US20080210250A1 - Fiber Bundle for Artificial Hair and Head Decoration Article Comprising the Same - Google Patents
Fiber Bundle for Artificial Hair and Head Decoration Article Comprising the Same Download PDFInfo
- Publication number
- US20080210250A1 US20080210250A1 US11/917,197 US91719706A US2008210250A1 US 20080210250 A1 US20080210250 A1 US 20080210250A1 US 91719706 A US91719706 A US 91719706A US 2008210250 A1 US2008210250 A1 US 2008210250A1
- Authority
- US
- United States
- Prior art keywords
- fibers
- vinyl chloride
- artificial hair
- fiber bundle
- shape
- 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.)
- Abandoned
Links
- 239000000835 fiber Substances 0.000 title claims abstract description 222
- 238000005034 decoration Methods 0.000 title claims description 12
- 238000000034 method Methods 0.000 claims abstract description 26
- 229920006312 vinyl chloride fiber Polymers 0.000 claims abstract description 15
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 66
- 229920005989 resin Polymers 0.000 claims description 46
- 239000011347 resin Substances 0.000 claims description 46
- 229920006026 co-polymeric resin Polymers 0.000 claims description 32
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 27
- 239000005977 Ethylene Substances 0.000 claims description 27
- 238000002074 melt spinning Methods 0.000 claims description 20
- 238000006116 polymerization reaction Methods 0.000 claims description 13
- 238000002156 mixing Methods 0.000 description 16
- 230000000052 comparative effect Effects 0.000 description 14
- 239000004014 plasticizer Substances 0.000 description 14
- 239000003017 thermal stabilizer Substances 0.000 description 13
- 239000000314 lubricant Substances 0.000 description 11
- 238000009987 spinning Methods 0.000 description 11
- 150000001875 compounds Chemical class 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 9
- 239000011342 resin composition Substances 0.000 description 9
- 229920001519 homopolymer Polymers 0.000 description 7
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 6
- 239000008188 pellet Substances 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 5
- 239000011295 pitch Substances 0.000 description 5
- 238000007669 thermal treatment Methods 0.000 description 5
- GDVKFRBCXAPAQJ-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O GDVKFRBCXAPAQJ-UHFFFAOYSA-A 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 229960001545 hydrotalcite Drugs 0.000 description 4
- 229910001701 hydrotalcite Inorganic materials 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 238000000465 moulding Methods 0.000 description 4
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- -1 polyethylene Polymers 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000000344 soap Substances 0.000 description 3
- 238000004383 yellowing Methods 0.000 description 3
- 239000004593 Epoxy Substances 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 229920001038 ethylene copolymer Polymers 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 235000012424 soybean oil Nutrition 0.000 description 2
- 239000003549 soybean oil Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000010557 suspension polymerization reaction Methods 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- QMMJWQMCMRUYTG-UHFFFAOYSA-N 1,2,4,5-tetrachloro-3-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl QMMJWQMCMRUYTG-UHFFFAOYSA-N 0.000 description 1
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- YLZOPXRUQYQQID-UHFFFAOYSA-N 3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]propan-1-one Chemical compound N1N=NC=2CN(CCC=21)CCC(=O)N1CCN(CC1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F YLZOPXRUQYQQID-UHFFFAOYSA-N 0.000 description 1
- DEXFNLNNUZKHNO-UHFFFAOYSA-N 6-[3-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperidin-1-yl]-3-oxopropyl]-3H-1,3-benzoxazol-2-one Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1CCN(CC1)C(CCC1=CC2=C(NC(O2)=O)C=C1)=O DEXFNLNNUZKHNO-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 240000008027 Akebia quinata Species 0.000 description 1
- 239000004604 Blowing Agent Substances 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- GWFGDXZQZYMSMJ-UHFFFAOYSA-N Octadecansaeure-heptadecylester Natural products CCCCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCCCC GWFGDXZQZYMSMJ-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- OCKWAZCWKSMKNC-UHFFFAOYSA-N [3-octadecanoyloxy-2,2-bis(octadecanoyloxymethyl)propyl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCCCCCCCC)(COC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC OCKWAZCWKSMKNC-UHFFFAOYSA-N 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- VBICKXHEKHSIBG-UHFFFAOYSA-N beta-monoglyceryl stearate Natural products CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- POULHZVOKOAJMA-UHFFFAOYSA-M dodecanoate Chemical compound CCCCCCCCCCCC([O-])=O POULHZVOKOAJMA-UHFFFAOYSA-M 0.000 description 1
- 238000000578 dry spinning Methods 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 229940070765 laurate Drugs 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- NKBWPOSQERPBFI-UHFFFAOYSA-N octadecyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCCCC NKBWPOSQERPBFI-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 230000002040 relaxant effect Effects 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 229940114926 stearate Drugs 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 238000002166 wet spinning Methods 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Images
Classifications
-
- 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
- D01F6/02—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D01F6/08—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polymers of halogenated hydrocarbons
- D01F6/10—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polymers of halogenated hydrocarbons from polyvinyl chloride or polyvinylidene chloride
-
- 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
- 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
- D01F6/28—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D01F6/32—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds comprising halogenated hydrocarbons as the major 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
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/44—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds as major constituent with other polymers or low-molecular-weight compounds
- D01F6/48—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds as major constituent with other polymers or low-molecular-weight compounds of polymers of halogenated hydrocarbons
-
- A—HUMAN NECESSITIES
- A41—WEARING APPAREL
- A41G—ARTIFICIAL FLOWERS; WIGS; MASKS; FEATHERS
- A41G3/00—Wigs
- A41G3/0083—Filaments for making wigs
Definitions
- the present invention relates to a fiber bundle of artificial hair to be used for hair decoration articles such as wigs, hairpieces, braided hair, extension hair, accessory hair or doll hair, and a head decoration article employing it.
- Units such as “parts” and “%” showing a blend composition of a resin composition will be represented by mass unless otherwise specified.
- Vinyl chloride resin fibers obtained by spinning a vinyl chloride resin are excellent in transparency and flexibility and thus are widely used as fibers for artificial hair to be used for head decoration articles such as wigs.
- a wet spinning method of spinning a vinyl chloride resin by using an organic solvent a dry spinning method or a melt spinning method of melt-spinning it without using an organic solvent, has been known.
- the melt spinning method is a method of extruding the resin at a high temperature under a high pressure by using an extruder.
- a vinyl chloride resin has a high melt viscosity and an extremely low spinning property, and thus, there has been a problem such that it is difficult to melt-spin the vinyl chloride resin to obtain vinyl chloride resin fibers having a prescribed quality.
- strands are extruded from nozzle holes having a small sectional area per hole, introduced into a heating cylinder and heat-melted and drawn therein to obtain unstretched fibers.
- they are discharged from nozzle holes having a small sectional area per hole, whereby there has been a problem that the pressure exerted to the nozzles tends to be high and is likely to exceed the pressure designed for the extruder, or there has been a problem such that gumming (scales around the nozzles) is likely to result.
- a means to incorporate a plasticizer and a vinyl chloride homopolymer having a low degree of polymerization has been proposed (e.g. Patent Document 1).
- fiber bundles for artificial hair processed by using the above-mentioned fibers for artificial hair are used as head decoration articles.
- Such fiber bundles for artificial hair are selected from those wherein the sectional shape of fibers is circular, oval, horseshoe, a cocoon-shape, a ribbon-shape or a star-shape, depending upon the properties such as the touch, the appearance, the gloss and the esthetic functionality attributable to human hair.
- the head decoration articles are generally classified into three styles of short, medium and long, and the required functions are different depending upon the styles. It has been common to modify the sectional shape of fibers to meet such requirements. However, with a single sectional shape, it has been impossible to meet the requirements of a wide range of hairstyles.
- Patent Document 2 In order to improve uniformity of curling to meet such requirements, a method to have a three-pronged sectional shape (e.g. Patent Document 2), a method to have a hollow section (e.g. Patent Document 3) or a method of mixing fibers having three types of sectional shapes (e.g. Patent Document 4) has been proposed.
- Patent Document 1 JP-A-11-61555
- Patent Document 2 JP-U-58-37961
- Patent Document 3 JP-U-63-48652
- Patent Document 4 JP-B-58-13641
- the present inventors have conducted an extensive study to accomplish the above object and as a result, have found that by mixing fibers having rigidities within certain ranges, a fiber bundle for artificial hair employing fibers for artificial hair made of vinyl chloride fibers, exhibits merits as a head decoration article effectively. Further, it has been found that as the above vinyl chloride fibers, fibers for artificial hair prepared under a low nozzle pressure with little gumming, are obtainable by melt-spinning a specific ethylene/vinyl chloride copolymer resin.
- the present invention has been made on the basis of the above discoveries and provides the following.
- a fiber bundle for artificial hair comprising fibers (A) having a flexural rigidity of (1.2 to 3.5) ⁇ 10 ⁇ 2 N cm 2 as determined by the KES method and fibers (B) having a flexural rigidity of (0.5 to 1.0) ⁇ 10 ⁇ 2 N cm 2 as determined by the KES method, wherein both of the fibers (A) and the fibers (B) are made of vinyl chloride fibers.
- the fiber bundle for artificial hair according to any one of the above (1) to (4), wherein the vinyl chloride fibers are made of fibers prepared by melt spinning an ethylene/vinyl chloride copolymer resin having an ethylene content of from 0.5 to 3 mass %.
- the present invention it is possible to easily obtain fibers for artificial hair prepared under a low nozzle pressure with little gumming, and it is further possible to obtain a fiber bundle for artificial hair having a soft touch close to human hair, while maintaining uniform curling.
- FIG. 1 is a schematic sectional view of a nozzle shape for fibers having a Y-shape cross section and the obtained fibers, representing one embodiment of the fiber bundle for artificial hair of the present invention.
- FIG. 2 is a is a schematic sectional view of a nozzle shape for fibers having a U-shape cross section and the obtained fibers, representing one embodiment of the fiber bundle for artificial hair of the present invention.
