WO2021176831A1 - 人工毛髪用芯鞘複合繊維、それを含む頭飾製品及びその製造方法 - Google Patents

人工毛髪用芯鞘複合繊維、それを含む頭飾製品及びその製造方法 Download PDF

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Publication number
WO2021176831A1
WO2021176831A1 PCT/JP2021/000050 JP2021000050W WO2021176831A1 WO 2021176831 A1 WO2021176831 A1 WO 2021176831A1 JP 2021000050 W JP2021000050 W JP 2021000050W WO 2021176831 A1 WO2021176831 A1 WO 2021176831A1
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WIPO (PCT)
Prior art keywords
core
sheath
fiber
artificial hair
composite fiber
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.)
Ceased
Application number
PCT/JP2021/000050
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English (en)
French (fr)
Japanese (ja)
Inventor
荻野貴志
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Kaneka Corp
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Kaneka Corp
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Publication date
Application filed by Kaneka Corp filed Critical Kaneka Corp
Priority to JP2022504998A priority Critical patent/JPWO2021176831A1/ja
Publication of WO2021176831A1 publication Critical patent/WO2021176831A1/ja
Priority to US17/881,897 priority patent/US20220372669A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • A—HUMAN NECESSITIES
    • A41—WEARING APPAREL
    • A41G—ARTIFICIAL FLOWERS; WIGS; MASKS; FEATHERS
    • A41G3/00—Wigs
    • A—HUMAN NECESSITIES
    • A41—WEARING APPAREL
    • A41G—ARTIFICIAL FLOWERS; WIGS; MASKS; FEATHERS
    • A41G5/00—Hair pieces, inserts, rolls, pads, or the like; Toupées
    • A41G5/004—Hair pieces
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/001—Combinations of extrusion moulding with other shaping operations
    • B29C48/0022—Combinations of extrusion moulding with other shaping operations combined with cutting
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/022—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the choice of material
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/03—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
    • B29C48/05—Filamentary, e.g. strands
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/16—Articles comprising two or more components, e.g. co-extruded layers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/16—Articles comprising two or more components, e.g. co-extruded layers
    • B29C48/18—Articles comprising two or more components, e.g. co-extruded layers the components being layers
    • B29C48/21—Articles comprising two or more components, e.g. co-extruded layers the components being layers the layers being joined at their surfaces
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/25—Component parts, details or accessories; Auxiliary operations
    • B29C48/30—Extrusion nozzles or dies
    • B29C48/345—Extrusion nozzles comprising two or more adjacently arranged ports, for simultaneously extruding multiple strands, e.g. for pelletising
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
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    • B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/25—Component parts, details or accessories; Auxiliary operations
    • B29C48/36—Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die
    • B29C48/365—Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die using pumps, e.g. piston pumps
    • B29C48/37—Gear pumps
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/25—Component parts, details or accessories; Auxiliary operations
    • B29C48/36—Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die
    • B29C48/375—Plasticisers, homogenisers or feeders comprising two or more stages
    • B29C48/387—Plasticisers, homogenisers or feeders comprising two or more stages using a screw extruder and a gear pump
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/25—Component parts, details or accessories; Auxiliary operations
    • B29C48/36—Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die
    • B29C48/395—Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die using screws surrounded by a cooperating barrel, e.g. single screw extruders
    • B29C48/40—Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die using screws surrounded by a cooperating barrel, e.g. single screw extruders using two or more parallel screws or at least two parallel non-intermeshing screws, e.g. twin screw extruders
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
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    • B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/25—Component parts, details or accessories; Auxiliary operations
    • B29C48/78—Thermal treatment of the extrusion moulding material or of preformed parts or layers, e.g. by heating or cooling
    • B29C48/80—Thermal treatment of the extrusion moulding material or of preformed parts or layers, e.g. by heating or cooling at the plasticising zone, e.g. by heating cylinders
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/25—Component parts, details or accessories; Auxiliary operations
    • B29C48/78—Thermal treatment of the extrusion moulding material or of preformed parts or layers, e.g. by heating or cooling
    • B29C48/86—Thermal treatment of the extrusion moulding material or of preformed parts or layers, e.g. by heating or cooling at the nozzle zone
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/25—Component parts, details or accessories; Auxiliary operations
    • B29C48/78—Thermal treatment of the extrusion moulding material or of preformed parts or layers, e.g. by heating or cooling
    • B29C48/86—Thermal treatment of the extrusion moulding material or of preformed parts or layers, e.g. by heating or cooling at the nozzle zone
    • B29C48/872—Thermal treatment of the extrusion moulding material or of preformed parts or layers, e.g. by heating or cooling at the nozzle zone characterised by differential heating or cooling
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D5/00—Formation of filaments, threads, or the like
    • D01D5/08—Melt spinning methods
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D5/00—Formation of filaments, threads, or the like
    • D01D5/253—Formation of filaments, threads, or the like with a non-circular cross section; Spinnerette packs therefor
    • D—TEXTILES; PAPER
    • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
    • D01D5/00—Formation of filaments, threads, or the like
    • D01D5/28—Formation of filaments, threads, or the like while mixing different spinning solutions or melts during the spinning operation; Spinnerette packs therefor
    • D01D5/30—Conjugate filaments; Spinnerette packs therefor
    • D01D5/34—Core-skin structure; Spinnerette packs therefor
    • 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
    • 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
    • D01F8/12—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers with at least one polyamide as constituent
    • 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
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C2948/00—Indexing scheme relating to extrusion moulding
    • B29C2948/92—Measuring, controlling or regulating
    • B29C2948/92504—Controlled parameter
    • B29C2948/92704—Temperature
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2067/00—Use of polyesters or derivatives thereof, as moulding material
    • B29K2067/003—PET, i.e. poylethylene terephthalate
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2077/00—Use of PA, i.e. polyamides, e.g. polyesteramides or derivatives thereof, as moulding material
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
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    • B29K2995/00—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
    • B29K2995/0012—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds having particular thermal properties
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Definitions

  • the present invention relates to a core-sheath composite fiber for artificial hair that can be used as a substitute for human hair, a headdress product containing the same, and a method for producing the same.
