 1950 parts by mass of bishydroxyethyl terephthalate and maintained at a temperature of 245°C to perform an esterification reaction while distilling water out of the reaction system. 1300 parts by mass of a low polymer after the reaction was transferred to a polycondensation reaction vessel.
  • a predetermined torque of a stirrer When a predetermined torque of a stirrer is obtained, nitrogen is flowed into the reaction system to return the pressure to normal to stop the polymerization reaction, and the mixture was discharged in a strand shape from a lower part of a polymerization can, cooled and solidified, and then cut to obtain a pellet of a phosphorus atom-containing flame-retardant polyester composition.
  • the obtained phosphorus atom-containing polyester had an intrinsic viscosity of 0.72, a melting point of 245°C, and a content of phosphorus elemental of 0.50 wt%.
  • a polyester elastomer (A1) and a flame retardant (B1) were kneaded to obtain a pellet (A1-B1) containing the flame retardant and the polyester elastomer.
  • a flame retardant B1
  • an organic phosphorus-containing compound "Fireguard” FCX-210 manufactured by TEIJIN LIMITED was used as (B1).
  • the pellet (A1-B1) containing the flame retardant and the polyester elastomer was used as a polymer used for the core and a polyester (A3) was used as a polymer used for the sheath to be spun so as to achieve the ratios of the core and sheath as described in Table 1 to obtain a monofilament.
  • the monofilament was a core-sheath composite fiber, which had a 70% by volume of fraction of the core and a 30% by volume of fraction of the sheath.
  • spinnability filter clogging was rated as A, scum generation was rated as A, yarn breakage was rated as A, and the number of occurrences of bump yarn was rated as A and a comprehensive evaluation of spinnability was A.
  • a flame retardant contained in the sheath was a phosphorus compound 1 (2-carboxyethyl(phenyl)phosphinic acid), and a content of phosphorus element contained in the sheath was 0.7% by mass.
  • the obtained monofilament and a two-ply yarn of a false twisted polyester yarn of 167 dtex as another yarn were used to be knitted with a weft knitting machine so that a content of the monofilament to a fabric was 70% by mass.
  • the edge of the fabric was supported and attached by a metal frame member having an inner frame size of 500 mm ⁇ 500 mm to obtain a fabric body in which shrinkage is expressed in the fabric by dry heat treatment (185°C ⁇ 15 minutes).
  • Table 1 shows configurations and performances of this fabric body.
  • a fabric and a fabric body were produced and evaluated in the same manner as in Example 1, except that a ratio of a core and a sheath, a content of a flame retardant, and a content of phosphorus element were changed as shown in Table 1. The results are shown in Table 1.
  • Example 1 Regarding a flame retardant contained in a core, a fabric and a fabric body were produced and evaluated in the same manner as in Example 1, except that B2 as described below was added to the flame retardant of Example 1. The results are shown in Table 1.
  • HALS hindered amine-based light stabilizer
  • Example 1 Regarding a flame retardant contained in a core, a fabric and a fabric body were produced and evaluated in the same manner as in Example 1, except that the flame retardant in Example 1 was changed to B3 as described below. The results are shown in Table 1.
  • Example 1 Regarding a flame retardant contained in a core, a fabric and a fabric body were produced and evaluated in the same manner as in Example 1, except that the flame retardant in Example 1 was changed to B4 as described below. The results are shown in Table 1.
  • Example 1 Regarding a flame retardant contained in a sheath, a fabric and a fabric body were produced and evaluated in the same manner as in Example 1, except that the flame retardant in Example 1 was changed to B3 as described below. The results are shown in Table 1.
  • Example 2 a fabric and a fabric body were produced and evaluated in the same manner as in Example 1, except that the polymer in Example 1 was changed to a polyester elastomer (A1) and a polyester elastomer (A2) that were used in combination. The results are shown in Table 2.
  • Example 2 a fabric and a fabric body were produced and evaluated in the same manner as in Example 1, except that the polymer in Example 1 was changed to a polyester (A6) that contains no phosphorus element as a flame retardant. The results are shown in Table 2.
  • Example 7 a fabric and a fabric body were produced and evaluated in the same manner as in Example 1, except that the polymer in Example 1 was changed to a polyester (A7) that contains a copolymerized phosphorus compound 2.
  • the results are shown in Table 2.
  • the phosphorus compound 2 was (2-carboxyethyl)methylphosphinic acid, and a content of phosphorus element contained in a sheath was 0.5% by mass.
  • Example 2 a fabric and a fabric body were produced and evaluated in the same manner as in Example 1, except that the polymer in Example 1 was changed to a polyester elastomer (A4). The results are shown in Table 2.
  • Example 2 a fabric and a fabric body were produced and evaluated in the same manner as in Example 1, except that the polymer in Example 1 was changed to a polyester elastomer (A5). The results are shown in Table 2.
  • a fabric and a fabric body were produced and evaluated in the same manner as in Example 1, except that a ratio of a core and a sheath, a content of a flame retardant, and a content of phosphorus element were changed as shown in Table 2. The results are shown in Table 3.
  • Example 1 Example 2
  • Example 3 Example 4
  • Example 5 Example 6
  • Example 7 Monofilament Fiber form - Core-sheath composite Core-sheath composite Core-sheath composite Core-sheath composite Core-sheath composite Core-sheath composite Base polymer in core - Polyester elastomer (A1) Polyester elastomer (A1) Polyester elastomer (A1) Polyester elastomer (A1) Polyester elastomer (A1) Polyester elastomer (A1) Base polymer in sheath - Polyester (A3) Polyester (A3) Polyester (A3) Polyester (A3) Polyester (A3) Polyester (A3) Polyester (A3) Polyester (A3) Polyester (A3) Polyester (A3) Polyester (A3) Polyester (A3) Polyester (A3) Polyester (A3) Polyester (A3) Polyester (A3) Polyester (A3) Fraction of core % by volume 70 60 90 70 70 70 70 Fraction of sheath % by volume 30 40 10 30 30 30 30 30 30 30 30 30 30 Flame retardant contained in core 1.
  • Organic phosphate 1 Organic phosphate 1. Organic phosphate 1. Organic phosphate 1. Organic phosphate 1. Organic phosphate 1. Organic phosphate Content of flame retardant contained in core % by mass 20 20 20 20 20 20 Flame retardant contained in sheath - Phosphorus compound 1 - Phosphorus compound 2 Phosphorus compound 1 Phosphorus compound 1 Content of phosphorus element based on entire sheath % by mass 0.7 - 0.5 0.7 0.7 Total fineness dtex 760 760 760 760 760 760 760 Dry heat shrinkage % 24.5 20.0 23.0 26.0 30.0 Spinnability Filter clogging - A A A A A A Scum generation - A A A A A A Unit Example 15 Example 16 Example 17 Example 18 Example 19 Yarn breakage - A A A A A A Number of occurrences of bump yarn - A A A A A A A A A A A A A Other yarn (multifilament) - False-twisted PET (167T/2-48) False-twisted PET
  • Organic phosphate 1. Organic phosphate 1. Organic phosphate 1. Organic phosphate 1. Organic phosphate Content of flame retardant contained in core % by mass 20 20 20 20 20 - 20 Flame retardant contained in sheath Phosphorus compound 1 Phosphorus compound 1 Phosphorus compound 1 Phosphorus compound 1 1.

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Manufacturing & Machinery (AREA)
  • Multicomponent Fibers (AREA)
  • Knitting Of Fabric (AREA)
  • Woven Fabrics (AREA)
EP22746003.7A 2021-01-29 2022-01-27 Fabric, fabric object, and sheet Pending EP4273312A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2021013376 2021-01-29
PCT/JP2022/003188 WO2022163784A1 (ja) 2021-01-29 2022-01-27 布帛、布帛体およびシート

Publications (1)

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EP4273312A1 true EP4273312A1 (en) 2023-11-08

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EP (1) EP4273312A1 (ja)
JP (1) JP2022117482A (ja)
KR (1) KR20230137873A (ja)
CN (1) CN116745476A (ja)
WO (1) WO2022163784A1 (ja)

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH03279429A (ja) * 1990-03-27 1991-12-10 Toray Ind Inc 複合繊維
JPH11222729A (ja) * 1998-02-04 1999-08-17 Toyobo Co Ltd 難燃性に優れた弾性複合フィラメント
JP4431906B2 (ja) * 1999-02-26 2010-03-17 東洋紡績株式会社 インテリア用伸縮性編地、その製造方法及びシート成形方法
JP2001303395A (ja) * 2000-04-27 2001-10-31 Toyobo Co Ltd 弾性織編物及びその製造方法
JP2011021287A (ja) * 2009-07-15 2011-02-03 Teijin Fibers Ltd 深色性芯鞘型複合繊維
JP7305974B2 (ja) 2018-02-22 2023-07-11 東レ株式会社 布帛体の製造方法

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KR20230137873A (ko) 2023-10-05
CN116745476A (zh) 2023-09-12
WO2022163784A1 (ja) 2022-08-04

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