- FIG. 3 is a schematic sectional view of a nozzle shape for fibers having a C-shape cross section and the obtained fibers, representing one embodiment of the fiber bundle for artificial hair of the present invention.
- FIG. 4 is a schematic sectional view of a nozzle shape for fibers having a spectacled-shape cross section and the obtained fibers, representing one embodiment of the fiber bundle for artificial hair of the present invention.
- FIG. 5 is a schematic sectional view of a nozzle shape for fibers having an oval spectacled-shape cross section and the obtained fibers, representing one embodiment of the fiber bundle for artificial hair of the present invention.
- FIG. 6 is a schematic sectional view of a nozzle shape for fibers having a five leaf-shape cross section and the obtained fibers, representing one embodiment of the fiber bundle for artificial hair of the present invention.
- FIG. 7 is a schematic sectional view of a nozzle shape for fibers having a rod-shape cross section and the obtained fibers, representing one embodiment of the fiber bundle for artificial hair of the present invention.
- the fiber bundle for artificial hair of the present invention is composed of vinyl chloride fibers prepared by melt spinning a vinyl chloride resin.
- the vinyl chloride resin may be obtained by e.g. bulk polymerization, solution polymerization, suspension polymerization or emulsion polymerization. However, in consideration of e.g. the initial coloration of fibers, it is preferred to use ones prepared by suspension polymerization.
- the vinyl chloride resin may be a homopolymer resin which is a conventional homopolymer of vinyl chloride or various types of conventional copolymer resins and is not particularly limited.
- the copolymer resins are conventional copolymer resins including, for example, a copolymer resin of vinyl chloride with a vinyl ester, such as a vinyl chloride/vinyl acetate copolymer resin or a vinyl chloride/vinyl propionate copolymer resin, a copolymer resin of vinyl chloride with an acrylate, such as a vinyl chloride/butyl acrylate copolymer resin or a vinyl chloride/2-ethylhexyl acrylate copolymer resin, a copolymer resin of vinyl chloride with an olefin such as a vinyl chloride/ethylene copolymer resin or a vinyl chloride/propylene copolymer resin, and a vinyl chloride/acrylonitrile copolymer resin.
- a copolymer resin of vinyl chloride with a vinyl ester such as a vinyl chloride/vinyl acetate copolymer resin or a vinyl chloride/vinyl propionate cop
- a homopolymer resin which is a homopolymer of vinyl chloride, or a vinyl chloride/vinyl acetate copolymer resin.
- the content of the comonomer is not particularly limited and may be determined depending upon the required product quality such as the molding processability, fiber properties, etc.
- the vinyl chloride resin to be used in the present invention is preferably a homopolymer resin which is a homopolymer of vinyl chloride, a vinyl chloride/ethylene copolymer resin or a vinyl chloride/vinyl acetate copolymer resin.
- the content of the comonomer is not particularly limited and may be determined depending upon the required product quality such as the molding processability, fiber properties, etc.
- the viscosity average polymerization degree of the vinyl chloride resin is preferably from 600 to 2,500, more preferably from 900 to 2,500, particularly preferably from 1,000 to 2,000. If it is less than 600, the melt viscosity tends to be low, and the obtained fibers tend to be susceptible to thermal shrinkage. On the other hand, if it exceeds 2,500, the melt viscosity tends to be high, and the molding temperature of the fibers tends to be high, whereby coloration of fibers may sometimes result.
- the viscosity average polymerization degree is one calculated by JIS K6720-2 by dissolving 200 mg of the resin in 50 ml of nitrobenzene and measuring the specific viscosity of this polymer solution in a constant temperature tank of 30° C. by using a Ubbelohde viscometer.
- the vinyl chloride fibers are particularly preferably fibers prepared by melt spinning an ethylene/vinyl chloride copolymer resin having an ethylene content of from 0.5 to 3 mass %.
- an ethylene/vinyl chloride copolymer resin is a copolymer resin obtainable by a polymerization reaction of vinyl chloride monomer with ethylene monomer, wherein the ethylene content is from 0.5 to 3 mass %, preferably from 0.8 to 2.5 mass %. If the ethylene content is less than 0.5 mass %, the effect to suppress the nozzle pressure and gumming tends to be hardly obtainable. On the other hand, if it exceeds 3 mass %, the fibers tend to be susceptible to thermal shrinkage.
- the ethylene content is measured in accordance with the GTP-002 method.
- a resin composition having the above-mentioned ethylene/vinyl chloride copolymer resin mixed with a vinyl chloride resin other than the ethylene/vinyl chloride copolymer resin is subjected to melt spinning, whereby it is possible to impart the curl-retaining property to the fibers.
- the proportion of the vinyl chloride resin mixed is preferably at most 40 mass %, more preferably at most 35 mass %. If the proportion of the vinyl chloride resin exceeds 40 mass %, the effect to suppress gumming at the time of melt spinning may not sometimes be obtainable.
- known compounding agents may be incorporated, such as a thermal stabilizer, a processing aid, a reinforcing agent, an ultraviolet absorber, an antioxidant, a plasticizer, an antistatic agent, a filler, a flame retardant and a pigment.
- a special compounding agent such as a blowing agent, a crosslinking agent, an adhesion-imparting agent, a hydrophilicity-imparting agent, an electrical conductivity-imparting agent or a perfume may also be added, as the case requires, within a range not to impair the purpose of the present invention.
- thermal stabilizer one or more may be selected for use among thermal stabilizers including, for example, a Ca—Zn type thermal stabilizer, a hydrotalcite type thermal stabilizer, a tin type thermal stabilizer and a zeolite type thermal stabilizer. It is particularly preferred to use a combination of a Ca—Zn type thermal stabilizer and a hydrotalcite type thermal stabilizer, which is excellent in balance of the molding processability and fiber properties, and it is preferred to use such a combination in an amount of from 0.5 to 5.0 parts by mass per 100 parts by mass of the vinyl chloride resin.
- plasticizer one or more may be selected fro use among plasticizers including, for example, an epoxy plasticizer, a phthalic acid plasticizer, an adipic acid plasticizer, a polyester plasticizer, a phosphate plasticizer, a stearic acid plasticizer, a trimellitic acid plasticizer and a pyromellitic plasticizer.
- plasticizers including, for example, an epoxy plasticizer, a phthalic acid plasticizer, an adipic acid plasticizer, a polyester plasticizer, a phosphate plasticizer, a stearic acid plasticizer, a trimellitic acid plasticizer and a pyromellitic plasticizer.
- an epoxy plasticizer which is less influential over the elongation, and it is preferred to use such a plasticizer in an amount of from 0.2 to 3.0 parts by mass per 100 parts by mass of the vinyl chloride resin.
- a lubricant may be used depending upon the purpose.
- a conventional one may be used, but it may particularly be one or a mixture of at least two selected from a metal soap type lubricant, a higher fatty acid type lubricant and a polyethylene type lubricant.
- the metal soap type lubricant may, for example, be a metal soap such as a stearate, laurate or oleate of e.g. Na, Ca, Zn, Ba or Mg.
- the higher fatty acid type lubricant may, for example, be a fatty acid ester of an alcohol or a polyhydric alcohol, such as hydrogenated oil, butyl stearate, stearic acid monoglyceride, pentaerythritol tetrastearate or stearyl stearate.
- the polyethylene type lubricant is not particular limited, and a known lubricant may be used. Particularly preferred is a high density polyethylene lubricant having an average molecular weight of from 2,000 to 6,000 and density of from 0.95 to 0.98.
- Fibers (A) having sectional shapes Y-, U- and C-shapes have a high symmetry in their sectional shapes, and in the same fineness, they have a porosity higher than fibers (B) having a spectacled sectional shape, whereby their rigidity is high, and they are suitable to obtain more uniform curling.
- a flexural rigidity is measured by e.g. the KES method.
- the KES method is an abbreviation of Kawabata Evaluation System and is designed to measure the repulsion at each curvature when the fibers were flexed by means of a flexural property measuring apparatus (manufactured by KATO TECH CO., LTD.) by the KES method as disclosed by Sueo Kawabata in the journal of Textile Machinery Society (Textile Engineering), vol. 26, No. 10, p. 721-p. 728 (1973).
- a method for controlling the value of the flexural rigidity by the KES method it is possible to adopt, for example, a method of controlling the spinneret temperature of nozzles at the time of melt-spinning fibers (A) and (B). Although the reason is not clearly understood, it is possible to lower the flexural rigidity by lowering the spinneret temperature of the nozzles.
- control can be attained by changing the fineness of the fiber. Namely, by reducing the fineness, the flexural rigidity can be made low. On the other hand, by enlarging the fineness, the flexural rigidity can be made high.
- the flexural rigidity of fibers (A) by the KES method is (1.2 to 3.5) ⁇ 10 ⁇ 2 N ⁇ cm 2 , preferably (1.8 to 2.5) ⁇ 10 ⁇ 2 N ⁇ cm 2 .
- the flexural rigidity of fibers (B) by the KES method is (0.5 to 1.0) ⁇ 10 ⁇ 2 N ⁇ cm 2 , preferably (0.7 to 0.8) ⁇ 10 ⁇ 2 N ⁇ cm 2 .
- the flexural rigidity of fibers (A) by the KES method is smaller than 1.2 ⁇ 10 ⁇ 2 N cm 2 , the curling uniformity tends to be inferior, and if it exceeds 3.5 ⁇ 10 ⁇ 2 N ⁇ cm 2 , the touch tends to be hard, such being not suitable for a fiber bundle for artificial hair. Further, if the flexural rigidity of fibers (B) by the KES method is less than 0.5 ⁇ 10 ⁇ 2 N ⁇ cm 2 , the curling uniformity tends to be inferior, and if it exceeds 1.0 ⁇ 10 ⁇ 2 N ⁇ cm 2 , the touch tends to be hard, such being not suitable for a fiber bundle for artificial hair.