  • Human hair has traditionally been used in headdress products such as wigs, hair wigs, hair attachments, hair bands, and doll hair.
  • headdress products such as wigs, hair wigs, hair attachments, hair bands, and doll hair.
  • synthetic fibers used for artificial hair include acrylic fibers, vinyl chloride fibers, vinylidene chloride fibers, polyester fibers, polyamide fibers, and polyolefin fibers.
  • Artificial hair is required to have a feel and appearance similar to human hair.
  • Patent Document 2 As a technique for bringing the tactile sensation of artificial hair fibers closer to the tactile sensation of human hair, as in Patent Document 2, a polyamide-based component having a highly rigid polyester fiber as a core and surrounding the core to obtain a tactile sensation very close to that of human hair. A composite spinning technique with improved tactile sensation has been proposed by coating with.
  • Patent Document 1 has a problem that it is necessary to combine a plurality of fibers having different fineness by post-processing, and the processing man-hours increase. Further, the problem that can be solved by the technique described in Patent Document 1 is specialized in texture, and cannot be solved in terms of tactile sensation. On the other hand, the fibers described in Patent Document 2 have a good tactile sensation, but have a problem that the gloss has glare peculiar to synthetic fibers and is far from human hair.
  • the present invention provides a core-sheath composite fiber for artificial hair having a tactile sensation close to that of human hair and having good gloss, a headdress product containing the same, and a method for producing the same.
  • the present invention is, in one or more embodiments, a core-sheath composite fiber for artificial hair including a core portion and a sheath portion, wherein the core portion is composed of a polyester-based resin composition containing a polyester-based resin, and the sheath portion.
  • the core portion is composed of a polyester-based resin composition containing a polyester-based resin
  • the sheath portion is composed of a polyamide-based resin composition containing a polyamide-based resin
  • the core-sheath composite fiber for artificial hair has a single fiber fineness of 20 dtex or more and 80 dtex or less, and a fluctuation coefficient of the fiber warp of the single fiber is 10%.
  • the present invention relates to a core-sheath composite fiber for artificial hair, which is characterized by being 40% or more and 40% or less.
  • the present invention also relates to a headdress product comprising the core-sheath composite fiber for artificial hair in one or more embodiments.
  • the present invention is also a method for producing a core-sheath composite fiber for artificial hair according to one or more embodiments, wherein a polyester-based resin composition and a polyamide-based resin composition are melt-spun using a core-sheath type composite nozzle.
  • the polyamide-based resin composition comprises a core-sheath composite fiber for artificial hair, wherein the melt viscosity at a set temperature of the core-sheath type composite nozzle is in the range of 200 Pa ⁇ s or more and 250 Pa ⁇ s or less. Regarding the manufacturing method of.
  • a core-sheath composite fiber for artificial hair and a headdress product having a tactile sensation close to that of human hair and having a natural luster like human hair.
  • a core-sheath composite fiber for artificial hair having a tactile sensation close to that of human hair and having a natural luster like human hair.
  • FIG. 1 is a schematic view showing a fiber cross section of a core-sheath composite fiber for artificial hair according to an example of the present invention.
  • the present inventor has made extensive studies to solve the above problems.
  • the core is composed of the polyester-based resin composition containing the polyester-based resin
  • the sheath is formed of the polyamide-based resin composition containing the polyamide-based resin.
  • the core-sheath composite fiber for artificial hair has a single fiber fineness of 20 dtex or more and 80 dtex or less. As a result, artificial hair fibers having a tactile sensation and gloss similar to those of human hair can be obtained.
  • the core-sheath composite fiber for artificial hair preferably has a single fiber fineness of 30 dtex or more and 70 dtex or less, and more preferably 40 dtex or more and 60 dtex or less.
  • the single fiber fineness of the core-sheath composite fiber for artificial hair can be obtained, for example, by measuring the fineness of 10 samples (single fibers) using a fineness measuring device and calculating the average value thereof.
  • the coefficient of variation (CV value) of the fiber warp of a single fiber of the core-sheath composite fiber for artificial hair is 10% or more and 40% or less.
  • CV value of the fiber diameter of the single fiber is less than 10%, the undulations of the fiber surface are small and the surface becomes smooth, so that the scattering of incident light becomes insufficient, and the glaring luster peculiar to the synthetic fiber is obtained. The feel is also flat.
  • the CV value of the fiber diameter of the single fiber is larger than 40%, the undulations on the fiber surface become large, so that the glare gloss is suppressed, but the tactile sensation is greatly deteriorated.
  • the coefficient of variation (CV value) of the fiber warp of the single fiber is, for example, 10 single fibers selected arbitrarily as a sample, and the fiber length of each single fiber is measured by a fineness measuring device.
  • the fiber diameters of 10 points are measured every 10 cm in the direction, and the calculation is performed by the following formula (1) based on the data of the fiber diameters of a total of 100 points.
  • the cross-sectional shape of the core-sheath composite fiber for artificial hair is not particularly limited, and may be circular or irregular. Examples of the variant include a multi-leaf shape such as an elliptical shape and a flat bilobed shape.
  • the cross-sectional shape of the core-sheath composite fiber for artificial hair and the cross-sectional shape of the core portion may be the same or different. From the viewpoint of tactile sensation, gloss, combability, etc., the core portion is a deformed flat bilobed shape or a deformed elliptical shape having a pair of convex portions protruding from the center side toward the outer peripheral side along the minor axis direction of the fiber cross section. It preferably has a cross-sectional shape.
  • the flat bilobed shape is a combination of two leaf shapes selected from the group consisting of a round shape and an elliptical shape via a recess. Further, the circular or elliptical shape does not necessarily have to draw a continuous arc, and includes a substantially circular or substantially elliptical shape in which a part is deformed unless the angle is acute.
  • FIG. 1 is a schematic view showing a fiber cross section of a core-sheath composite fiber for artificial hair according to an example of the present invention.
  • the core-sheath composite fiber 1 for artificial hair is composed of a sheath portion 10 and a core portion 20, and both the fiber 1 and the core portion 20 have a flat bilobed fiber cross section in which two elliptical shapes are connected via recesses. Have.
  • the straight line that is the longest of the straight lines connecting arbitrary two points on the outer circumference of the fiber cross section so as to be parallel to the line symmetry axis and the line symmetry axis.
  • L the length of a certain fiber cross-section long axis
  • S1 the length of the short axis of the fiber cross section, which is a straight line connecting the points, satisfies the following formula (2).
  • the core cross section length is the maximum straight line connecting arbitrary two points on the outer periphery of the core cross section so as to be parallel to the line symmetry axis and the line symmetry axis.
  • Lc length when the length of the shaft
  • Sc1 the length of the short axis of the cross section of the core portion, which is a straight line to be connected
  • the deformed flat bilobed shape is a deformed flat bilobed shape, and is a flat bilobed shape having a pair of convex portions protruding from the central side toward the outer peripheral side along the minor axis direction of the fiber cross section.
  • two leaf shapes selected from the group consisting of circular and elliptical shapes are connected via a concave portion, whereas two leaf shapes selected from the group consisting of circular and elliptical shapes are convex parts. It is connected via.
  • the cross-sectional shape of the fiber and core and the core-sheath ratio described above can be controlled by using a nozzle (hole) having a shape close to the target cross-sectional shape.
  • the core-sheath ratio of the core-sheath composite fiber for artificial hair is preferably in the range of 2: 8 to 8: 2 in terms of area ratio of core: sheath. If the core-sheath ratio is out of this range and the ratio of any of the components is small, the discharge of the component with a small ratio is difficult to stabilize and large irregularities are likely to be formed, so that the coefficient of variation of the fiber warp of the single fiber becomes large. It is easy and the gloss may be reduced. Further, when the core-sheath ratio is in this range, the bending rigidity value as a physical property related to the tactile sensation and texture becomes close to that of human hair, so that artificial hair of the same quality as human hair can be easily obtained.
  • the core-sheath ratio of the core-sheath composite fiber for artificial hair is more preferably in the range of 3: 7 to 7: 3 in terms of area ratio.
  • the core-sheath composite fiber for artificial hair does not necessarily have to have the same fineness and cross-sectional shape, and fibers having different fineness and cross-sectional shape may be mixed. Further, in the fiber cross section of the core-sheath composite fiber for artificial hair, in order to prevent the core and the sheath from peeling off, it is preferable that the core is not exposed on the fiber surface and is completely covered by the sheath. ..
  • the core portion is composed of a polyester-based resin composition containing a polyester-based resin, that is, a polyester-based resin composition containing a polyester-based resin as a main component
  • the sheath portion is a polyamide containing a polyamide-based resin. It is composed of a based resin composition, that is, a polyamide resin composition containing a polyamide resin as a main component.
  • the polyamide-based resin composition containing a polyamide-based resin as a main component means that the polyamide-based resin is contained in an amount of more than 50% by weight when the total weight of the polyamide-based resin composition is 100% by weight. Is preferably contained in an amount of 70% by weight or more, more preferably 80% by weight or more, further preferably 90% by weight or more, and further preferably 95% by weight or more.
  • the polyester-based resin composition containing a polyester-based resin as a main component means that the polyester-based resin is contained in an amount of more than 50% by weight when the total weight of the polyester-based resin composition is 100% by weight. Is preferably contained in an amount of 70% by weight or more, more preferably 80% by weight or more, further preferably 90% by weight or more, and further preferably 95% by weight or more.
  • a flame retardant can be used in combination, and a polyester resin composition containing a polyester resin and a bromine polymer flame retardant, or a polyamide containing a polyamide resin and a bromine polymer flame retardant.
  • a based resin composition or the like is preferably used.
  • the core-sheath composite fiber for artificial hair is composed of a polyester-based resin composition containing a polyester-based resin and a bromine-based polymer flame retardant, and a polyamide-based sheath. It is preferably composed of a polyester resin composition containing a resin and a brominated polymer flame retardant.
  • the polyalkylene terephthalate is not particularly limited, and examples thereof include polyethylene terephthalate, polypropylene terephthalate, polybutylene terephthalate, and polycyclohexanedimethylene terephthalate.
  • the copolymerized polyester mainly composed of the above polyalkylene terephthalate is not particularly limited, but for example, it is mainly composed of polyalkylene terephthalate such as polyethylene terephthalate, polypropylene terephthalate, polybutylene terephthalate, and polycyclohexanedimethylene terephthalate, and other copolymerization components. Examples thereof include copolymerized polyester containing.
  • "Copolymerized polyester mainly containing polyalkylene terephthalate” refers to a copolymerized polyester containing 80 mol% or more of polyalkylene terephthalate.
  • copolymerization components include, for example, isophthalic acid, orthophthalic acid, naphthalenedicarboxylic acid, paraphenylenedicarboxylic acid, trimellitic acid, pyromellitic acid, succinic acid, glutaric acid, adipic acid, suberic acid, azelaic acid, sebacic acid.