- the fibers (A) and the fibers (B) are preferably vinyl chloride fibers made of a vinyl chloride resin.
- the vinyl chloride fibers resemble natural hair in the gloss, strength, elongation and specific gravity, and their touch is soft, whereby they are preferred as a fiber bundle for artificial hair.
- vinyl chloride resin constituting the vinyl chloride fibers one having the above-described construction and physical properties can be suitably employed.
- the fibers (A) are more preferably from 80 to 50 mass %.
- Mixing of the fibers (A) and (B) may be carried out during the spinning or at the time of secondary processing. However, in order to obtain a uniform blend to attain the gloss and tough like natural hair, it is preferred to mix them during spinning from mixed nozzles (circular spinneret) wherein a number of nozzles for fibers (A) and (B) are disposed.
- the sectional shape of the fibers (A) is at least one selected from the group consisting of Y-, U- and C-shapes. These sectional shapes are highly symmetric and have a porosity relatively larger than e.g. a circular shape at the same fineness, and thus they are suitable to obtain high rigidity and more uniform curling.
- Y-shape is a shape having three projections radially extending from the center portion in the cross section of a fiber and represents, for example, the shape shown in FIG. 1 .
- the lengths of the projections may be the same or different and may have a dent of recess.
- the angle ⁇ between the projections is preferably from 90 to 140°, more preferably from 110 to 130°.
- the cross-sectional shape is such that the total angle of three ⁇ becomes 360°, and the radius of the circumscribed circle becomes from 2 to 4 times the radius of the inscribed circle.
- U-shape is a semi-hollow shape with a circular arc having an opening, in the cross section of a fiber and represents, for example, the shape shown in FIG. 2 .
- the thickness of the circular arc portion may be the same or varied and may be asymmetric, and the ends of the opening may be rounded or angular. Further, the width of the opening is preferably the same as the diameter of the center portion of the hollow.
- the C-shape represents a fiber having an “opened hollow” sectional shape perpendicular to the longitudinal axis of the fiber and having a circular arc in the cross section of the fiber.
- the “opened hollow” represents a generally C-shaped section having the center portion of the hollow and the solid region extending around the center portion to define the wall portion surrounding the center portion, and the opening on one side of the wall portion connects the center portion to the outside of the fiber.
- the opening is narrower than the diameter of the center portion of the hollow, whereby a throat or narrowed portion is formed between the center portion of the hollow and the outside of the fiber. It represents, for example, the shape shown in FIG. 3 .
- the thickness of the circular arc portion may be the same or varied and may be asymmetric, and the ends of the opening may be rounded or angular.
- the sectional shape of the fibers (B) is preferably a spectacled shape, and the spectacled shape is suitable for a fiber bundle for artificial hair, since not only a soft touch like natural hair is thereby obtainable, but also a plastic-like gloss is thereby little.
- the spectacled shape is a shape having two circles or ellipses continuously positioned and connected by a bridge, and it represents, for example, the spectacled shape of FIG. 4 or an ellipsoidal spectacled shape of FIG. 5 .
- the circles or the ellipses may have a dent or recess, and the centers of the circles or the ellipses and the center of the connecting portion may be in parallel or not in parallel.
- the connecting bridge is preferably the same as or up to 1.8 times the radius of the circles or the half of the average of the long axis and short axis of the ellipses, and the contact points of the bridge with the circles are preferably always curved in an arc.
- the continuous circles are preferably adjacent to each other to such an extent that the arcs of the circles are in contact with each other, and ones which are extremely apart from each other or ones of which the arcs overlap each other are not desirable.
- a vinyl chloride resin composition as the starting material may be used in the form of a powder compound prepared by mixing by means of a conventional mixing machine such as a Henschel mixer, a super mixer or a is ribbon blender, or in the form of a pellet compound prepared by melt-mixing such a powder compound.
- the powder compound may be prepared under conventional conditions, and the preparation may be hot blending or cold blending. Particularly preferably, hot blending is used wherein the cutting temperature at the time of blending is raised to a level of from 105 to 155° C. in order to reduce the volatile component in the resin composition.
- the pellet compound can be prepared in the same manner as the preparation of a usual vinyl chloride type pellet compound.
- a kneader such as a single screw extruder, a counter-rotating twin screw extruder, a conical twin screw extruder, a co-rotating twin screw extruder, a co-kneader, a planetary gear extruder or a roll kneader
- the pellet compound may be prepared.
- the conditions for preparing the pellet compound are not particularly limited, but it is preferred to set them so that the resin temperature will be at most 185° C.
- the fibers (A) and (B) are preferably processed by melt spinning, and nozzles to be used may suitably be selected taking into consideration the expansion due to the Burns effect at the time when the molten resin is extruded from the nozzles and/or the reduction of the sectional shape due to drawing exerted to the fibers at the time of spinning.
- the polyvinyl chloride resin has a good shaping property, and by using nozzles having a nozzle hole shape close to the sectional shape of the desired fibers of the present invention, the fibers (A) and (B) will be obtained.
- melt spinning can be carried out by using conventional nozzles.
- strands are melt-extruded from a plurality of nozzle holes of multi-type nozzles having a sectional area of at most 0.5 mm 2 per nozzle hole to produce non-stretched fibers having at most 300 decitex.
- non-stretched fibers may be obtained also by melt-spinning a pellet compound or the like, of the resin composition at a temperature of from 160 to 190° C., for example, by using a single screw extruder.
- the conditions for stretch treatment are preferably such that the non-stretched fibers are stretched from 2 to 4 times in an atmosphere of air held at a temperature of from 90 to 120° C., and then the stretched fibers are annealed in an atmosphere of air held at a temperature of from 110 to 140° C. until they become to have a length of from 60 to 100% of the length before the annealing.
- the fibers having stretch treatment and thermal treatment applied to the non-stretched fibers are preferably such that the fineness of each fiber is preferably from 20 to 100 decitex, more preferably from 50 to 80 decitex. When the fineness is from 20 to 100 decitex, the fiber is comparable to natural hair, and when it is from 50 to 80 decitex, it will be one having the touch and texture further improved.
- the “nozzle pressure” is an index as to whether or not, when continuous spinning is carried out, the spinning can be carried out in a stabilized state for a long period of time.
- the “nozzle pressure” is a resin pressure measured at nozzles when continuous spinning is carried out for 24 hours, and it was evaluated by the following standards.
- the nozzle pressure is at most 40 MPa, whereby the production can be constantly carried out, and there is no problem in the long running property.
- the “gumming time” is an index for the production time until the production becomes difficult as fiber breakage starts due to gumming and the gumming is wiped off.
- the “gumming time” was evaluated by the following standards.
- Excellent It is at least 36 hours, whereby the production can be carried out constantly, and there is no problem in the long running property at all.
- Good It is from 24 to 36 hours, whereby the production can be carried out constantly, and there is no problem in the long running property.
- No good It is less than 24 hours, and there is a problem in the long running property to carry out the production constantly.
- the “coloration” is the color of fibers immediately after the continuous spinning, as visually observed, and it was evaluated by the following standards.
- the “curl-retention” was evaluated under the following standards by putting fibers in a hot air dryer at 90° C. for 60 minutes in a state where the fibers are wound on an aluminum pipe with their forward end fixed, thereafter taking them out, suspending them for 24 hours in a state at a temperature of 23° C. under a relative humidity of 50° C., and measuring the distance of the movement of the suspended forward end before and after the suspension. The shorter the distance of this movement, the better the curl-retention.
- Excellent The distance of movement of the forward end is at most 1.5 cm.
- Good The distance of movement of the forward end is more than 1.5 cm and less than 3.0 cm.
- No good The distance of movement of the forward end is at least 3.0 cm.
- the “thermal shrinkage” means the thermal shrinkage which takes place when a test specimen is thermally treated.
- the test for the thermal shrinkage is carried out by subjecting a test sample adjusted to a length of 100 mm to thermal treatment for 15 minutes in a gear oven of 90° C. and measuring the length of the test sample before and after the thermal treatment.
- the thermal shrinkage is obtained from the obtained length by the following formula.
- the number of test samples was ten, and the average value was evaluated by the following standards.
- the average value of thermal shrinkage is at most 5%, whereby there is no problem at all from the viewpoint of the product quality.
- Good The average value of thermal shrinkage is more than 5% and less than 10%, and there is no problem from the viewpoint of the product quality.
- No good The average value of the thermal shrinkage is at least 10%, whereby there is a problem from the viewpoint of the product quality.
- Fibers for artificial hair having a fineness of 67 decitex were obtained by sequentially carrying out (a) a step of mixing by a Henschel mixer a resin composition prepared by blending 100 parts by mass of an ethylene/vinyl chloride copolymer resin (manufactured by Taiyo Vinyl Corp., TE-1300; ethylene content: 1.5 mass %, viscosity average polymerization degree: 1,300), 8 parts by mass of a hydrotalcite type composite thermal stabilizer (manufactured by Nissan Chemical Industries, Ltd., CP-410A) (thermal stabilizer component being 4 parts by mass %), and 1 part by mass of epoxidized soybean oil (ADECA CORPORATION, 0-130P), (b) a step of melt spinning the mixed resin composition at a spinneret temperature of 180° C.
- a Henschel mixer a resin composition prepared by blending 100 parts by mass of an ethylene/vinyl chloride copolymer resin (manufactured by Taiyo Vinyl
- Fibers for artificial hair having ethylene contents as identified in Table 1-1 were obtained in the same manner as in Example 1-1.
- Fibers for artificial hair having the ethylene content adjusted to be 1.5 times of Example 1-1 and having the viscosity average polymerization degree of the ethylene/vinyl chloride copolymer as shown in Table 1-2, were obtained in the same manner as in Example 1-1.
- Fibers for artificial hair having a vinyl chloride resin content as identified in Table 1-3 were obtained in the same manner as in Example 1-1.