  • Polyvalent carboxylic acids such as dodecanedioic acid and their derivatives; dicarboxylic acids including sulfonates such as 5-sodium sulfoisophthalic acid, 5-sodium sulfoisophthalate dihydroxyethyl and their derivatives; 1,2-propanediol , 1,3-Propanediol, 1,4-Butanediol, 1,6-Hexanediol, Neopentylglycol, 1,4-Cyclohexanedimethanol, Diethyleneglycol, Polyethylene glycol, Trimethylolpropane, Pentaerythritol, 4-Hydroxybenzo Examples thereof include acid, ⁇ -caprolactone, and ethylene glycol ether of bisphenol A.
  • the copolymerized polyester is preferably produced by reacting the main polyalkylene terephthalate with a small amount of other copolymerizing components.
  • the polyalkylene terephthalate a polymer of terephthalic acid and / or a derivative thereof (for example, methyl terephthalate) and alkylene glycol can be used.
  • the copolymerized polyester is a mixture of terephthalic acid and / or a derivative thereof (for example, methyl terephthalate) used for the polymerization of the main polyalkylene terephthalate and alkylene glycol, and a small amount of other copolymerization components such as a monomer or an oligomer. It may be produced by polymerizing the one containing the component.
  • the copolymerized polyester may have the above-mentioned other copolymerization components polycondensed on the main chain and / or side chain of the main polyalkylene terephthalate, and the copolymerization method is not particularly limited.
  • copolymerized polyester mainly composed of polyalkylene terephthalate include, for example, ethylene glycol ether of bisphenol A, 1,4-cyclohexadimethanol, isophthalic acid and dihydroxyethyl 5-sodium sulfoisophthalate mainly composed of polyethylene terephthalate.
  • the copolymerized polyester mainly composed of polyalkylene terephthalate and polyalkylene terephthalate may be used alone or in combination of two or more.
  • polyester mainly composed of terephthalate and copolymerized with isophthalic acid and polyester mainly composed of polyethylene terephthalate and copolymerized with dihydroxyethyl 5-sodium sulfoisophthalate alone or in combination of two or more.
  • the melt viscosity of the polyester resin composition is preferably in the range of 250 Pa ⁇ s or more and 350 Pa ⁇ s or less under the set temperature of the nozzle, and more preferably 280 Pa ⁇ s or more and 320 Pa ⁇ s or less.
  • the melt viscosity is 250 Pa ⁇ s or more, the mechanical strength of the obtained fiber does not decrease and there is no risk of drip during the combustion test.
  • the melt viscosity is 350 Pa ⁇ s or less, the molecular weight does not increase too much, and melt spinning becomes easy.
  • the brominated polymer flame retardant is not particularly limited, but for example, it is preferable to use a brominated epoxy flame retardant from the viewpoint of heat resistance and flame retardancy.
  • a brominated epoxy flame retardant whose molecular end is composed of an epoxy group or tribromophenol can be used as a raw material, but the structure of the brominated epoxy flame retardant after melt-kneading is particularly high.
  • the total number of the constituent units represented by the following formula (1) and the constituent units in which at least a part of the following formula (1) is modified is 100 mol%, 80 mol% or more is represented by the following formula (1). It is preferably a constituent unit.
  • the structure of the brominated epoxy flame retardant may change at the molecular end after melt-kneading.
  • the molecular end of the brominated epoxy flame retardant may be substituted with an epoxy group or a hydroxyl group other than tribromophenol, a phosphoric acid group, a phosphonic acid group, or the like, and the molecular end is bonded to the polyester component by an ester group. You may.
  • a part of the structure other than the molecular terminal of the brominated epoxy flame retardant may be changed.
  • the secondary hydroxyl group of the brominated epoxy flame retardant and the epoxy group may be bonded to form a branched structure, and if the bromine content in the brominated epoxy flame retardant molecule does not change significantly, the formula (1) ) May be desorbed or added.
  • a polymer type brominated epoxy flame retardant as shown in the following formula (2) is preferably used.
  • m is 1 to 1000.
  • examples of the polymer-type brominated epoxy flame retardant shown in the following formula (2) include brominated epoxy flame retardants manufactured by Sakamoto Yakuhin Kogyo Co., Ltd. (trade name "SR-T2MP"). Commercially available products may be used.
  • the polyamide resin is nylon obtained by polymerizing one or more selected from the group consisting of lactam, a mixture of aminocarboxylic acid, dicarboxylic acid and diamine, a mixture of dicarboxylic acid derivative and diamine, and a salt of dicarboxylic acid and diamine. Means resin.
  • lactam examples include, but are not limited to, 2-azetidineone, 2-pyrrolidinone, ⁇ -valerolactam, ⁇ -caprolactam, enantractam, caprilactam, undecalactam, laurolactam and the like. .. Of these, ⁇ -caprolactam, undecalactam, and laurolactam are preferable, and ⁇ -caprolactam is particularly preferable. These lactams may be used alone or in a mixture of two or more.
  • aminocarboxylic acid examples are not particularly limited, but for example, 6-aminocaproic acid, 7-aminoheptanoic acid, 8-aminooctanoic acid, 9-aminononanoic acid, 10-aminodecanoic acid, 11-aminoundecanoic acid, 12 -Aminododecanoic acid and the like can be mentioned. Of these, 6-aminocaproic acid, 11-aminoundecanoic acid, and 12-aminododecanoic acid are preferable, and 6-aminocaproic acid is particularly preferable. These aminocarboxylic acids may be used alone or in a mixture of two or more.