- the fibers for artificial hair of the present invention can be constantly produced under a low nozzle pressure with little gumming, and the curl retention is excellent.
- the “flexural rigidity” was measured by using KES-FB2 pure bending tester (manufactured by KATO TECH CO., LTD.). Namely, one fiber having a length of 9 cm, of the fibers (A) or (B), was passed through a jig having a diameter of 0.2 mm and subjected to a pure bending test at a deformation rate of 0.2 (cm ⁇ 1 ) within a curvature range of from ⁇ 2.5 to +2.5 (cm ⁇ 1 ), and an average value of repulsion with one fiber within a curvature range of from 0.5 to 1.5 (cm ⁇ 1 ) was measured.
- the difference in curl pitch is smaller than 10 mm, such being suitable for an article required to have a tight curl.
- Good The difference in curl pitch is from 10 to 20 mm, and uniform curling is obtainable.
- No good The difference in curl pitch is larger than 20 mm, and curling is non-uniform.
- the “tough” represents the touch when 24,000 fibers comprising fibers (A) and (B) are bundled, and the fibers are frictioned one another, and it was evaluated by the following standards.
- the touch is soft resembling natural hair.
- Good The touch is slightly soft resembling natural hair.
- No good The touch is stiff and hard.
- Fibers having 160 decitex were obtained by melt spinning a resin composition prepared by blending 100 parts by mass of a vinyl chloride resin (manufactured by Taiyo Vinyl Corp., TH-1000), 3 parts by mass of a hydrotalcite type composite thermal stabilizer (manufactured by Nissan Chemical Industries, Ltd., CP-410A) (thermal stabilizer component being 1.5 parts by mass), 0.5 part by mass of epoxidized soybean oil (manufactured by ADECA CORPORATION, O-130P) and 0.8 part by mass of an ester type lubricant (manufactured by Riken Vitamin Co., Ltd., EW-100) by means of mixed nozzles (circular spinning spinneret having a nozzle section shown in FIG.
- a resin composition prepared by blending 100 parts by mass of a vinyl chloride resin (manufactured by Taiyo Vinyl Corp., TH-1000), 3 parts by mass of a hydrotalcite type composite thermal stabilizer (manufactured by Nissan Chemical
- the fibers obtained by the melt spinning were subjected to stretching in an atmosphere of air at 105° C. to 300%. Then, they were thermally treated in an atmosphere of air at 110° C. until the entire length of the fibers shrunk to a length of 75% of the length before the treatment.
- Y-sectional shape fibers having a flexural rigidity of 2.0 ⁇ 10 ⁇ 2 N ⁇ cm 2 and a fineness of 71 decitex as fibers (A) and spectacled sectional shape fibers having a flexural rigidity of 0.8 ⁇ 10 ⁇ 2 N ⁇ cm 2 and a fineness of 71 decitex as fibers (B) were obtained.
- the product was a fiber bundle for artificial hair comprising 70 mass % of the fibers (A) and 30 mass % of the fibers (B).
- Fiber bundles for artificial hair having the sectional shapes and mass % of the fibers (A) and the fibers (B) as identified in Tables 2-1 and 3-1 were obtained in the same manner as in Example 2-1.
- Fiber bundles for artificial hair were obtained in the same manner as in Example 2-1 except that the sectional shape of the fibers (A) was Y-shape of FIG. 1 and no fibers (B) were contained.
- a fiber bundle for artificial hair was obtained in the same manner as in Example 2-1 except that the sectional shape of the fibers (B) was a spectacled shape of FIG. 4 and no fibers (A) were contained.
- Fiber bundles for artificial hair were obtained in the same manner as in Example 2-1 except that in Comparative Example 2-3, the spinneret temperature was changed to 160° C., and in Comparative Example 2-4, the spinneret temperature was changed to 180° C.
- Fiber bundles for artificial hair were obtained in the same manner as in Example 2-1 except that in Comparative Example 2-5, the fineness of the fibers (A) and the fibers (B) was changed to 100 decitex, and in Comparative Example 2-6, the fineness of the fibers (A) and the fibers (B) was changed to 220 decitex.
- the fibers for artificial hair and the fiber bundle for artificial hair of the present invention can be suitably employed for hair decoration articles such as wigs, hairpieces, braids, extension hair, accessory hair and doll hair.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Mechanical Engineering (AREA)
- Artificial Filaments (AREA)
Abstract
Description
- The present invention relates to a fiber bundle of artificial hair to be used for hair decoration articles such as wigs, hairpieces, braided hair, extension hair, accessory hair or doll hair, and a head decoration article employing it. Units such as “parts” and “%” showing a blend composition of a resin composition will be represented by mass unless otherwise specified.
- Vinyl chloride resin fibers obtained by spinning a vinyl chloride resin are excellent in transparency and flexibility and thus are widely used as fibers for artificial hair to be used for head decoration articles such as wigs. For industrial production of vinyl chloride resin fibers, a wet spinning method of spinning a vinyl chloride resin by using an organic solvent, a dry spinning method or a melt spinning method of melt-spinning it without using an organic solvent, has been known.
- The melt spinning method is a method of extruding the resin at a high temperature under a high pressure by using an extruder. A vinyl chloride resin has a high melt viscosity and an extremely low spinning property, and thus, there has been a problem such that it is difficult to melt-spin the vinyl chloride resin to obtain vinyl chloride resin fibers having a prescribed quality.
- As an industrial process, strands are extruded from nozzle holes having a small sectional area per hole, introduced into a heating cylinder and heat-melted and drawn therein to obtain unstretched fibers. However, they are discharged from nozzle holes having a small sectional area per hole, whereby there has been a problem that the pressure exerted to the nozzles tends to be high and is likely to exceed the pressure designed for the extruder, or there has been a problem such that gumming (scales around the nozzles) is likely to result. In order to solve such problems, a means to incorporate a plasticizer and a vinyl chloride homopolymer having a low degree of polymerization has been proposed (e.g. Patent Document 1).
- Further, fiber bundles for artificial hair processed by using the above-mentioned fibers for artificial hair, are used as head decoration articles. Such fiber bundles for artificial hair are selected from those wherein the sectional shape of fibers is circular, oval, horseshoe, a cocoon-shape, a ribbon-shape or a star-shape, depending upon the properties such as the touch, the appearance, the gloss and the esthetic functionality attributable to human hair. Further, the head decoration articles are generally classified into three styles of short, medium and long, and the required functions are different depending upon the styles. It has been common to modify the sectional shape of fibers to meet such requirements. However, with a single sectional shape, it has been impossible to meet the requirements of a wide range of hairstyles.
- In order to improve uniformity of curling to meet such requirements, a method to have a three-pronged sectional shape (e.g. Patent Document 2), a method to have a hollow section (e.g. Patent Document 3) or a method of mixing fibers having three types of sectional shapes (e.g. Patent Document 4) has been proposed.
- Patent Document 1: JP-A-11-61555
- Patent Document 2: JP-U-58-37961
- Patent Document 3: JP-U-63-48652
- Patent Document 4: JP-B-58-13641
- It is an object of the present invention to provide a fiber bundle for artificial hair having a soft touch close to human hair while maintaining uniform curling, by using fibers for artificial hair prepared under a low nozzle pressure with little gumming and by mixing a plurality of fibers different in the sectional shape of the fibers for artificial hair, and a head decoration article comprising such a fiber bundle.
- The present inventors have conducted an extensive study to accomplish the above object and as a result, have found that by mixing fibers having rigidities within certain ranges, a fiber bundle for artificial hair employing fibers for artificial hair made of vinyl chloride fibers, exhibits merits as a head decoration article effectively. Further, it has been found that as the above vinyl chloride fibers, fibers for artificial hair prepared under a low nozzle pressure with little gumming, are obtainable by melt-spinning a specific ethylene/vinyl chloride copolymer resin.
- The present invention has been made on the basis of the above discoveries and provides the following.
- (1) A fiber bundle for artificial hair comprising fibers (A) having a flexural rigidity of (1.2 to 3.5)×10−2 N cm2 as determined by the KES method and fibers (B) having a flexural rigidity of (0.5 to 1.0)×10−2 N cm2 as determined by the KES method, wherein both of the fibers (A) and the fibers (B) are made of vinyl chloride fibers.
(2) The fiber bundle for artificial hair according to the above (1), wherein the content of the fibers (A) is from 30 to 90 mass %.
(3) The fiber bundle for artificial hair according to the above (1) or (2), wherein the sectional shape of the fibers (A) is at least one selected from the group consisting of Y-, U- and C-shapes.
(4) The fiber bundle for artificial hair according to any one of the above (1) to (3), wherein the sectional shape of the fibers (B) is a spectacled sectional shape.
(5) The fiber bundle for artificial hair according to any one of the above (1) to (4), wherein the vinyl chloride fibers are made of fibers prepared by melt spinning an ethylene/vinyl chloride copolymer resin having an ethylene content of from 0.5 to 3 mass %.
(6) The fiber bundle for artificial hair according to the above (5), wherein the viscosity-average polymerization degree of the ethylene/vinyl chloride copolymer resin is from 900 to 2,500.
(7) The fiber bundle for artificial hair according to the above (5) or (6), wherein the vinyl chloride fibers are made of fibers prepared by melt spinning a mixed resin of the ethylene/vinyl chloride copolymer resin and a vinyl chloride resin other than the ethylene/vinyl chloride copolymer resin.
(8) The fiber bundle for artificial hair according to the above (7), wherein the content of the vinyl chloride resin in the mixed resin is at most 40 mass %.
(9) The fiber bundle for artificial hair according to the above (7) or (8), wherein the viscosity-average polymerization degree of the vinyl chloride resin is from 600 to 2500.
(10) A head decoration article comprising the fiber bundle of artificial hair as defined in any one of the above (1) to (9). - According to the present invention, it is possible to easily obtain fibers for artificial hair prepared under a low nozzle pressure with little gumming, and it is further possible to obtain a fiber bundle for artificial hair having a soft touch close to human hair, while maintaining uniform curling.
-
FIG. 1 is a schematic sectional view of a nozzle shape for fibers having a Y-shape cross section and the obtained fibers, representing one embodiment of the fiber bundle for artificial hair of the present invention. -
FIG. 2 is a is a schematic sectional view of a nozzle shape for fibers having a U-shape cross section and the obtained fibers, representing one embodiment of the fiber bundle for artificial hair of the present invention. -
FIG. 3 is a schematic sectional view of a nozzle shape for fibers having a C-shape cross section and the obtained fibers, representing one embodiment of the fiber bundle for artificial hair of the present invention. -
FIG. 4 is a schematic sectional view of a nozzle shape for fibers having a spectacled-shape cross section and the obtained fibers, representing one embodiment of the fiber bundle for artificial hair of the present invention. -
FIG. 5 is a schematic sectional view of a nozzle shape for fibers having an oval spectacled-shape cross section and the obtained fibers, representing one embodiment of the fiber bundle for artificial hair of the present invention. -
FIG. 6 is a schematic sectional view of a nozzle shape for fibers having a five leaf-shape cross section and the obtained fibers, representing one embodiment of the fiber bundle for artificial hair of the present invention. -
FIG. 7 is a schematic sectional view of a nozzle shape for fibers having a rod-shape cross section and the obtained fibers, representing one embodiment of the fiber bundle for artificial hair of the present invention. -
-
- 11: Radius of inscribed circle
- 12: Radius of circumscribed circle
- The fiber bundle for artificial hair of the present invention is composed of vinyl chloride fibers prepared by melt spinning a vinyl chloride resin. The vinyl chloride resin may be obtained by e.g. bulk polymerization, solution polymerization, suspension polymerization or emulsion polymerization. However, in consideration of e.g. the initial coloration of fibers, it is preferred to use ones prepared by suspension polymerization. The vinyl chloride resin may be a homopolymer resin which is a conventional homopolymer of vinyl chloride or various types of conventional copolymer resins and is not particularly limited. The copolymer resins are conventional copolymer resins including, for example, a copolymer resin of vinyl chloride with a vinyl ester, such as a vinyl chloride/vinyl acetate copolymer resin or a vinyl chloride/vinyl propionate copolymer resin, a copolymer resin of vinyl chloride with an acrylate, such as a vinyl chloride/butyl acrylate copolymer resin or a vinyl chloride/2-ethylhexyl acrylate copolymer resin, a copolymer resin of vinyl chloride with an olefin such as a vinyl chloride/ethylene copolymer resin or a vinyl chloride/propylene copolymer resin, and a vinyl chloride/acrylonitrile copolymer resin.
- It is particularly preferred to use a homopolymer resin which is a homopolymer of vinyl chloride, or a vinyl chloride/vinyl acetate copolymer resin. In the copolymer resin, the content of the comonomer is not particularly limited and may be determined depending upon the required product quality such as the molding processability, fiber properties, etc.
- The vinyl chloride resin to be used in the present invention is preferably a homopolymer resin which is a homopolymer of vinyl chloride, a vinyl chloride/ethylene copolymer resin or a vinyl chloride/vinyl acetate copolymer resin. In the copolymer resin, the content of the comonomer is not particularly limited and may be determined depending upon the required product quality such as the molding processability, fiber properties, etc.
- The viscosity average polymerization degree of the vinyl chloride resin is preferably from 600 to 2,500, more preferably from 900 to 2,500, particularly preferably from 1,000 to 2,000. If it is less than 600, the melt viscosity tends to be low, and the obtained fibers tend to be susceptible to thermal shrinkage. On the other hand, if it exceeds 2,500, the melt viscosity tends to be high, and the molding temperature of the fibers tends to be high, whereby coloration of fibers may sometimes result. Here, the viscosity average polymerization degree is one calculated by JIS K6720-2 by dissolving 200 mg of the resin in 50 ml of nitrobenzene and measuring the specific viscosity of this polymer solution in a constant temperature tank of 30° C. by using a Ubbelohde viscometer.
- The vinyl chloride fibers are particularly preferably fibers prepared by melt spinning an ethylene/vinyl chloride copolymer resin having an ethylene content of from 0.5 to 3 mass %. Such an ethylene/vinyl chloride copolymer resin is a copolymer resin obtainable by a polymerization reaction of vinyl chloride monomer with ethylene monomer, wherein the ethylene content is from 0.5 to 3 mass %, preferably from 0.8 to 2.5 mass %. If the ethylene content is less than 0.5 mass %, the effect to suppress the nozzle pressure and gumming tends to be hardly obtainable. On the other hand, if it exceeds 3 mass %, the fibers tend to be susceptible to thermal shrinkage. The ethylene content is measured in accordance with the GTP-002 method.
- Further, in the present invention, a resin composition having the above-mentioned ethylene/vinyl chloride copolymer resin mixed with a vinyl chloride resin other than the ethylene/vinyl chloride copolymer resin, is subjected to melt spinning, whereby it is possible to impart the curl-retaining property to the fibers. The proportion of the vinyl chloride resin mixed is preferably at most 40 mass %, more preferably at most 35 mass %. If the proportion of the vinyl chloride resin exceeds 40 mass %, the effect to suppress gumming at the time of melt spinning may not sometimes be obtainable.
- In the present invention, to the above resin composition, known compounding agents may be incorporated, such as a thermal stabilizer, a processing aid, a reinforcing agent, an ultraviolet absorber, an antioxidant, a plasticizer, an antistatic agent, a filler, a flame retardant and a pigment. Further, a special compounding agent such as a blowing agent, a crosslinking agent, an adhesion-imparting agent, a hydrophilicity-imparting agent, an electrical conductivity-imparting agent or a perfume may also be added, as the case requires, within a range not to impair the purpose of the present invention.
- As the above thermal stabilizer, one or more may be selected for use among thermal stabilizers including, for example, a Ca—Zn type thermal stabilizer, a hydrotalcite type thermal stabilizer, a tin type thermal stabilizer and a zeolite type thermal stabilizer. It is particularly preferred to use a combination of a Ca—Zn type thermal stabilizer and a hydrotalcite type thermal stabilizer, which is excellent in balance of the molding processability and fiber properties, and it is preferred to use such a combination in an amount of from 0.5 to 5.0 parts by mass per 100 parts by mass of the vinyl chloride resin.
- As the above plasticizer, one or more may be selected fro use among plasticizers including, for example, an epoxy plasticizer, a phthalic acid plasticizer, an adipic acid plasticizer, a polyester plasticizer, a phosphate plasticizer, a stearic acid plasticizer, a trimellitic acid plasticizer and a pyromellitic plasticizer. Particularly preferred is an epoxy plasticizer which is less influential over the elongation, and it is preferred to use such a plasticizer in an amount of from 0.2 to 3.0 parts by mass per 100 parts by mass of the vinyl chloride resin.
- In the present invention, a lubricant may be used depending upon the purpose. As such a lubricant, a conventional one may be used, but it may particularly be one or a mixture of at least two selected from a metal soap type lubricant, a higher fatty acid type lubricant and a polyethylene type lubricant. The metal soap type lubricant may, for example, be a metal soap such as a stearate, laurate or oleate of e.g. Na, Ca, Zn, Ba or Mg. The higher fatty acid type lubricant may, for example, be a fatty acid ester of an alcohol or a polyhydric alcohol, such as hydrogenated oil, butyl stearate, stearic acid monoglyceride, pentaerythritol tetrastearate or stearyl stearate. The polyethylene type lubricant is not particular limited, and a known lubricant may be used. Particularly preferred is a high density polyethylene lubricant having an average molecular weight of from 2,000 to 6,000 and density of from 0.95 to 0.98.
- In the present invention, to maintain curling to be uniform, rigidity in the fiber bundle state is required. However, only with fibers having strong rigidity, curling may be made to be uniform, but the soft touch required for the fiber bundle tends to be inferior. On the other hand, only with soft fibers having weak rigidity, the touch may be excellent, but uniform curling as a head decoration article tends to be inferior. By mixing fibers having strong rigidity and fibers having weak rigidity, it is possible to obtain a fiber bundle for artificial hair having a soft touch close to human hair while maintaining uniform curling, taking the advantages of both fibers. Fibers (A) having sectional shapes Y-, U- and C-shapes have a high symmetry in their sectional shapes, and in the same fineness, they have a porosity higher than fibers (B) having a spectacled sectional shape, whereby their rigidity is high, and they are suitable to obtain more uniform curling.
- Here, with respect to the rigidity, a flexural rigidity is measured by e.g. the KES method. The KES method is an abbreviation of Kawabata Evaluation System and is designed to measure the repulsion at each curvature when the fibers were flexed by means of a flexural property measuring apparatus (manufactured by KATO TECH CO., LTD.) by the KES method as disclosed by Sueo Kawabata in the journal of Textile Machinery Society (Textile Engineering), vol. 26, No. 10, p. 721-p. 728 (1973). And, an average value of repulsion per fiber between a curvature of 0.5 (cm−1) to a curvature of 1.5 (cm−1). By measuring the repulsion per fiber, the rigidity of the fiber bundle is predictable.
- As a method for controlling the value of the flexural rigidity by the KES method, it is possible to adopt, for example, a method of controlling the spinneret temperature of nozzles at the time of melt-spinning fibers (A) and (B). Although the reason is not clearly understood, it is possible to lower the flexural rigidity by lowering the spinneret temperature of the nozzles.
- Further, such control can be attained by changing the fineness of the fiber. Namely, by reducing the fineness, the flexural rigidity can be made low. On the other hand, by enlarging the fineness, the flexural rigidity can be made high.