  • dicarboxylic acid used in a mixture of dicarboxylic acid and diamine, a mixture of dicarboxylic acid derivative and diamine, or a salt of dicarboxylic acid and diamine are not particularly limited, but for example, oxalic acid, malonic acid, succinic acid, and glutal.
  • Acids adipic acids, pimelliic acids, suberic acids, azelaic acids, sebacic acids, undecanedioic acids, dodecanedioic acids, brushphosphoric acids, tetradecanedioic acids, pentadecanedioic acids, octadecanedioic acids and other aliphatic dicarboxylic acids, cyclohexanedicarboxylic acids, etc.
  • aromatic dicarboxylic acids such as alicyclic dicarboxylic acid, phthalic acid, isophthalic acid, terephthalic acid, and naphthalenedicarboxylic acid.
  • adipic acid, sebacic acid, dodecanedioic acid, terephthalic acid, and isophthalic acid are preferable, and adipic acid, terephthalic acid, and isophthalic acid are particularly preferable.
  • These dicarboxylic acids may be used alone or in a mixture of two or more.
  • diamine used in the mixture of dicarboxylic acid and diamine, the mixture of dicarboxylic acid derivative and diamine, or the salt of dicarboxylic acid and diamine are not particularly limited, but for example, 1,4-diaminobutane, 1,5-.
  • Diaminopentane 1,6-diaminohexane, 2-methyl-1,5-diaminopentane (MDP), 1,7-diaminoheptane, 1,8-diaminooctane, 1,9-diaminononane, 1,10-diaminodecane , 1,11-diaminoundecane, 1,12-diaminododecane, 1,13-diaminotridecane, 1,14-diaminotetradecane, 1,15-diaminopentadecane, 1,16-diaminohexadecan, 1,17-diaminohepta Diamines such as decane, 1,18-diaminooctadecane, 1,19-diaminononadecan, 1,20-diaminoeicosane, cyclohexanediamine, alicyclic diamines such as bis- (4-amin
  • Examples thereof include aromatic diamines such as -xylylene diamine and p-xylylene diamine. Of these, aliphatic diamines are particularly preferable, and hexamethylenediamine is particularly preferably used. These diamines may be used alone or in a mixture of two or more.
  • the polyamide resin (sometimes referred to as nylon resin) is not particularly limited, but for example, nylon 6, nylon 66, nylon 11, nylon 12, nylon 6/10, nylon 6/12, nylon 6T and / or 6I. It is preferable to use semi-aromatic nylon containing a unit, a copolymer of these nylon resins, and the like. In particular, a copolymer of nylon 6, nylon 66, nylon 6 and nylon 66 is more preferable.
  • the polyamide-based resin can be produced, for example, by a polyamide-based resin polymerization method in which a polyamide-based resin raw material is heated in the presence or absence of a catalyst. Stirring may or may not occur during the polymerization, but stirring is preferred to obtain a homogeneous product.
  • the polymerization temperature can be arbitrarily set according to the degree of polymerization, reaction yield, and reaction time of the target prepolymer, but a low temperature is preferable in consideration of the quality of the finally obtained polyamide resin.
  • the reaction rate can also be set arbitrarily. Although there is no limitation on the pressure, it is preferable to reduce the pressure inside the system in order to efficiently extract the volatile components to the outside of the system.
  • the end of the polyamide resin may be closed with a carboxylic acid compound or an amine compound as necessary as a terminal blocking agent.
  • a carboxylic acid compound or an amine compound as necessary as a terminal blocking agent.
  • the concentration of the terminal amino group or the terminal carboxyl group of the obtained nylon resin is lower than that when the terminal blocking agent is not used.
  • the terminal is closed with a dicarboxylic acid or diamine, the sum of the concentrations of the terminal amino group and the terminal carboxyl group does not change, but the ratio of the concentrations of the terminal amino group and the terminal carboxyl group changes.
  • carboxylic acid compound examples are not particularly limited, but for example, acetic acid, propionic acid, butyric acid, valeric acid, caproic acid, enanthic acid, capric acid, pelargonic acid, undecanoic acid, lauric acid, tridecanoic acid, myristic acid,
  • Alipid monocarboxylic acids such as myristoleic acid, palmitic acid, stearic acid, oleic acid, linoleic acid, and araquinic acid, alicyclic monocarboxylic acids such as cyclohexanecarboxylic acid and methylcyclohexanecarboxylic acid, benzoic acid, toluic acid, ethyl
  • Aromatic monocarboxylic acids such as benzoic acid and phenylacetic acid, oxalic acid, malonic acid, succinic acid, glutaric acid, adipic acid, pimelli acid, suberic acid, azelaic acid, sebac
  • amine compound examples are not particularly limited, but for example, butylamine, pentylamine, hexylamine, heptylamine, octylamine, 2-ethylhexylamine, nonylamine, decylamine, undecylamine, dodecylamine, tridecylamine, tetra.
  • Aliper monoamines such as decylamine, pentadecylamine, hexadecylamine, octadecylamine, nonadecilamine, and icosylamine, alicyclic monoamines such as cyclohexylamine and methylcyclohexylamine, aromatic monoamines such as benzylamine and ⁇ -phenylethylamine, 1 , 4-Diaminobutane, 1,5-diaminopentane, 1,6-diaminohexane, 1,7-diaminoheptane, 1,8-diaminooctane, 1,9-diaminononane, 1,10-diaminodecane, 1,11 -Diaminoundecane, 1,12-diaminododecane, 1,13-diaminotridecane, 1,14-diaminotetradecane, 1,15-diaminopentadecan
  • terminal group concentration of the polyamide resin there is no particular limitation on the terminal group concentration of the polyamide resin, but when it is necessary to improve the dyeability for fiber applications or when designing a material suitable for alloying for resin applications, the higher the terminal amino group concentration is. preferable. On the contrary, when it is desired to suppress coloring and gelation under long-term aging conditions, it is preferable that the terminal amino group concentration is low. Furthermore, if you want to suppress lactam regeneration during remelting, yarn breakage during melt spinning due to oligomer formation, mold deposit during continuous injection molding, and die mark generation during continuous extrusion of film, both the terminal carboxyl group concentration and the terminal amino group concentration are both. Lower is preferable.
  • the terminal group concentration may be adjusted depending on the intended use, but both the terminal amino group concentration and the terminal carboxyl group concentration are preferably 1.0 ⁇ 10 -5 to 15.0 ⁇ 10 -5 eq / g, more preferably. It is 2.0 ⁇ 10 -5 to 12.0 ⁇ 10 -5 eq / g, particularly preferably 3.0 ⁇ 10 -5 to 11.0 ⁇ 10 -5 eq / g.
  • a method of adding the terminal sequestering agent a method of adding the terminal sequestering agent at the same time as a raw material such as caprolactam at the initial stage of polymerization, a method of adding the nylon resin during the polymerization, and a method of adding the nylon resin when passing it through a vertical stirring thin film evaporator in a molten state. Etc. are adopted.
  • the terminal sequestering agent may be added as it is, or may be dissolved in a small amount of solvent and added.
  • the melt viscosity of the polyamide resin composition is preferably in the range of 200 Pa ⁇ s or more and 250 Pa ⁇ s or less under the nozzle set temperature. If the melt viscosity is within the above range, leveling on the fiber surface, that is, smoothing of undulations formed on the resin surface, can be achieved while maintaining the mechanical strength of the obtained fiber until it is discharged from the nozzle and cooled and solidified. When it occurs moderately, the coefficient of variation of the fiber warp of the single fiber becomes an appropriate range, and it becomes easy to obtain a fiber having a good gloss and a tactile sensation.
  • melt viscosity of the polyamide-based resin composition When the melt viscosity of the polyamide-based resin composition is higher than 250 Pa ⁇ s, leveling of the fiber surface after nozzle ejection is less likely to occur, so that the fiber surface is cooled and solidified with large undulations, and the coefficient of variation of the fiber warp of the single fiber is large. Tends to increase and the tactile sensation tends to deteriorate.
  • melt viscosity of the polyamide resin composition is lower than 200 Pa ⁇ s, the fiber surface after nozzle ejection is excessively leveled before it is cooled and solidified, resulting in a flat surface without undulations, and the fiber warp of a single fiber. The coefficient of variation of is likely to be small, and there is a risk that both gloss and tactile sensation will deteriorate.
  • the melt viscosity of the polyester-based resin composition or the polyamide-based resin composition is such that the pellet-shaped resin composition is dehumidified and dried so that the water content is 1000 ppm or less, the sample amount of the resin composition is 20 g, and the piston speed is 200 mm /
  • the nozzle temperature at the time of spinning is measured as the set temperature under the conditions of min, the capillary length of 20 mm, and the capillary diameter of 1 mm.
  • the measuring device includes a capillary rheometer LCR7000 manufactured by Dynisco.
  • the core-sheath composite fiber for artificial hair is made from a copolymerized polyester mainly composed of polyalkylene terephthalate and polyalkylene terephthalate, from the viewpoint of making the tactile sensation and appearance closer to human hair and further improving curl and curl retention. It is preferable to use a polyester resin composition containing one or more polyester resins selected from the above group, and the sheath portion is a polyamide resin mainly composed of at least one selected from the group consisting of nylon 6 and nylon 66. It is more preferable to use a polyamide-based resin composition containing the above.
  • the "polyamide-based resin mainly composed of at least one selected from the group consisting of nylon 6 and nylon 66" means a polyamide-based resin containing 80 mol% or more of nylon 6 and / or nylon 66.
  • the core-sheath composite fiber for artificial hair includes flame retardants other than brominated epoxy flame retardants, flame retardants, heat resistant agents, stabilizers, fluorescent agents, as long as the effects of the present invention are not impaired. It may contain various additives such as antioxidants, antistatic agents and pigments.
  • Examples of flame retardants other than brominated epoxy flame retardants include phosphorus-containing flame retardants and bromine-containing flame retardants.
  • Examples of the phosphorus-containing flame retardant include a phosphate ester amide compound and an organic cyclic phosphorus-based compound.
  • Examples of the bromine-containing flame retardant include pentabromotoluene, hexabromobenzene, decabromodiphenyl, decabromodiphenyl ether, bis (tribromophenoxy) ethane, tetrabromobisphenol anhydride, ethylenebis (tetrabromophthalimide), and ethylenebis ().
  • Bromine-containing phosphate esters such as pentabromophenyl), octabromotrimethylphenyl indan, tris (tribromoneopentyl) phosphate; brominated polystyrenes; brominated polybenzyl acrylates; brominated phenoxy resins; brominated polycarbonate oligomers Tetrabromobisphenol A such as tetrabromobisphenol A, tetrabromobisphenol A-bis (2,3-dibromopropyl ether), tetrabromobisphenol A-bis (allyl ether), tetrabromobisphenol A-bis (hydroxyethyl ether) Derivatives; bromine-containing triazine-based compounds such as tris (tribromophenoxy) triazine; bromine-containing isocyanuric acid-based compounds such as tris (2,3-dibromopropyl) isocyanurate.
  • one or more selected from the group consisting of a phosphoric acid ester amide compound, an organic cyclic phosphorus-based compound, and a brominated phenoxy resin-based flame retardant is preferable because it has excellent flame retardancy.
  • Examples of the flame retardant aid include antimony compounds and composite metals containing antimony.
  • Examples of antimony compounds include antimony trioxide, antimony tetroxide, antimony pentoxide, sodium antimonate, potassium antimonate, calcium antimonate and the like. From the viewpoint of flame retardancy improving effect and influence on tactile sensation, one or more selected from the group consisting of antimony trioxide, antimony pentoxide, and sodium antimonate is more preferable.
  • the flame retardant aid is not particularly limited, but for example, it is preferable to include 0.1 part by weight or more and 10 parts by weight or less with respect to 100 parts by weight of the main component resin.
  • the core for artificial hair has a low-gloss appearance close to that of human hair.
  • Sheath composite fibers are easy to obtain.
  • the core-sheath composite fiber for artificial hair is melt-kneaded by using various general kneaders for each of the core resin composition and the sheath resin composition, and then melt-spun using a core-sheath type composite nozzle. It can be produced by.
  • a polyester-based resin composition obtained by dry-blending each component such as the above-mentioned polyester-based resin and brominated epoxy-based flame retardant is melt-kneaded using various general kneaders to obtain a core resin composition.
  • a polyamide resin composition in which each component such as the above-mentioned polyamide resin and brominated epoxy flame retardant is dry-blended is melt-kneaded using various general kneaders to obtain a sheath resin composition. It can be produced by melt spinning using a composite spinning nozzle.
  • the resin composition may contain other thermoplastic resins such as polycarbonate-based resins, if necessary.
  • the kneader include a single-screw extruder, a twin-screw extruder, a roll, a Banbury mixer, and a kneader. Of these, a twin-screw extruder is preferable from the viewpoint of adjusting the kneading degree and easiness of operation.
  • melt spinning for example, in the case of a polyester resin composition, the temperature of the extruder, gear pump, nozzle, etc. is 250 ° C. or higher and 300 ° C. or lower, and in the case of a polyamide resin composition, the temperature of the extruder, gear pump, nozzle, etc. The temperature is set to 260 ° C. or higher and 320 ° C. or lower, melt spinning is performed, the spun yarn is passed through a heating cylinder, and then cooled below the glass transition point of each resin at a speed of 50 m / min or more and 5000 m / min or less. By picking up, spun yarn (undrawn yarn) is obtained.
  • the core resin composition may be supplied by the core extruder, and the sheath resin composition may be supplied by the sheath extruder.
  • the spun yarn is heat-drawn.
  • the stretching may be carried out by either a two-step method in which the spun yarn is wound once and then stretched, or a direct spun drawing method in which the spun yarn is continuously stretched without being wound.
  • the thermal stretching is carried out by a one-step stretching method or a two-stage or more multi-step stretching method.
  • the fluctuation cycle of the sheath side nozzle pressure is 10 times / minute or more and 40 times / minute or less.
  • the coefficient of variation of the fiber warp of the single fiber tends to be 10% or more and 40% or less.
  • a heating roller As the heating means in the heat stretching, a heating roller, a heat plate, a steam jet device, a hot water tank, etc. can be used, and these can be used in combination as appropriate.
  • An oil agent such as a fiber treatment agent or a softener may be added to the core-sheath composite fiber for artificial hair to bring the texture and texture closer to human hair.
  • the fiber treatment agent include a silicone-based fiber treatment agent and a non-silicone-based fiber treatment agent for improving the tactile sensation and combability.
  • the core-sheath composite fiber for artificial hair may be processed by gear crimping.
  • gear crimping generally, fibers are passed between two meshed gears in a state of being heated to a softening temperature or higher, and the shape of the gears is transferred to develop fiber bending. Further, if necessary, curls of different shapes can be developed by heat-treating the core-sheath composite fibers for artificial hair at different temperatures in the fiber processing stage.
  • the core-sheath composite fiber for artificial hair can be used without particular limitation as long as it is a headdress product.
  • it can be used for hair wigs, wigs, weaving, hair extensions, blade hair, hair accessories, doll hair and the like.
  • the headdress product may be composed only of the core-sheath composite fiber for artificial hair of the present invention. Further, in the headdress product, the core-sheath composite fiber for artificial hair of the present invention may be combined with other fibers for artificial hair and natural fibers such as human hair and animal hair.
  • the measurement method and evaluation method used in the examples and comparative examples are as follows.
  • melt viscosity of polyamide resin composition The melt viscosity was measured with a resin viscometer (LCR7000 manufactured by Dynasco) using pellets of a polyamide-based resin composition dried to a water content of 1000 ppm or less. The measurement conditions were such that the cylinder temperature was the nozzle set temperature, that is, 260 ° C., the piston descent speed was 100 mm / min, and the die hole diameter was 1 mm. The sample amount was 20 g.
  • Example 1 Polyethylene terephthalate pellets dried to a water content of 100 ppm or less (manufactured by East West Chemical Private Limited, East PET product name "A-12", sometimes referred to as PET). 30 parts by weight of industrial product, trade name "SR-T2MP”) and 3 parts by weight of sodium antimonate (manufactured by Nippon Seiko Co., Ltd., product name "SA-A”) are added, and after dry blending, they are supplied to a twin shaft extruder. Melt kneading was carried out at a barrel set temperature of 280 ° C. and pelletization was performed to obtain a polyester resin composition. The pellet was dried again so that the water content was 100 ppm or less.
  • SR-T2MP trade name
  • SA-A sodium antimonate
  • nylon 6 manufactured by Unitika, trade name "A1030BRL", sometimes referred to as PA6
  • a brominated epoxy flame retardant manufactured by Sakamoto Yakuhin Kogyo, trade name
  • 12 parts by weight of "SR-T2MP” and 2 parts by weight of sodium antimonate manufactured by Nippon Seiko Co., Ltd., trade name "SA-A"
  • SA-A sodium antimonate
  • the pellet-shaped polyester-based resin composition and the polyamide-based resin composition are supplied to the extruder, respectively, and the nozzle setting temperature is 260 ° C., and a nozzle for concentric core-sheath type composite spinning (number of holes 120).
  • the polyester resin composition is used as the core
  • the polyamide resin composition is used as the sheath
  • the core-sheath ratio is the area ratio.
  • the obtained undrawn yarn was drawn using a heat roll at 85 ° C. at a speed of 45 m / min to obtain a triple drawn yarn, and further, 45 m / min using a heat roll continuously heated to 200 ° C. Take up and heat-treat at the speed of After adhering, it was dried to obtain a core-sheath composite fiber having a single fiber fineness of 80 dtex.
  • Example 2 Composite fibers were obtained in the same manner as in Example 1 except that the single fiber fineness was set to 50 dtex by adjusting the discharge amount.
  • Example 3 Composite fibers were obtained in the same manner as in Example 1 except that the single fiber fineness was set to 30 dtex by adjusting the discharge amount.
  • Example 4 Composite fibers were obtained in the same manner as in Example 1 except that the single fiber fineness was set to 20 dtex by adjusting the discharge amount.
  • Example 5 Composite fibers were obtained in the same manner as in Example 2 except that the core-sheath ratio was set to 8: 2.
  • Example 6 Composite fibers were obtained in the same manner as in Example 2 except that the core-sheath ratio was 2: 8.
  • Example 7 Composite fibers in the same manner as in Example 2 except that the temperature of the extruder for the sheath resin composition was changed so that the melt viscosity of the polyamide resin composition at the nozzle set temperature (260 ° C.) was 250 Pa ⁇ s. Got
  • Example 8 Composite fibers in the same manner as in Example 2 except that the temperature of the extruder for the sheath resin composition was changed so that the melt viscosity of the polyamide resin composition at the nozzle set temperature (260 ° C.) was 200 Pa ⁇ s. Got
  • Composite fibers were obtained in the same manner as in Example 1 except that the single fiber fineness was set to 90 dtex by adjusting the discharge amount.
  • Comparative Example 2 Composite fibers were obtained in the same manner as in Example 1 except that the single fiber fineness was set to 15 dtex by adjusting the discharge amount.
  • the fibers of Examples 1 to 8 have a single fiber fineness of 20 dtex or more and 80 dtex or less, and a CV value of the fiber warp of the single fiber is 10% or more and 40% or less, which is similar to human hair. It had a glossy and tactile sensation.
  • a core-sheath composite fiber for artificial hair including a core and a sheath.
  • the core portion is composed of a polyester resin composition containing a polyester resin
  • the sheath portion is composed of a polyamide resin composition containing a polyamide resin.
  • the core-sheath composite fiber for artificial hair is characterized in that the single fiber fineness is 20 dtex or more and 80 dtex or less, and the coefficient of variation of the fiber warp of the single fiber is 10% or more and 40% or less. fiber.
  • the polyester-based resin composition contains one or more polyester-based resins selected from the group consisting of polyalkylene terephthalate and copolymerized polyester mainly composed of polyalkylene terephthalate.
  • [5] The artificial hair according to any one of [1] to [4], wherein the polyamide-based resin composition contains a polyamide-based resin mainly composed of at least one selected from the group consisting of nylon 6 and nylon 66. Core sheath composite fiber.
  • [6] A headdress product comprising the core-sheath composite fiber for artificial hair according to any one of [1] to [5].
  • the method for producing a core-sheath composite fiber for artificial hair according to any one of [1] to [5]. Including a step of melt-spinning a polyester-based resin composition and a polyamide-based resin composition using a core-sheath type composite nozzle.
  • the polyamide-based resin composition is a method for producing a core-sheath composite fiber for artificial hair, wherein the melt viscosity of the core-sheath type composite nozzle at a set temperature is in the range of 200 Pa ⁇ s or more and 250 Pa ⁇ s or less.

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PCT/JP2021/000050 2020-03-03 2021-01-05 人工毛髪用芯鞘複合繊維、それを含む頭飾製品及びその製造方法 Ceased WO2021176831A1 (ja)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2023145171A1 (ja) * 2022-01-25 2023-08-03 デンカ株式会社 人工毛髪用繊維及び頭髪装飾製品

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004012542A1 (ja) * 2002-07-31 2004-02-12 Kaneka Corporation 人工毛髪用繊維及びその製造方法
WO2017187843A1 (ja) * 2016-04-28 2017-11-02 デンカ株式会社 人工毛髪繊維
WO2018179803A1 (ja) * 2017-03-30 2018-10-04 株式会社カネカ 人工毛髪用芯鞘複合繊維及びそれを含む頭飾製品

Family Cites Families (2)

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Publication number Priority date Publication date Assignee Title
JP2004012542A (ja) * 2002-06-03 2004-01-15 Canon Inc 現像剤規制部材、現像装置、プロセスカートリッジ及び画像形成装置
JP6597457B2 (ja) * 2016-04-01 2019-10-30 株式会社デンソー 運転支援装置

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004012542A1 (ja) * 2002-07-31 2004-02-12 Kaneka Corporation 人工毛髪用繊維及びその製造方法
WO2017187843A1 (ja) * 2016-04-28 2017-11-02 デンカ株式会社 人工毛髪繊維
WO2018179803A1 (ja) * 2017-03-30 2018-10-04 株式会社カネカ 人工毛髪用芯鞘複合繊維及びそれを含む頭飾製品

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2023145171A1 (ja) * 2022-01-25 2023-08-03 デンカ株式会社 人工毛髪用繊維及び頭髪装飾製品

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