- In the present invention, the flexural rigidity of fibers (A) by the KES method is (1.2 to 3.5)×10−2 N·cm2, preferably (1.8 to 2.5)×10−2 N·cm2. Further, the flexural rigidity of fibers (B) by the KES method is (0.5 to 1.0)×10−2 N·cm2, preferably (0.7 to 0.8)×10−2 N·cm2. If the flexural rigidity of fibers (A) by the KES method is smaller than 1.2×10−2 N cm2, the curling uniformity tends to be inferior, and if it exceeds 3.5×10−2 N·cm2, the touch tends to be hard, such being not suitable for a fiber bundle for artificial hair. Further, if the flexural rigidity of fibers (B) by the KES method is less than 0.5×10−2 N·cm2, the curling uniformity tends to be inferior, and if it exceeds 1.0×10−2 N·cm2, the touch tends to be hard, such being not suitable for a fiber bundle for artificial hair.
- The fibers (A) and the fibers (B) are preferably vinyl chloride fibers made of a vinyl chloride resin. The vinyl chloride fibers resemble natural hair in the gloss, strength, elongation and specific gravity, and their touch is soft, whereby they are preferred as a fiber bundle for artificial hair.
- As the vinyl chloride resin constituting the vinyl chloride fibers, one having the above-described construction and physical properties can be suitably employed.
- In the present invention, by adjusting the mixing ratio of fibers (A) and fibers (B), it is possible to obtain more preferred uniform curling and soft touch. If the fibers (A) exceed 90 mass %, the touch tends to be hard, and if they are less than 30 mass %, the uniformity of curling tends to be poor. In a case where a more tight uniformity of curling is required, the fibers (A) are more preferably from 80 to 50 mass %.
- Mixing of the fibers (A) and (B) may be carried out during the spinning or at the time of secondary processing. However, in order to obtain a uniform blend to attain the gloss and tough like natural hair, it is preferred to mix them during spinning from mixed nozzles (circular spinneret) wherein a number of nozzles for fibers (A) and (B) are disposed.
- The sectional shape of the fibers (A) is at least one selected from the group consisting of Y-, U- and C-shapes. These sectional shapes are highly symmetric and have a porosity relatively larger than e.g. a circular shape at the same fineness, and thus they are suitable to obtain high rigidity and more uniform curling.
- Y-shape is a shape having three projections radially extending from the center portion in the cross section of a fiber and represents, for example, the shape shown in
FIG. 1 . The lengths of the projections may be the same or different and may have a dent of recess. The angle θ between the projections is preferably from 90 to 140°, more preferably from 110 to 130°. Further preferably, the cross-sectional shape is such that the total angle of three θ becomes 360°, and the radius of the circumscribed circle becomes from 2 to 4 times the radius of the inscribed circle. - U-shape is a semi-hollow shape with a circular arc having an opening, in the cross section of a fiber and represents, for example, the shape shown in
FIG. 2 . The thickness of the circular arc portion may be the same or varied and may be asymmetric, and the ends of the opening may be rounded or angular. Further, the width of the opening is preferably the same as the diameter of the center portion of the hollow. - C-shape represents a fiber having an “opened hollow” sectional shape perpendicular to the longitudinal axis of the fiber and having a circular arc in the cross section of the fiber. The “opened hollow” represents a generally C-shaped section having the center portion of the hollow and the solid region extending around the center portion to define the wall portion surrounding the center portion, and the opening on one side of the wall portion connects the center portion to the outside of the fiber. The opening is narrower than the diameter of the center portion of the hollow, whereby a throat or narrowed portion is formed between the center portion of the hollow and the outside of the fiber. It represents, for example, the shape shown in
FIG. 3 . The thickness of the circular arc portion may be the same or varied and may be asymmetric, and the ends of the opening may be rounded or angular. - The sectional shape of the fibers (B) is preferably a spectacled shape, and the spectacled shape is suitable for a fiber bundle for artificial hair, since not only a soft touch like natural hair is thereby obtainable, but also a plastic-like gloss is thereby little. Here, the spectacled shape is a shape having two circles or ellipses continuously positioned and connected by a bridge, and it represents, for example, the spectacled shape of
FIG. 4 or an ellipsoidal spectacled shape ofFIG. 5 . The circles or the ellipses may have a dent or recess, and the centers of the circles or the ellipses and the center of the connecting portion may be in parallel or not in parallel. However, the connecting bridge is preferably the same as or up to 1.8 times the radius of the circles or the half of the average of the long axis and short axis of the ellipses, and the contact points of the bridge with the circles are preferably always curved in an arc. Further, the continuous circles are preferably adjacent to each other to such an extent that the arcs of the circles are in contact with each other, and ones which are extremely apart from each other or ones of which the arcs overlap each other are not desirable. - A vinyl chloride resin composition as the starting material may be used in the form of a powder compound prepared by mixing by means of a conventional mixing machine such as a Henschel mixer, a super mixer or a is ribbon blender, or in the form of a pellet compound prepared by melt-mixing such a powder compound.
- The powder compound may be prepared under conventional conditions, and the preparation may be hot blending or cold blending. Particularly preferably, hot blending is used wherein the cutting temperature at the time of blending is raised to a level of from 105 to 155° C. in order to reduce the volatile component in the resin composition.
- The pellet compound can be prepared in the same manner as the preparation of a usual vinyl chloride type pellet compound. For example, by using a kneader such as a single screw extruder, a counter-rotating twin screw extruder, a conical twin screw extruder, a co-rotating twin screw extruder, a co-kneader, a planetary gear extruder or a roll kneader, the pellet compound may be prepared. The conditions for preparing the pellet compound are not particularly limited, but it is preferred to set them so that the resin temperature will be at most 185° C.
- The fibers (A) and (B) are preferably processed by melt spinning, and nozzles to be used may suitably be selected taking into consideration the expansion due to the Burns effect at the time when the molten resin is extruded from the nozzles and/or the reduction of the sectional shape due to drawing exerted to the fibers at the time of spinning. Especially in the melt spinning, the polyvinyl chloride resin has a good shaping property, and by using nozzles having a nozzle hole shape close to the sectional shape of the desired fibers of the present invention, the fibers (A) and (B) will be obtained.
- In the present invention, melt spinning can be carried out by using conventional nozzles. However, taking into consideration the quality aspect such as the curling property for artificial hair, it is preferred to carry out melt extrusion from nozzles having a sectional area of at most 0.5 mm2 per nozzle hole. If the sectional area per nozzle hole exceeds 0.5 mm2, it will be required to exert an excessive tension to form a fine non-stretched fiber or stretched fiber, whereby the residual strain will increase, and the product quality such as the curl-retention tends to deteriorate. Therefore, particularly preferably, strands are melt-extruded from a plurality of nozzle holes of multi-type nozzles having a sectional area of at most 0.5 mm2 per nozzle hole to produce non-stretched fibers having at most 300 decitex.
- Further, non-stretched fibers may be obtained also by melt-spinning a pellet compound or the like, of the resin composition at a temperature of from 160 to 190° C., for example, by using a single screw extruder.
- The conditions for stretch treatment are preferably such that the non-stretched fibers are stretched from 2 to 4 times in an atmosphere of air held at a temperature of from 90 to 120° C., and then the stretched fibers are annealed in an atmosphere of air held at a temperature of from 110 to 140° C. until they become to have a length of from 60 to 100% of the length before the annealing. The fibers having stretch treatment and thermal treatment applied to the non-stretched fibers are preferably such that the fineness of each fiber is preferably from 20 to 100 decitex, more preferably from 50 to 80 decitex. When the fineness is from 20 to 100 decitex, the fiber is comparable to natural hair, and when it is from 50 to 80 decitex, it will be one having the touch and texture further improved.
- Now, the present invention will be described in further detail with reference to Examples, but it should be understood that the present invention is by no means restricted by such Examples.
-
TABLE 1-1 Comparative Examples Examples 1-1 1-2 1-3 1-1 1-2 Ethylene content 1.5 mass % 0.5 mass % 3.0 mass % 0.3 mass % 4.0 mass % Nozzle pressure Excellent Excellent Excellent No good Excellent Gumming time Excellent Excellent Excellent No good Excellent Thermal Excellent Excellent Good Excellent No good shrinkage -
TABLE 1-2 Examples 1-1 1-4 1-5 Polymerization degree of 1300 700 2600 ethylene/vinyl chloride copolymer resin Thermal shrinkage Excellent Good Excellent Coloration Excellent Excellent Good -
TABLE 1-3 Examples 1-6 1-7 Vinyl chloride resin 30 mass % 50 mass % content Gumming time Excellent Good Curl-retention Excellent Excellent -
TABLE 1-4 Examples 1-6 1-8 1-9 Polymerization degree of 1000 500 2700 vinyl chloride resin Coloration Excellent Excellent Good Thermal shrinkage Excellent Good Excellent - In Table 1-1, the “nozzle pressure” is an index as to whether or not, when continuous spinning is carried out, the spinning can be carried out in a stabilized state for a long period of time. The “nozzle pressure” is a resin pressure measured at nozzles when continuous spinning is carried out for 24 hours, and it was evaluated by the following standards.
- Excellent: The nozzle pressure is at most 40 MPa, whereby the production can be constantly carried out, and there is no problem in the long running property.
Good: The nozzle pressure is from 40 MPa to 45 MPa, whereby the production can be constantly carried out, and there is no problem in the long running property.
No good: The nozzle pressure exceeds 45 MPa, whereby it is necessary to reduce the extruding amount in order to carry out the production constantly. - In Tables 1-1 and 1-3, the “gumming time” is an index for the production time until the production becomes difficult as fiber breakage starts due to gumming and the gumming is wiped off. The “gumming time” was evaluated by the following standards.
- Excellent: It is at least 36 hours, whereby the production can be carried out constantly, and there is no problem in the long running property at all.
Good: It is from 24 to 36 hours, whereby the production can be carried out constantly, and there is no problem in the long running property.
No good: It is less than 24 hours, and there is a problem in the long running property to carry out the production constantly. - In Tables 1-2 and 1-4, the “coloration” is the color of fibers immediately after the continuous spinning, as visually observed, and it was evaluated by the following standards.
- Excellent: No yellowing is observed, and there is no problem at all from the viewpoint of the product quality.
Good: Yellowing is observed very slightly, but there is no problem from the viewpoint of the product quality.
No good: Yellowing is observed, and there is a problem from the viewpoint of the product quality. - In Table 1-3, the “curl-retention” was evaluated under the following standards by putting fibers in a hot air dryer at 90° C. for 60 minutes in a state where the fibers are wound on an aluminum pipe with their forward end fixed, thereafter taking them out, suspending them for 24 hours in a state at a temperature of 23° C. under a relative humidity of 50° C., and measuring the distance of the movement of the suspended forward end before and after the suspension. The shorter the distance of this movement, the better the curl-retention.
- Excellent: The distance of movement of the forward end is at most 1.5 cm.
Good: The distance of movement of the forward end is more than 1.5 cm and less than 3.0 cm.
No good: The distance of movement of the forward end is at least 3.0 cm. - In the Tables 1-1, 1-2 and 1-4, the “thermal shrinkage” means the thermal shrinkage which takes place when a test specimen is thermally treated. The test for the thermal shrinkage is carried out by subjecting a test sample adjusted to a length of 100 mm to thermal treatment for 15 minutes in a gear oven of 90° C. and measuring the length of the test sample before and after the thermal treatment. The thermal shrinkage is obtained from the obtained length by the following formula.
-
Thermal shrinkage (%)=difference in length of test sample before and after thermal treatment/length of test sample before thermal treatment×100 - The number of test samples was ten, and the average value was evaluated by the following standards.
- Excellent: The average value of thermal shrinkage is at most 5%, whereby there is no problem at all from the viewpoint of the product quality.
Good: The average value of thermal shrinkage is more than 5% and less than 10%, and there is no problem from the viewpoint of the product quality.
No good: The average value of the thermal shrinkage is at least 10%, whereby there is a problem from the viewpoint of the product quality. - Now, referring to Table 1-1, the present invention will be described in detail with reference to Examples and Comparative Examples. These Examples are exemplary and by no means limit the present invention.
- Fibers for artificial hair having a fineness of 67 decitex were obtained by sequentially carrying out (a) a step of mixing by a Henschel mixer a resin composition prepared by blending 100 parts by mass of an ethylene/vinyl chloride copolymer resin (manufactured by Taiyo Vinyl Corp., TE-1300; ethylene content: 1.5 mass %, viscosity average polymerization degree: 1,300), 8 parts by mass of a hydrotalcite type composite thermal stabilizer (manufactured by Nissan Chemical Industries, Ltd., CP-410A) (thermal stabilizer component being 4 parts by mass %), and 1 part by mass of epoxidized soybean oil (ADECA CORPORATION, 0-130P), (b) a step of melt spinning the mixed resin composition at a spinneret temperature of 180° C. at an extrusion rate of 12 kg/hr by using a spinneret having 120 nozzle holes and a nozzle sectional area of 0.06 mm2, to obtain fibers of 150 decitex, (c) a step of stretching the melt-spun fibers 300% in an atmosphere of air at 1000° C. to obtain fibers of 50 decitex, and (d) a step of applying thermal relaxing treatment in an atmosphere of air at 1200° C. until the entire length of fibers shrunk to a length of 75% of the length before the treatment.
- Fibers for artificial hair having ethylene contents as identified in Table 1-1 were obtained in the same manner as in Example 1-1.
- Fibers for artificial hair having the ethylene content adjusted to be 1.5 times of Example 1-1 and having the viscosity average polymerization degree of the ethylene/vinyl chloride copolymer as shown in Table 1-2, were obtained in the same manner as in Example 1-1.
- Fibers for artificial hair having a vinyl chloride resin content as identified in Table 1-3 were obtained in the same manner as in Example 1-1.
- Fibers for artificial hair having the vinyl chloride resin content adjusted to be the same as in Example 1-6 and having the viscosity average polymerization degree of the vinyl chloride resin as identified in Table 1-4, were obtained in the same manner as in Example 1-1.
- With the fibers for artificial hair of the present invention, the fibers can be constantly produced under a low nozzle pressure with little gumming, and the curl retention is excellent.
-
TABLE 2-1 Examples 2-1 2-2 2-3 2-4 2-5 2-6 Fibers (A) Flexural 2 2 1.8 1.8 2.2/2 2.5 rigidity (×10−2) Sectional Y-shape Y-shape Five-leaf Five-leaf U-shape/ C-shape shape shape shape Y-shape Mass % 70 95 20 20 40/30 70 Fibers (B) Flexural 0.8 0.7 0.8 0.7 0.8 0.8 rigidity (×10−2) Sectional Spectacled Rod shape Spectacled Rod shape Spectacled Spectacled shape shape shape shape shape Mass % 30 5 80 80 30 30 Uniformity of curling Excellent Excellent Good Good Excellent Excellent Touch Excellent Good Excellent Good Excellent Excellent Comparative Examples 2-1 2-2 2-3 2-4 2-5 2-6 Fibers (A) Flexural 2 1 4 1.5 3 rigidity (×10−2) Sectional Y-shape Y-shape Y-shape Y-shape Y-shape shape Mass % 100 70 70 70 70 Fibers (B) Flexural 0.8 0.65 1.0 0.3 1.5 rigidity (×10−2) Sectional Spectacled Spectacled Spectacled Spectacled Spectacled shape shape shape shape shape shape Mass % 100 30 30 30 30 Uniformity of curling Excellent No good No good Good No good Excellent Touch No good Excellent Excellent No good Good No good -
TABLE 3-2 Examples Comparative Examples 3-1 3-2 3-3 3-4 3-1 3-2 Fibers (A) Sectional U-shape C-shape Y-shape/ Y-shape U-shape C-shape shape U-shape Mass % 90 25 40/30 95 100 100 Flexural 2.2 2.5 2/2.2 2 2.2 2.5 rigidity (×10−2) Fibers (B) Sectional Spectacled Spectacled Spectacled Spectacled shape shape shape shape shape Mass % 10 75 30 5 Flexural 0.8 0.8 0.8 0.8 rigidity (×10−2) Uniformity of curling Excellent Good Excellent Excellent Excellent Excellent Touch Good Excellent Excellent Good No good No good - In Tables 2-1 and 3-1, the “flexural rigidity” was measured by using KES-FB2 pure bending tester (manufactured by KATO TECH CO., LTD.). Namely, one fiber having a length of 9 cm, of the fibers (A) or (B), was passed through a jig having a diameter of 0.2 mm and subjected to a pure bending test at a deformation rate of 0.2 (cm−1) within a curvature range of from −2.5 to +2.5 (cm−1), and an average value of repulsion with one fiber within a curvature range of from 0.5 to 1.5 (cm−1) was measured.
- In Tables 2-1 and 3-1, the “uniformity of curling” was evaluated by carrying out treatment as follows. Namely, 1 g of a fiber bundle comprising the fibers (A) and (B) and having a length of 60 cm was wound at intervals of 30 mm on an aluminum pipe having a diameter of 30 mm and heated by a dry heat of 850° C. for 1 hour. Then, it was left to stand for 2 hours under a constant temperature condition (20° C., 65 RH %) as it was wound, and then, it was removed from the pipe, and the fiber bundle was suspended. Upon expiration of 24 hours after suspending the fiber bundle having curling imparted, the first and fifth curl pitches from the top were measured and “the difference in curl pitch” was obtained. The results were evaluated by the following standards.
- Excellent: The difference in curl pitch is smaller than 10 mm, such being suitable for an article required to have a tight curl.
Good: The difference in curl pitch is from 10 to 20 mm, and uniform curling is obtainable.
No good: The difference in curl pitch is larger than 20 mm, and curling is non-uniform. - In Tables 2-1 and 3-1, the “tough” represents the touch when 24,000 fibers comprising fibers (A) and (B) are bundled, and the fibers are frictioned one another, and it was evaluated by the following standards.
- Excellent: The touch is soft resembling natural hair.
Good: The touch is slightly soft resembling natural hair.
No good: The touch is stiff and hard. - Fibers having 160 decitex were obtained by melt spinning a resin composition prepared by blending 100 parts by mass of a vinyl chloride resin (manufactured by Taiyo Vinyl Corp., TH-1000), 3 parts by mass of a hydrotalcite type composite thermal stabilizer (manufactured by Nissan Chemical Industries, Ltd., CP-410A) (thermal stabilizer component being 1.5 parts by mass), 0.5 part by mass of epoxidized soybean oil (manufactured by ADECA CORPORATION, O-130P) and 0.8 part by mass of an ester type lubricant (manufactured by Riken Vitamin Co., Ltd., EW-100) by means of mixed nozzles (circular spinning spinneret having a nozzle section shown in
FIG. 1 and a nozzle section shown inFIG. 4 , at a spinneret temperature of 170° C. at an extrusion rate of 10 kg/hr. Further, the fibers obtained by the melt spinning were subjected to stretching in an atmosphere of air at 105° C. to 300%. Then, they were thermally treated in an atmosphere of air at 110° C. until the entire length of the fibers shrunk to a length of 75% of the length before the treatment. As a result, Y-sectional shape fibers having a flexural rigidity of 2.0×10−2 N·cm2 and a fineness of 71 decitex as fibers (A) and spectacled sectional shape fibers having a flexural rigidity of 0.8×10−2 N·cm2 and a fineness of 71 decitex as fibers (B) were obtained. The product was a fiber bundle for artificial hair comprising 70 mass % of the fibers (A) and 30 mass % of the fibers (B). - Fiber bundles for artificial hair having the sectional shapes and mass % of the fibers (A) and the fibers (B) as identified in Tables 2-1 and 3-1 were obtained in the same manner as in Example 2-1.
- Fiber bundles for artificial hair were obtained in the same manner as in Example 2-1 except that the sectional shape of the fibers (A) was Y-shape of
FIG. 1 and no fibers (B) were contained. - A fiber bundle for artificial hair was obtained in the same manner as in Example 2-1 except that the sectional shape of the fibers (B) was a spectacled shape of
FIG. 4 and no fibers (A) were contained. - Fiber bundles for artificial hair were obtained in the same manner as in Example 2-1 except that in Comparative Example 2-3, the spinneret temperature was changed to 160° C., and in Comparative Example 2-4, the spinneret temperature was changed to 180° C.
- Fiber bundles for artificial hair were obtained in the same manner as in Example 2-1 except that in Comparative Example 2-5, the fineness of the fibers (A) and the fibers (B) was changed to 100 decitex, and in Comparative Example 2-6, the fineness of the fibers (A) and the fibers (B) was changed to 220 decitex.
- As is evident from Tables 2-1 and 3-1, according to the present invention, it is possible to obtain fiber bundles for artificial hair which have a soft touch close to natural hair, while maintaining uniform curling.
- The fibers for artificial hair and the fiber bundle for artificial hair of the present invention can be suitably employed for hair decoration articles such as wigs, hairpieces, braids, extension hair, accessory hair and doll hair.
- The entire disclosures of Japanese Patent Application No. 2005-176083 filed on Jun. 16, 2005, Japanese Patent Application No. 2005-203957 filed on Jul. 13, 2005 and Japanese Patent Application No. 2005-203958 filed on Jul. 13, 2005 including specifications, claims, drawings and summaries are incorporated herein by reference in their entireties.
Claims (10)
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2005-176083 | 2005-06-16 | ||
| JP2005176083 | 2005-06-16 | ||
| JP2005-203957 | 2005-07-13 | ||
| JP2005-203958 | 2005-07-13 | ||
| JP2005203957 | 2005-07-13 | ||
| JP2005203958 | 2005-07-13 | ||
| PCT/JP2006/312160 WO2006135059A1 (en) | 2005-06-16 | 2006-06-16 | Fiber bundle for artificial hair and head decoration article comprising the same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20080210250A1 true US20080210250A1 (en) | 2008-09-04 |
Family
ID=37532411
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US11/917,197 Abandoned US20080210250A1 (en) | 2005-06-16 | 2006-06-16 | Fiber Bundle for Artificial Hair and Head Decoration Article Comprising the Same |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20080210250A1 (en) |
| JP (1) | JP4889635B2 (en) |
| KR (1) | KR101154906B1 (en) |
| CN (1) | CN100528017C (en) |
| AP (1) | AP2364A (en) |
| WO (1) | WO2006135059A1 (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102286800A (en) * | 2011-05-30 | 2011-12-21 | 上海瑞贝卡纤维材料科技有限公司 | Functional modified acrylic fiber for hair and preparation method thereof |
| EP3069625A4 (en) * | 2013-11-11 | 2017-04-26 | Toray Monofilament Co., Ltd. | Filament for artificial hair and artificial hair product |
| US11432607B2 (en) * | 2017-05-30 | 2022-09-06 | Denka Company Limited | Artificial hair fiber |
| US11885043B2 (en) | 2018-08-23 | 2024-01-30 | Kaneka Corporation | Acrylic fiber for artificial hair, and head decoration product including same |
| US12031240B2 (en) | 2018-11-29 | 2024-07-09 | Denka Company Limited | Fiber for artificial hair and head accessory product |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4722881B2 (en) * | 2007-05-22 | 2011-07-13 | 電気化学工業株式会社 | Synthetic fiber bundle and method for producing synthetic fiber bundle |
| KR101959635B1 (en) * | 2017-10-18 | 2019-03-18 | 에코융합섬유연구원 | Method for evaluating braiding of braid wig yarn |
| WO2025028364A1 (en) * | 2023-07-31 | 2025-02-06 | デンカ株式会社 | Fiber for artificial hair, hair decoration product, and nozzle for melt extrusion of fiber for artificial hair |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3199516A (en) * | 1963-09-12 | 1965-08-10 | Reid Meredith Inc | Process of making long haired pile fabric and making artificial hairpieces therefrom |
| US20060154062A1 (en) * | 2003-07-25 | 2006-07-13 | Toshihiro Kowaki | Flame retardant polyester fiber for artificial hair |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS536253B1 (en) * | 1970-04-18 | 1978-03-06 | ||
| JPH06104928B2 (en) * | 1988-08-18 | 1994-12-21 | 鐘淵化学工業株式会社 | Vinyl chloride fiber for hair and method for producing the same |
| JP2002227020A (en) * | 2001-01-30 | 2002-08-14 | Kanegafuchi Chem Ind Co Ltd | Artificial hair fibers and headdress products comprising them |
| JP4420819B2 (en) * | 2002-08-01 | 2010-02-24 | 株式会社カネカ | Acrylic synthetic fibers with improved stability |
| JP2004190188A (en) * | 2002-12-12 | 2004-07-08 | Tokuyama Sekisui Ind Corp | Fiber for artificial hair |
-
2006
- 2006-06-16 JP JP2007521364A patent/JP4889635B2/en not_active Expired - Fee Related
- 2006-06-16 AP AP2007004291A patent/AP2364A/en active
- 2006-06-16 KR KR1020077022945A patent/KR101154906B1/en not_active Expired - Fee Related
- 2006-06-16 WO PCT/JP2006/312160 patent/WO2006135059A1/en not_active Ceased
- 2006-06-16 US US11/917,197 patent/US20080210250A1/en not_active Abandoned
- 2006-06-16 CN CNB200680020692XA patent/CN100528017C/en not_active Expired - Fee Related
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3199516A (en) * | 1963-09-12 | 1965-08-10 | Reid Meredith Inc | Process of making long haired pile fabric and making artificial hairpieces therefrom |
| US20060154062A1 (en) * | 2003-07-25 | 2006-07-13 | Toshihiro Kowaki | Flame retardant polyester fiber for artificial hair |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102286800A (en) * | 2011-05-30 | 2011-12-21 | 上海瑞贝卡纤维材料科技有限公司 | Functional modified acrylic fiber for hair and preparation method thereof |
| EP3069625A4 (en) * | 2013-11-11 | 2017-04-26 | Toray Monofilament Co., Ltd. | Filament for artificial hair and artificial hair product |
| US11432607B2 (en) * | 2017-05-30 | 2022-09-06 | Denka Company Limited | Artificial hair fiber |
| US11885043B2 (en) | 2018-08-23 | 2024-01-30 | Kaneka Corporation | Acrylic fiber for artificial hair, and head decoration product including same |
| US12031240B2 (en) | 2018-11-29 | 2024-07-09 | Denka Company Limited | Fiber for artificial hair and head accessory product |
Also Published As
| Publication number | Publication date |
|---|---|
| CN101193567A (en) | 2008-06-04 |
| CN100528017C (en) | 2009-08-19 |
| AP2364A (en) | 2012-02-10 |
| JP4889635B2 (en) | 2012-03-07 |
| KR101154906B1 (en) | 2012-06-13 |
| AP2007004291A0 (en) | 2007-12-31 |
| KR20080016792A (en) | 2008-02-22 |
| JPWO2006135059A1 (en) | 2009-01-08 |
| WO2006135059A1 (en) | 2006-12-21 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP5552114B2 (en) | Artificial hair fiber, its use and production method | |
| CN103124812B (en) | Preparation method of polyvinyl chloride resin | |
| JPH0838513A (en) | Novel composition for dental floss | |
| US20080139705A1 (en) | Polyvinyl Chloride-Based Fiber With Excellent Style Changeability | |
| US20080210250A1 (en) | Fiber Bundle for Artificial Hair and Head Decoration Article Comprising the Same | |
| CN101300377B (en) | Shaped cross-section fibers and fibers for artificial hair made therefrom | |
| US20100040807A1 (en) | Fiber bundle for artificial hair, and process for its production | |
| TWI705164B (en) | Thermoplastic polyurethane fiber and method for producing the same | |
| WO2000043581A1 (en) | Method for producing polyester-based combined filament yarn | |
| KR101084492B1 (en) | Polyamide Fiber for Artificial Hair and Manufacturing Method Thereof | |
| JPWO2006135060A1 (en) | Artificial hair fiber, method for producing the same, and hair ornament product | |
| JP5210856B2 (en) | Method for producing vinyl chloride resin fiber | |
| JP4890256B2 (en) | Artificial hair fiber and method for producing the same | |
| JP5085116B2 (en) | Resin composition and fiber comprising the same | |
| JP2008002041A (en) | Fiber for artificial hair and method for producing the same | |
| JP2010121219A (en) | Fiber bundle, and method for producing fiber bundle | |
| CN110637112B (en) | Fibers for artificial hair | |
| JP4722881B2 (en) | Synthetic fiber bundle and method for producing synthetic fiber bundle | |
| JP4081338B2 (en) | Polypropylene-based fluid disturbed fiber and method for producing the same | |
| JP3813893B2 (en) | Method for determining the amount of chlorinated polyvinyl chloride resin added to polyvinyl chloride fiber | |
| JP2002266160A (en) | Vinyl chloride-based resin fiber | |
| JP2008248406A (en) | Fluororesin monofilament, method for producing the same and industrial woven fabric |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AS | Assignment |
Owner name: DENKI KAGAKU KOGYO KABUSHIKI KAISHA, JAPAN Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:HORIHATA, ATSUSHI;SAKURAI, AKIRA;YOSHINO, YOSHIYUKI;AND OTHERS;REEL/FRAME:020231/0079;SIGNING DATES FROM 20071105 TO 20071108 Owner name: DENKI KAGAKU KOGYO KABUSHIKI KAISHA, JAPAN Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:HORIHATA, ATSUSHI;SAKURAI, AKIRA;YOSHINO, YOSHIYUKI;AND OTHERS;SIGNING DATES FROM 20071105 TO 20071108;REEL/FRAME:020231/0079 |
|
| STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |