JP2006307355A - Fiber for artificial hair - Google Patents
Fiber for artificial hair Download PDFInfo
- Publication number
- JP2006307355A JP2006307355A JP2005128060A JP2005128060A JP2006307355A JP 2006307355 A JP2006307355 A JP 2006307355A JP 2005128060 A JP2005128060 A JP 2005128060A JP 2005128060 A JP2005128060 A JP 2005128060A JP 2006307355 A JP2006307355 A JP 2006307355A
- Authority
- JP
- Japan
- Prior art keywords
- fiber
- flame retardant
- artificial hair
- compound
- weight
- 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.)
- Granted
Links
- 239000000835 fiber Substances 0.000 title claims abstract description 137
- 210000004209 hair Anatomy 0.000 title claims abstract description 50
- 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 claims abstract description 102
- 239000003063 flame retardant Substances 0.000 claims abstract description 96
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 64
- 229920001225 polyester resin Polymers 0.000 claims abstract description 33
- 229920000728 polyester Polymers 0.000 claims abstract description 23
- 229920001400 block copolymer Polymers 0.000 claims abstract description 14
- 229920005604 random copolymer Polymers 0.000 claims abstract description 14
- 125000003118 aryl group Chemical group 0.000 claims abstract description 13
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 11
- 239000011342 resin composition Substances 0.000 claims abstract description 8
- -1 phosphate compound Chemical class 0.000 claims description 57
- 239000004645 polyester resin Substances 0.000 claims description 30
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 26
- 239000000203 mixture Substances 0.000 claims description 23
- 150000002148 esters Chemical class 0.000 claims description 18
- 229910019142 PO4 Inorganic materials 0.000 claims description 13
- 239000010452 phosphate Substances 0.000 claims description 13
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 11
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 11
- 229910052794 bromium Inorganic materials 0.000 claims description 11
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 claims description 10
- 229910052698 phosphorus Inorganic materials 0.000 claims description 10
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 9
- 239000001301 oxygen Substances 0.000 claims description 9
- 229910052760 oxygen Inorganic materials 0.000 claims description 9
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 9
- 239000004593 Epoxy Substances 0.000 claims description 8
- 239000011574 phosphorus Substances 0.000 claims description 8
- 229920001283 Polyalkylene terephthalate Polymers 0.000 claims description 7
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Natural products OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims description 6
- NSBGJRFJIJFMGW-UHFFFAOYSA-N trisodium;stiborate Chemical compound [Na+].[Na+].[Na+].[O-][Sb]([O-])([O-])=O NSBGJRFJIJFMGW-UHFFFAOYSA-N 0.000 claims description 5
- VEORPZCZECFIRK-UHFFFAOYSA-N 3,3',5,5'-tetrabromobisphenol A Chemical compound C=1C(Br)=C(O)C(Br)=CC=1C(C)(C)C1=CC(Br)=C(O)C(Br)=C1 VEORPZCZECFIRK-UHFFFAOYSA-N 0.000 claims description 4
- 239000004793 Polystyrene Substances 0.000 claims description 4
- LJCFOYOSGPHIOO-UHFFFAOYSA-N antimony pentoxide Chemical compound O=[Sb](=O)O[Sb](=O)=O LJCFOYOSGPHIOO-UHFFFAOYSA-N 0.000 claims description 4
- ZQKXQUJXLSSJCH-UHFFFAOYSA-N melamine cyanurate Chemical compound NC1=NC(N)=NC(N)=N1.O=C1NC(=O)NC(=O)N1 ZQKXQUJXLSSJCH-UHFFFAOYSA-N 0.000 claims description 4
- 229920000515 polycarbonate Polymers 0.000 claims description 4
- 239000004417 polycarbonate Substances 0.000 claims description 4
- 229920002223 polystyrene Polymers 0.000 claims description 4
- 229920005992 thermoplastic resin Polymers 0.000 claims description 4
- 229910052787 antimony Inorganic materials 0.000 claims description 3
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 claims description 3
- 239000002216 antistatic agent Substances 0.000 claims description 3
- GCTPMLUUWLLESL-UHFFFAOYSA-N benzyl prop-2-enoate Chemical class C=CC(=O)OCC1=CC=CC=C1 GCTPMLUUWLLESL-UHFFFAOYSA-N 0.000 claims description 3
- 229920001634 Copolyester Polymers 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Natural products P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims description 2
- 125000000129 anionic group Chemical group 0.000 claims description 2
- 125000002091 cationic group Chemical group 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 229910000073 phosphorus hydride Inorganic materials 0.000 claims description 2
- BIKXLKXABVUSMH-UHFFFAOYSA-N trizinc;diborate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]B([O-])[O-].[O-]B([O-])[O-] BIKXLKXABVUSMH-UHFFFAOYSA-N 0.000 claims description 2
- BNEMLSQAJOPTGK-UHFFFAOYSA-N zinc;dioxido(oxo)tin Chemical compound [Zn+2].[O-][Sn]([O-])=O BNEMLSQAJOPTGK-UHFFFAOYSA-N 0.000 claims description 2
- BHTBHKFULNTCHQ-UHFFFAOYSA-H zinc;tin(4+);hexahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Zn+2].[Sn+4] BHTBHKFULNTCHQ-UHFFFAOYSA-H 0.000 claims description 2
- 239000002453 shampoo Substances 0.000 abstract description 17
- 239000004721 Polyphenylene oxide Substances 0.000 abstract description 5
- 229920000570 polyether Polymers 0.000 abstract description 5
- 230000003247 decreasing effect Effects 0.000 abstract 2
- 229920001296 polysiloxane Polymers 0.000 description 17
- 238000000034 method Methods 0.000 description 16
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 10
- 238000004519 manufacturing process Methods 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 6
- 125000003277 amino group Chemical group 0.000 description 5
- 239000000049 pigment Substances 0.000 description 5
- 229920002994 synthetic fiber Polymers 0.000 description 5
- 239000012209 synthetic fiber Substances 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 4
- 238000004140 cleaning Methods 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 125000003700 epoxy group Chemical group 0.000 description 4
- 229910052736 halogen Inorganic materials 0.000 description 4
- 150000002367 halogens Chemical class 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 238000002074 melt spinning Methods 0.000 description 4
- 229920000139 polyethylene terephthalate Polymers 0.000 description 4
- 239000005020 polyethylene terephthalate Substances 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 230000035807 sensation Effects 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- XQKKWWCELHKGKB-UHFFFAOYSA-L calcium acetate monohydrate Chemical compound O.[Ca+2].CC([O-])=O.CC([O-])=O XQKKWWCELHKGKB-UHFFFAOYSA-L 0.000 description 3
- 229940067460 calcium acetate monohydrate Drugs 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 230000003068 static effect Effects 0.000 description 3
- 238000005809 transesterification reaction Methods 0.000 description 3
- CMQUQOHNANGDOR-UHFFFAOYSA-N 2,3-dibromo-4-(2,4-dibromo-5-hydroxyphenyl)phenol Chemical compound BrC1=C(Br)C(O)=CC=C1C1=CC(O)=C(Br)C=C1Br CMQUQOHNANGDOR-UHFFFAOYSA-N 0.000 description 2
- LLLVZDVNHNWSDS-UHFFFAOYSA-N 4-methylidene-3,5-dioxabicyclo[5.2.2]undeca-1(9),7,10-triene-2,6-dione Chemical compound C1(C2=CC=C(C(=O)OC(=C)O1)C=C2)=O LLLVZDVNHNWSDS-UHFFFAOYSA-N 0.000 description 2
- VVJKKWFAADXIJK-UHFFFAOYSA-N Allylamine Chemical compound NCC=C VVJKKWFAADXIJK-UHFFFAOYSA-N 0.000 description 2
- 229920004943 Delrin® Polymers 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 229920002821 Modacrylic Polymers 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical group [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 238000004581 coalescence Methods 0.000 description 2
- 230000003766 combability Effects 0.000 description 2
- 239000000498 cooling water Substances 0.000 description 2
- 239000004205 dimethyl polysiloxane Substances 0.000 description 2
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 2
- 230000005611 electricity Effects 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 125000004437 phosphorous atom Chemical group 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
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 2
- 229920001707 polybutylene terephthalate Polymers 0.000 description 2
- 238000006068 polycondensation reaction Methods 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 230000037452 priming Effects 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 150000003918 triazines Chemical class 0.000 description 2
- WVLBCYQITXONBZ-UHFFFAOYSA-N trimethyl phosphate Chemical compound COP(=O)(OC)OC WVLBCYQITXONBZ-UHFFFAOYSA-N 0.000 description 2
- NEXZVOLIDKSFBH-UHFFFAOYSA-N (1,1-diphenyl-2-phosphonooxyethyl) 2-methylprop-2-enoate Chemical compound C=1C=CC=CC=1C(COP(O)(O)=O)(OC(=O)C(=C)C)C1=CC=CC=C1 NEXZVOLIDKSFBH-UHFFFAOYSA-N 0.000 description 1
- MFFNRVNPBJQZFO-UHFFFAOYSA-N (2,6-dimethylphenyl) dihydrogen phosphate Chemical compound CC1=CC=CC(C)=C1OP(O)(O)=O MFFNRVNPBJQZFO-UHFFFAOYSA-N 0.000 description 1
- AQPHBYQUCKHJLT-UHFFFAOYSA-N 1,2,3,4,5-pentabromo-6-(2,3,4,5,6-pentabromophenyl)benzene Chemical group BrC1=C(Br)C(Br)=C(Br)C(Br)=C1C1=C(Br)C(Br)=C(Br)C(Br)=C1Br AQPHBYQUCKHJLT-UHFFFAOYSA-N 0.000 description 1
- OZHJEQVYCBTHJT-UHFFFAOYSA-N 1,2,3,4,5-pentabromo-6-methylbenzene Chemical compound CC1=C(Br)C(Br)=C(Br)C(Br)=C1Br OZHJEQVYCBTHJT-UHFFFAOYSA-N 0.000 description 1
- YATIGPZCMOYEGE-UHFFFAOYSA-N 1,3,5-tribromo-2-[2-(2,4,6-tribromophenoxy)ethoxy]benzene Chemical compound BrC1=CC(Br)=CC(Br)=C1OCCOC1=C(Br)C=C(Br)C=C1Br YATIGPZCMOYEGE-UHFFFAOYSA-N 0.000 description 1
- NZUPFZNVGSWLQC-UHFFFAOYSA-N 1,3,5-tris(2,3-dibromopropyl)-1,3,5-triazinane-2,4,6-trione Chemical compound BrCC(Br)CN1C(=O)N(CC(Br)CBr)C(=O)N(CC(Br)CBr)C1=O NZUPFZNVGSWLQC-UHFFFAOYSA-N 0.000 description 1
- LXIZRZRTWSDLKK-UHFFFAOYSA-N 1,3-dibromo-5-[2-[3,5-dibromo-4-(2,3-dibromopropoxy)phenyl]propan-2-yl]-2-(2,3-dibromopropoxy)benzene Chemical compound C=1C(Br)=C(OCC(Br)CBr)C(Br)=CC=1C(C)(C)C1=CC(Br)=C(OCC(Br)CBr)C(Br)=C1 LXIZRZRTWSDLKK-UHFFFAOYSA-N 0.000 description 1
- RKDVKSZUMVYZHH-UHFFFAOYSA-N 1,4-dioxane-2,5-dione Chemical compound O=C1COC(=O)CO1 RKDVKSZUMVYZHH-UHFFFAOYSA-N 0.000 description 1
- BDFBPPCACYFGFA-UHFFFAOYSA-N 2,4,6-tris(2,4,6-tribromophenoxy)-1,3,5-triazine Chemical compound BrC1=CC(Br)=CC(Br)=C1OC1=NC(OC=2C(=CC(Br)=CC=2Br)Br)=NC(OC=2C(=CC(Br)=CC=2Br)Br)=N1 BDFBPPCACYFGFA-UHFFFAOYSA-N 0.000 description 1
- CCJKFLLIJCGHMO-UHFFFAOYSA-N 2-[diethoxyphosphorylmethyl(2-hydroxyethyl)amino]ethanol Chemical compound CCOP(=O)(OCC)CN(CCO)CCO CCJKFLLIJCGHMO-UHFFFAOYSA-N 0.000 description 1
- SEILKFZTLVMHRR-UHFFFAOYSA-N 2-phosphonooxyethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOP(O)(O)=O SEILKFZTLVMHRR-UHFFFAOYSA-N 0.000 description 1
- ULKFLOVGORAZDI-UHFFFAOYSA-N 3,3-dimethyloxetan-2-one Chemical compound CC1(C)COC1=O ULKFLOVGORAZDI-UHFFFAOYSA-N 0.000 description 1
- WSQZNZLOZXSBHA-UHFFFAOYSA-N 3,8-dioxabicyclo[8.2.2]tetradeca-1(12),10,13-triene-2,9-dione Chemical compound O=C1OCCCCOC(=O)C2=CC=C1C=C2 WSQZNZLOZXSBHA-UHFFFAOYSA-N 0.000 description 1
- YICAEXQYKBMDNH-UHFFFAOYSA-N 3-[bis(3-hydroxypropyl)phosphanyl]propan-1-ol Chemical compound OCCCP(CCCO)CCCO YICAEXQYKBMDNH-UHFFFAOYSA-N 0.000 description 1
- SZTDSGCADFWGKM-UHFFFAOYSA-N 3-[bis(3-hydroxypropyl)phosphoryl]propan-1-ol Chemical compound OCCCP(=O)(CCCO)CCCO SZTDSGCADFWGKM-UHFFFAOYSA-N 0.000 description 1
- MORLYCDUFHDZKO-UHFFFAOYSA-N 3-[hydroxy(phenyl)phosphoryl]propanoic acid Chemical compound OC(=O)CCP(O)(=O)C1=CC=CC=C1 MORLYCDUFHDZKO-UHFFFAOYSA-N 0.000 description 1
- DYIZJUDNMOIZQO-UHFFFAOYSA-N 4,5,6,7-tetrabromo-2-[2-(4,5,6,7-tetrabromo-1,3-dioxoisoindol-2-yl)ethyl]isoindole-1,3-dione Chemical compound O=C1C(C(=C(Br)C(Br)=C2Br)Br)=C2C(=O)N1CCN1C(=O)C2=C(Br)C(Br)=C(Br)C(Br)=C2C1=O DYIZJUDNMOIZQO-UHFFFAOYSA-N 0.000 description 1
- YRHVBTMOZMKPRA-UHFFFAOYSA-N 4-[bis(3-hydroxybutyl)phosphoryl]butan-2-ol Chemical compound CC(O)CCP(=O)(CCC(C)O)CCC(C)O YRHVBTMOZMKPRA-UHFFFAOYSA-N 0.000 description 1
- XKTOUYQJWMIEFI-UHFFFAOYSA-N 4-[bis(4-hydroxybutyl)phosphanyl]butan-1-ol Chemical compound OCCCCP(CCCCO)CCCCO XKTOUYQJWMIEFI-UHFFFAOYSA-N 0.000 description 1
- SFHBJXIEBWOOFA-UHFFFAOYSA-N 5-methyl-3,6-dioxabicyclo[6.2.2]dodeca-1(10),8,11-triene-2,7-dione Chemical compound O=C1OC(C)COC(=O)C2=CC=C1C=C2 SFHBJXIEBWOOFA-UHFFFAOYSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 101000837805 Homo sapiens Testis-expressed protein 44 Proteins 0.000 description 1
- 239000004594 Masterbatch (MB) Substances 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- PHGBTOBVWQJBKT-UHFFFAOYSA-N OC(=O)P(O)=O Chemical compound OC(=O)P(O)=O PHGBTOBVWQJBKT-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 1
- 102100028514 Testis-expressed protein 44 Human genes 0.000 description 1
- QHWKHLYUUZGSCW-UHFFFAOYSA-N Tetrabromophthalic anhydride Chemical compound BrC1=C(Br)C(Br)=C2C(=O)OC(=O)C2=C1Br QHWKHLYUUZGSCW-UHFFFAOYSA-N 0.000 description 1
- GTVWRXDRKAHEAD-UHFFFAOYSA-N Tris(2-ethylhexyl) phosphate Chemical compound CCCCC(CC)COP(=O)(OCC(CC)CCCC)OCC(CC)CCCC GTVWRXDRKAHEAD-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 235000010724 Wisteria floribunda Nutrition 0.000 description 1
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 1
- VFIJBTVGUHVPPW-UHFFFAOYSA-N [Br].C=C Chemical compound [Br].C=C VFIJBTVGUHVPPW-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000002390 adhesive tape Substances 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 125000005210 alkyl ammonium group Chemical group 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 229910000410 antimony oxide Inorganic materials 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 230000003796 beauty Effects 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- APOXBWCRUPJDAC-UHFFFAOYSA-N bis(2,6-dimethylphenyl) hydrogen phosphate Chemical compound CC1=CC=CC(C)=C1OP(O)(=O)OC1=C(C)C=CC=C1C APOXBWCRUPJDAC-UHFFFAOYSA-N 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- WHHGLZMJPXIBIX-UHFFFAOYSA-N decabromodiphenyl ether Chemical compound BrC1=C(Br)C(Br)=C(Br)C(Br)=C1OC1=C(Br)C(Br)=C(Br)C(Br)=C1Br WHHGLZMJPXIBIX-UHFFFAOYSA-N 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- VZEGPPPCKHRYGO-UHFFFAOYSA-N diethoxyphosphorylbenzene Chemical group CCOP(=O)(OCC)C1=CC=CC=C1 VZEGPPPCKHRYGO-UHFFFAOYSA-N 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- BTVWZWFKMIUSGS-UHFFFAOYSA-N dimethylethyleneglycol Natural products CC(C)(O)CO BTVWZWFKMIUSGS-UHFFFAOYSA-N 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 210000000720 eyelash Anatomy 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000007850 fluorescent dye Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- CAYGQBVSOZLICD-UHFFFAOYSA-N hexabromobenzene Chemical compound BrC1=C(Br)C(Br)=C(Br)C(Br)=C1Br CAYGQBVSOZLICD-UHFFFAOYSA-N 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- 238000005453 pelletization Methods 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001230 polyarylate Polymers 0.000 description 1
- 229920006389 polyphenyl polymer Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920002215 polytrimethylene terephthalate Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 239000012756 surface treatment agent Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
- DQWPFSLDHJDLRL-UHFFFAOYSA-N triethyl phosphate Chemical compound CCOP(=O)(OCC)OCC DQWPFSLDHJDLRL-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
- FIQMHBFVRAXMOP-UHFFFAOYSA-N triphenylphosphane oxide Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)(=O)C1=CC=CC=C1 FIQMHBFVRAXMOP-UHFFFAOYSA-N 0.000 description 1
- KOWVWXQNQNCRRS-UHFFFAOYSA-N tris(2,4-dimethylphenyl) phosphate Chemical compound CC1=CC(C)=CC=C1OP(=O)(OC=1C(=CC(C)=CC=1)C)OC1=CC=C(C)C=C1C KOWVWXQNQNCRRS-UHFFFAOYSA-N 0.000 description 1
- QEEHNBQLHFJCOV-UHFFFAOYSA-N tris(2-phenylphenyl) phosphate Chemical compound C=1C=CC=C(C=2C=CC=CC=2)C=1OP(OC=1C(=CC=CC=1)C=1C=CC=CC=1)(=O)OC1=CC=CC=C1C1=CC=CC=C1 QEEHNBQLHFJCOV-UHFFFAOYSA-N 0.000 description 1
- LIPMRGQQBZJCTM-UHFFFAOYSA-N tris(2-propan-2-ylphenyl) phosphate Chemical compound CC(C)C1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C(C)C)OC1=CC=CC=C1C(C)C LIPMRGQQBZJCTM-UHFFFAOYSA-N 0.000 description 1
- BHYQWBKCXBXPKM-UHFFFAOYSA-N tris[3-bromo-2,2-bis(bromomethyl)propyl] phosphate Chemical compound BrCC(CBr)(CBr)COP(=O)(OCC(CBr)(CBr)CBr)OCC(CBr)(CBr)CBr BHYQWBKCXBXPKM-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Artificial Filaments (AREA)
Abstract
Description
本発明は、平滑性、くし通り性、難燃性、耐シャンプー性に優れた難燃性人工頭髪用繊維に関するものである。 The present invention relates to a flame-retardant artificial hair fiber excellent in smoothness, combing property, flame retardancy and shampoo resistance.
かつらやヘアーウィッグ等に用いる人工毛髪として種々の合成繊維のフィラメントが用いられている。そして、このような人工毛髪用の合成繊維フィラメントの材料としては、塩化ビニル、モダアクリル、ポリエステル、ナイロン等が広く用いられている。ポリエステル繊維、ポリプロピレン繊維、ポリアミド繊維等は、そのまま人工毛髪として使用すると難燃性が不十分である。 Various synthetic fiber filaments are used as artificial hair used in wigs, hair wigs, and the like. As materials for synthetic fiber filaments for artificial hair, vinyl chloride, modacrylic, polyester, nylon, and the like are widely used. Polyester fiber, polypropylene fiber, polyamide fiber and the like are insufficient in flame retardancy when used directly as artificial hair.
これらの合成繊維の難燃性を向上させようとする試みは種々なされており、例えばポリエステル樹脂にリン原子を含有する難燃モノマーを共重合する方法、例えば、リン原子が環員子となっていて熱安定性の良好なリン化合物を共重合する方法(特許文献1)、また、カルボキシホスフィン酸を共重合する方法(特許文献2)、ポリアリレートを含むポリエステルにリン化合物を配合又は共重合する方法(特許文献3)が提案されている。これらの難燃化技術を人工毛髪に適用したものとしては、例えば、リン化合物を共重合したポリエステル繊維が提案されている(特許文献4,5)。 Various attempts have been made to improve the flame retardancy of these synthetic fibers. For example, a method in which a flame retardant monomer containing a phosphorus atom is copolymerized with a polyester resin, for example, a phosphorus atom is a ring member. And a method of copolymerizing a phosphorus compound having good thermal stability (Patent Document 1), a method of copolymerizing carboxyphosphinic acid (Patent Document 2), and a compound containing or blending a phosphorus compound with a polyester containing polyarylate A method (Patent Document 3) has been proposed. For example, a polyester fiber copolymerized with a phosphorus compound has been proposed as an application of these flame retardant techniques to artificial hair (Patent Documents 4 and 5).
人工毛髪として使用する場合、柔軟性、平滑性等を付与するために、一般的に、種々のシリコーン系仕上剤が使用されている。例えば、柔軟性、防しわ性、弾力と圧縮回復性を付与するため、ジメチルポリシロキサン、メチル水素ポリシロキサン、両末端水酸基ジメチルポリシロキサン、ビニル基含有オルガノポリシロキサン、エポキシ基含有オルガノポリシロキサン、アミノ基含有オルガノポリシロキサン、エステル基含有オルガノポリシロキサン、ポリオキシアルキレン含有オルガノポリシロキサン等である。また、アルコキシシランの組合せ及び/またはポリアクリルアミド樹脂や触媒からなる処理剤等が知られていた。 When used as artificial hair, various silicone finishes are generally used to impart flexibility, smoothness and the like. For example, dimethylpolysiloxane, methylhydrogen polysiloxane, hydroxylated dimethylpolysiloxane, vinyl group-containing organopolysiloxane, epoxy group-containing organopolysiloxane, amino, to give flexibility, wrinkle resistance, elasticity and compression recovery Group-containing organopolysiloxane, ester group-containing organopolysiloxane, polyoxyalkylene-containing organopolysiloxane, and the like. Further, a treatment agent comprising a combination of alkoxysilanes and / or a polyacrylamide resin or a catalyst has been known.
例えば、1分子当り少なくとも2個のエポキシ基を含有するオルガノポリシロキサンとアミノ基を含有するオルガノポリシロキサンからなる処理剤(特許文献6)、両末端水酸基オルガノポリシロキサン、1分子中にアミノ基とアルコキシ基を含有するオルガノポリシロキサン、及び/または、その部分加水分解物および縮合物からなる処理剤(特許文献7)による方法が開示されている。 For example, a treating agent (Patent Document 6) comprising an organopolysiloxane containing at least two epoxy groups per molecule and an organopolysiloxane containing amino groups, hydroxyl-terminated organopolysiloxane, amino groups in one molecule A method using a treating agent (Patent Document 7) comprising an organopolysiloxane containing an alkoxy group and / or a partial hydrolyzate and a condensate thereof is disclosed.
また、エポキシ基を含有するオルガノポリシロキサンとアミノアルキルトリアルコキシシランからなる処理剤(特許文献8,9)が、1分子中にアミノ基2個以上を含有する両末端トリオルガノシロキシ基ジオルガノポリシロキサン(特許文献10)が記載されている。その他にも、1分子中に2個以上アミノ基を含有するアミノポリシロキサンとアミノ基、エポキシ基等の反応性基を1個以上含有するアルコキシシランからなる処理剤(特許文献11)による方法が提案されている。 Further, a treating agent comprising an organopolysiloxane containing an epoxy group and an aminoalkyltrialkoxysilane (Patent Documents 8 and 9) is a triorganosiloxy group diorganopolyester having both ends containing two or more amino groups in one molecule. Siloxane (Patent Document 10) is described. In addition, there is a method using a treatment agent (Patent Document 11) comprising an aminopolysiloxane containing two or more amino groups in one molecule and an alkoxysilane containing one or more reactive groups such as amino groups and epoxy groups. Proposed.
しかし、これらのシリコーン含有繊維処理剤を付着した繊維は、平滑性、くし通り等の改善はなされるものの、シリコーン系繊維処理剤自体が易燃性であるため、非難燃性合成繊維は易燃性を助長され、難燃性合成繊維に関しても難燃性が著しく低下してしまうという課題が残されたままであった。
難燃性熱可塑性樹脂組成物から形成される繊維の難燃性の低下を軽減し、平滑性、くし通り性、耐シャンプー性に優れた人工毛髪用繊維を提供する。 Provided is a fiber for artificial hair, which reduces a decrease in flame retardancy of a fiber formed from a flame retardant thermoplastic resin composition and is excellent in smoothness, combing resistance and shampoo resistance.
本発明者は上記課題を克服すべく鋭意検討を重ねた結果、難燃性ポリエステル系樹脂組成物から形成される繊維に、脂肪族または芳香族ポリエステルセグメントおよびポリエーテルセグメントを含むランダムまたはブロック共重合体からなる繊維処理剤を付着することにより、平滑性、くし通り性を付与でき、難燃性の低下が軽減された難燃性人工毛髪用繊維が得られ、シャンプーなど洗浄した場倍にもその特性を維持できることを見出した。 As a result of intensive studies to overcome the above problems, the present inventor has found that the fibers formed from the flame-retardant polyester resin composition contain random or block co-polymers containing aliphatic or aromatic polyester segments and polyether segments. By attaching a fiber treatment agent composed of coalescence, it is possible to give smoothness and combing properties, and to obtain a fiber for flame retardant artificial hair with reduced flame retardancy. Even when washed with shampoo etc. It was found that the characteristics can be maintained.
すなわち、本発明は、
難燃性ポリエステル系樹脂組成物(A)からなる組成物から形成される繊維に、脂肪族または芳香族(ポリ)エステルセグメントおよび(ポリ)エーテルセグメントを含むランダムまたはブロック共重合体からなる繊維処理剤(B)を付着させてなる人工毛髪用繊維であり、難燃性ポリエステル系樹脂組成物(A)から形成される繊維に対し、繊維処理剤(B)の合計付着量が、重量比で0.01〜1%である人工毛髪用繊維であり、好ましくは、難燃性ポリエステル系樹脂組成物(A)が、ポリエステル系樹脂(A1)、難燃剤(A2)および難燃助剤(A3)からなり、それぞれの成分比率が、(A1)、(A2)および(A3)を合わせて100重量%とした場合、ポリエステル樹脂(A1)90〜65重量%、難燃剤(A2)10〜25重量%および難燃助剤(A3)0〜10重量%である人工毛髪用繊維であり、ポリエステル系樹脂(A1)が、ポリアルキレンテレフタレートおよびポリアルキレンテレフタレートを主体とした共重合ポリエステルの1種以上からなるポリエステルであり、難燃剤(A2)が、ホスフェート系化合物、ホスホネート系化合物、ホスフィネート系化合物、ホスフィンオキサイド系化合物、ホスファイト化合物、ホスホナイト系化合物、ホスフィナイト系化合物、ホスフィン系化合物、縮合リン酸エステル化合物、有機環状リン化合物、臭素含有リン酸エステル系難燃剤、臭素化ポリスチレン系難燃剤、臭素化ベンジルアクリレート系難燃剤、臭素化エポキシ系難燃剤、臭素化フェノキシ系難燃剤、臭素化ポリカーボネート系難燃剤、テトラブロモビスフェノールA誘導体、臭素含有トリアジン系化合物および臭素含有イソシアヌル酸系化合物よりなる群から選ばれる少なくとも一種であり、難燃助剤(A3)が、メラミンシアヌレート、三酸化アンチモン、四酸化アンチモン、五酸化アンチモン、アンチモン酸ナトリウム、ホウ酸亜鉛、錫酸亜鉛およびヒドロキシ錫酸亜鉛よりなる群から選ばれる少なくとも一種であり、ポリエステル樹脂組成物(A)の限界酸素指数(LOI)が25以上である人工毛髪用繊維である。さらに好ましくは、繊維処理剤(B)が、下記一般式(1)で表される(ポリ)エステルセグメントおよび下記一般式(2)で表される(ポリ)エーテルセグメントを含むランダムまたはブロック共重合体であり、
That is, the present invention
Fiber treatment comprising a random or block copolymer containing an aliphatic or aromatic (poly) ester segment and a (poly) ether segment on a fiber formed from a composition comprising the flame retardant polyester resin composition (A) It is a fiber for artificial hair formed by adhering the agent (B), and the total amount of the fiber treatment agent (B) attached to the fiber formed from the flame retardant polyester resin composition (A) by weight ratio. It is a fiber for artificial hair that is 0.01 to 1%. Preferably, the flame-retardant polyester resin composition (A) comprises a polyester resin (A1), a flame retardant (A2), and a flame retardant aid (A3). ), And each component ratio is 100% by weight of (A1), (A2) and (A3), polyester resin (A1) 90-65% by weight, flame retardant (A2) 10 5% by weight and flame retardant aid (A3) 0 to 10% by weight of artificial hair fiber, polyester resin (A1) is a type of copolymer polyester mainly composed of polyalkylene terephthalate and polyalkylene terephthalate The polyester comprising the above, the flame retardant (A2) is a phosphate compound, a phosphonate compound, a phosphinate compound, a phosphine oxide compound, a phosphite compound, a phosphonite compound, a phosphinite compound, a phosphine compound, condensed phosphoric acid Ester compound, organic cyclic phosphorus compound, bromine-containing phosphate ester flame retardant, brominated polystyrene flame retardant, brominated benzyl acrylate flame retardant, brominated epoxy flame retardant, brominated phenoxy flame retardant, brominated polycarbonate Flame retardant, Tetra It is at least one selected from the group consisting of a lomobisphenol A derivative, a bromine-containing triazine compound and a bromine-containing isocyanuric acid compound, and the flame retardant aid (A3) is melamine cyanurate, antimony trioxide, antimony tetraoxide, five Artificial oxygen which is at least one selected from the group consisting of antimony oxide, sodium antimonate, zinc borate, zinc stannate and zinc hydroxystannate, and has a limiting oxygen index (LOI) of 25 or more in the polyester resin composition (A) It is a fiber for hair. More preferably, the fiber treatment agent (B) contains a (poly) ester segment represented by the following general formula (1) and a (poly) ether segment represented by the following general formula (2). Coalesced,
(式中、mは2〜4の整数、nは1〜100の整数を示す。) (In the formula, m represents an integer of 2 to 4, and n represents an integer of 1 to 100.)
(式中、R1は水素またはメチル基、pは1〜200の整数を示す。)
繊維処理剤(B)の重量平均分子量が、1000〜30000である人工毛髪用繊維に関する。
(In the formula, R 1 represents hydrogen or a methyl group, and p represents an integer of 1 to 200.)
It is related with the fiber for artificial hair whose weight average molecular weights of a fiber processing agent (B) are 1000-30000.
また、上記人工毛髪用繊維には、アニオン系および/またはカチオン系の帯電防止剤を付着させているのが好ましい。 Moreover, it is preferable that an anionic and / or cationic antistatic agent is attached to the artificial hair fiber.
本発明によると、難燃性熱可塑性樹脂組成物から形成される繊維において、平滑性、くし通り性、難燃性、耐シャンプー性に優れた難燃性人工毛髪用繊維が得られる。 According to the present invention, in a fiber formed from a flame retardant thermoplastic resin composition, a flame retardant artificial hair fiber excellent in smoothness, combing property, flame resistance and shampoo resistance can be obtained.
本発明の人工毛髪用繊維は、難燃性ポリエステル系樹脂組成物(A)から形成される繊維に、脂肪族または芳香族(ポリ)エステルセグメントおよび(ポリ)エーテルセグメントを含むランダムまたはブロック共重合体からなる繊維処理剤(B)を付着させてなる人工毛髪用繊維である。 The fiber for artificial hair of the present invention is a random or block co-polymer containing an aliphatic or aromatic (poly) ester segment and a (poly) ether segment in the fiber formed from the flame-retardant polyester resin composition (A). It is a fiber for artificial hair to which a fiber treatment agent (B) made of coalescence is adhered.
難燃性ポリエステル系樹脂組成物(A)から形成される繊維重量に対し、繊維処理剤(B)の付着量が、重量比で0.01〜1%である人工毛髪用繊維である。 It is a fiber for artificial hair whose adhesion amount of the fiber treatment agent (B) is 0.01 to 1% by weight with respect to the fiber weight formed from the flame retardant polyester resin composition (A).
難燃性ポリエステル系樹脂組成物(A)は、ポリエステル系樹脂(A1)、難燃剤(A2)および難燃助剤(A3)からなり、それぞれの成分比率が、(A1)、(A2)および(A3)を合わせて100重量%とした場合、ポリエステル樹脂(A1)90〜65重量%、難燃剤(A2)10〜25重量%および難燃助剤(A3)0〜10重量%である。 The flame retardant polyester resin composition (A) is composed of a polyester resin (A1), a flame retardant (A2), and a flame retardant aid (A3), and each component ratio is (A1), (A2) and When the total amount of (A3) is 100% by weight, it is 90 to 65% by weight of the polyester resin (A1), 10 to 25% by weight of the flame retardant (A2), and 0 to 10% by weight of the flame retardant aid (A3).
本発明で用いられる難燃性ポリエステル系樹脂組成物(A)は、ポリエステル系樹脂(A1)、難燃剤(A2)および難燃助剤(A3)からなる難燃性ポリエステルであることが、難燃性、繊維物性、人工毛髪としての特性の点から好ましい。 It is difficult for the flame retardant polyester resin composition (A) used in the present invention to be a flame retardant polyester composed of a polyester resin (A1), a flame retardant (A2), and a flame retardant aid (A3). It is preferable from the point of the property as a flammability, a fiber physical property, and artificial hair.
本発明に用いられるポリエステル系樹脂(A1)には特に限定はなく、10〜100dtexの人工毛髪繊維の紡糸に適する樹脂であればよい。ポリエステル系樹脂(A)は、ポリアルキレンテレフタレートまたはポリアルキレンテレフタレートを主体とした共重合ポリエステルの1種以上からなるポリエステルである。ポリアルキレンテレフタレートしては、例えば、ポリエチレンテレフテレート、ポリトリメチレンテレフテレート、ポリブチレンテレフテレートなどが挙げられ、それぞれが単独構成のポリマーである必要はなく、ブレンドポリマーや共重合ポリマーであっても良い。これらのなかでも、耐熱性、繊維物性、入手の容易さ、安価なコストの点から、ポリエチレンテレフタレートが好ましい。 There is no limitation in particular in the polyester-type resin (A1) used for this invention, What is necessary is just a resin suitable for spinning of 10-100 dtex artificial hair fiber. The polyester resin (A) is a polyester composed of at least one of polyalkylene terephthalate or a copolyester mainly composed of polyalkylene terephthalate. Examples of the polyalkylene terephthalate include polyethylene terephthalate, polytrimethylene terephthalate, polybutylene terephthalate, etc., and each does not need to be a single polymer, but can be a blend polymer or copolymer polymer. There may be. Among these, polyethylene terephthalate is preferable from the viewpoint of heat resistance, fiber properties, availability, and low cost.
本発明に用いられる難燃剤(A2)には特に限定はなく、一般的に用いられているリン含有難燃剤、ハロゲン含有難燃剤であれば使用することができる。リン含有難燃剤の具体例としては、例えば、トリメチルホスフェート、トリエチルホスフェート、トリブチルホスフェート、トリ(2−エチルヘキシル)ホスフェート、トリフェニルホスフェート、トリクレジルホスフェート、トリキシレニルホスフェート、トリス(イソプロピルフェニル)ホスフェート、トリス(フェニルフェニル)ホスフェート、トリネフチルホスフェート、クレジルフェニルホスフェート、キシレニルジフェニルホスフェート、トリフェニルホスフィンオキサイド、トリクレジルホスフィンオキサイド、メタンホスホン酸ジフェニル、フェニルホスホン酸ジエチルなどのほか、レゾルシノールポリフェニルホスフェート、レゾルシノールポリ(ジ−2,6−キシリル)ホスフェート、ビスフェノールAポリクレジルホスフェート、ハイドロキノンポリ(2,6−キシリル)ホスフェート、ジエチル−N,N−ビス(2−ヒドロキシエチル)アミノメチルホスホネート、2−メタクリロイルオキシエチルアシッドホスフェート、ジフェニル−2−メタクリロイルオキシエチルホスフェート、トリス(3−ヒドロキシプロピル)ホスフィン、トリス(4−ヒドロキシブチル)ホスフィン、トリス(3−ヒドロキシプロピル)ホスフィンオキシド、トリス(3−ヒドロキシブチル)ホスフィンオキシド、3−(ヒドロキシフェニルホスフィノイル)プロピオン酸などが挙げられる。 There is no limitation in particular in the flame retardant (A2) used for this invention, If it is a phosphorus containing flame retardant generally used and a halogen containing flame retardant, it can be used. Specific examples of the phosphorus-containing flame retardant include, for example, trimethyl phosphate, triethyl phosphate, tributyl phosphate, tri (2-ethylhexyl) phosphate, triphenyl phosphate, tricresyl phosphate, trixylenyl phosphate, tris (isopropylphenyl) phosphate, Tris (phenylphenyl) phosphate, trinephtyl phosphate, cresylphenyl phosphate, xylenyl diphenyl phosphate, triphenylphosphine oxide, tricresylphosphine oxide, methanephosphonic acid diphenyl, phenylphosphonic acid diethyl, and resorcinol polyphenyl Phosphate, resorcinol poly (di-2,6-xylyl) phosphate, bisphenol A polycresyl phosphate Fate, hydroquinone poly (2,6-xylyl) phosphate, diethyl-N, N-bis (2-hydroxyethyl) aminomethylphosphonate, 2-methacryloyloxyethyl acid phosphate, diphenyl-2-methacryloyloxyethyl phosphate, tris (3 -Hydroxypropyl) phosphine, tris (4-hydroxybutyl) phosphine, tris (3-hydroxypropyl) phosphine oxide, tris (3-hydroxybutyl) phosphine oxide, 3- (hydroxyphenylphosphinoyl) propionic acid and the like. .
ハロゲン含有難燃剤の具体例としては、例えば、ペンタブロモトルエン、ヘキサブロモベンゼン、デカブロモジフェニル、デカブロモジフェニルエーテル、ビス(トリブロモフェノキシ)エタン、テトラブロモ無水フタル酸、エチレンビス(テトラブロモフタルイミド)、エチレンビス(ペンタブロモフェニル)、オクタブロモトリメチルフェニルインダン、トリス(トリブロモネオペンチル)ホスフェートなどの臭素含有リン酸エステル類、臭素化ポリスチレン類、臭素化ポリベンジルアクリレート類、臭素化エポキシオリゴマー類、臭素化ポリカーボネートオリゴマー類、テトラブロモビスフェノールA、テトラブロモビスフェノールA−ビス(2,3−ジブロモプロピルエーテル)、テトラブロモビスフェノールA−ビス(アリルエーテル)、テトラブロモビスフェノールA−ビス(ヒドロキシエチルエーテル)、テトラブロモビスフェノールA誘導体、トリス(トリブロモフェノキシ)トリアジンなどの臭素含有トリアジン系化合物、トリス(2,3−ジブロモプロピル)イソシアヌレートなどの臭素含有イソシアヌル酸系化合物などが挙げられる。 Specific examples of the halogen-containing flame retardant include, for example, pentabromotoluene, hexabromobenzene, decabromodiphenyl, decabromodiphenyl ether, bis (tribromophenoxy) ethane, tetrabromophthalic anhydride, ethylenebis (tetrabromophthalimide), ethylene Bromine-containing phosphate esters such as bis (pentabromophenyl), octabromotrimethylphenylindane, tris (tribromoneopentyl) phosphate, brominated polystyrenes, brominated polybenzyl acrylates, brominated epoxy oligomers, brominated Polycarbonate oligomers, tetrabromobisphenol A, tetrabromobisphenol A-bis (2,3-dibromopropyl ether), tetrabromobisphenol A-bis (allylamine) ), Tetrabromobisphenol A-bis (hydroxyethyl ether), tetrabromobisphenol A derivatives, bromine-containing triazine compounds such as tris (tribromophenoxy) triazine, bromine such as tris (2,3-dibromopropyl) isocyanurate Examples thereof include isocyanuric acid-based compounds.
これらのうちでは、耐熱性、繊維物性の低下抑制の点から、融点が100℃以上、さらには160℃以上の難燃剤が好ましく、難燃性の強さの点から、ハロゲン系難燃剤を使用するのが好ましい。 Among these, a flame retardant having a melting point of 100 ° C. or higher, more preferably 160 ° C. or higher is preferable from the viewpoint of heat resistance and fiber property deterioration suppression, and a halogen-based flame retardant is used from the viewpoint of flame retardant strength. It is preferable to do this.
ハロゲン系難燃剤の中では、臭素含有リン酸エステル系難燃剤、臭素化ポリスチレン系難燃剤、臭素化ベンジルアクリレート系難燃剤、臭素化ポリカーボネート系難燃剤、臭素化エポキシ系難燃剤、テトラブロモビスフェノールA誘導体、臭素化トリアジン系化合物または臭素含有イソシアヌル酸系化合物が好ましく、さらに、透明性、発色性の点から、臭素含有リン酸エステル系難燃剤、臭素化エポキシ系難燃剤が好ましい。 Among halogen flame retardants, bromine-containing phosphate ester flame retardant, brominated polystyrene flame retardant, brominated benzyl acrylate flame retardant, brominated polycarbonate flame retardant, brominated epoxy flame retardant, tetrabromobisphenol A Derivatives, brominated triazine-based compounds or bromine-containing isocyanuric acid-based compounds are preferable, and brominated phosphate-based flame retardants and brominated epoxy-based flame retardants are more preferable in terms of transparency and color developability.
本発明に用いられる難燃剤(A3)には特に限定はなく、一般的に用いられている難燃
助剤であれば使用することができる。難燃助剤の具体例としては、例えば、メラミンシアヌレート、三酸化アンチモン、四酸化アンチモン、五酸化アンチモン、アンチモン酸ナトリウムなどが挙げられる。これらは、必要に応じて、エポキシ化合物、シラン化合物、イソシアネート化合物、チタネート化合物等で表面処理されてもよい。
The flame retardant (A3) used in the present invention is not particularly limited, and any flame retardant aid that is generally used can be used. Specific examples of the flame retardant aid include, for example, melamine cyanurate, antimony trioxide, antimony tetraoxide, antimony pentoxide, sodium antimonate, and the like. These may be surface-treated with an epoxy compound, a silane compound, an isocyanate compound, a titanate compound or the like, if necessary.
本発明の難燃性ポリエステル系樹脂組成物における、ポリエステル系樹脂(A1)、難燃剤(A2)および難燃助剤の(A3)の成分比率は、(A1)、(A2)および(A3)を合わせて100重量%とした場合、ポリエステル系樹脂(A1)90〜65重量%、難燃剤(A2)10〜25重量%および難燃助剤(A3)0〜10重量%であることが好ましく、(A1)90〜75重量%、(A2)10〜20重量%および(A3)1〜5重量%であることがより好ましく、(A1)85〜80重量%、(A2)12〜15重量%および(A3)3〜5重量%であることがさらに好ましい。ポリエステル系樹脂(A1)が90重量%より多い場合には、難燃剤(A2)および難燃助剤の(A3)の含有量が少なくなるため、十分な難燃性が得られない傾向があり、65重量%より少ない場合には、耐熱性、繊維物性が低下する傾向がある。難燃剤(A2)が10重量%より少ない場合には、難燃性が不十分となる傾向があり、25重量%より多い場合には、耐熱性、繊維物性が低下する傾向がある。難燃助剤(A3)が10重量%より多い場合には、加工安定性、耐ドリップ性、繊維物性、ポリエステル繊維の色相が低下する傾向がある。 In the flame retardant polyester resin composition of the present invention, the component ratio of the polyester resin (A1), the flame retardant (A2) and the flame retardant auxiliary (A3) is (A1), (A2) and (A3). When the total is 100% by weight, it is preferably 90 to 65% by weight of the polyester resin (A1), 10 to 25% by weight of the flame retardant (A2) and 0 to 10% by weight of the flame retardant aid (A3). (A1) 90 to 75% by weight, (A2) 10 to 20% by weight, and (A3) 1 to 5% by weight, more preferably (A1) 85 to 80% by weight, (A2) 12 to 15% by weight. % And (A3) are more preferably 3 to 5% by weight. When the amount of the polyester-based resin (A1) is more than 90% by weight, the flame retardant (A2) and the flame retardant auxiliary (A3) content tend to be low, so that sufficient flame retardancy tends not to be obtained. When the amount is less than 65% by weight, heat resistance and fiber physical properties tend to decrease. When the amount of the flame retardant (A2) is less than 10% by weight, the flame retardancy tends to be insufficient, and when it is more than 25% by weight, the heat resistance and the fiber physical properties tend to decrease. When the amount of the flame retardant aid (A3) is more than 10% by weight, the processing stability, drip resistance, fiber properties, and the hue of the polyester fiber tend to decrease.
本発明の難燃性熱可塑性組成物においては、ポリエステル系樹脂(A1)としては、ポリエチレンテレフタレート、ポリプロピレンテレフタレート、ポリブチレンテレフタレートが、繊維物性、人工毛髪としての特性の点から好ましく、(A2)と(A3)との組合せとしては、縮合リン酸エステル化合物および/または有機環状リン化合物とメラミンシアヌレートとの組合せ、臭素含有リン酸エステル系難燃剤および/または臭素化エポキシ系難燃剤と三酸化アンチモンおよび/またはアンチモン酸ナトリウムとの組合せが難燃性、繊維の色相の点から好ましい。 In the flame-retardant thermoplastic composition of the present invention, as the polyester resin (A1), polyethylene terephthalate, polypropylene terephthalate, and polybutylene terephthalate are preferable from the viewpoint of fiber properties and properties as artificial hair, and (A2) The combination with (A3) includes a combination of a condensed phosphate ester compound and / or an organic cyclic phosphorus compound and melamine cyanurate, a bromine-containing phosphate ester flame retardant and / or a brominated epoxy flame retardant and antimony trioxide. And / or a combination with sodium antimonate is preferable from the viewpoint of flame retardancy and fiber hue.
本発明においては、難燃性ポリエステル系樹脂組成物(A)の限界酸素指数(LOI)は25以上であることが好ましく、28以上であることがさらに好ましい。限界酸素指数(LOI)が25未満になると、十分な難燃性が得られなくなる傾向がある。 In the present invention, the limiting oxygen index (LOI) of the flame retardant polyester resin composition (A) is preferably 25 or more, and more preferably 28 or more. When the limiting oxygen index (LOI) is less than 25, there is a tendency that sufficient flame retardancy cannot be obtained.
本発明においては、難燃性ポリエステル系樹脂組成物から成形される繊維(A)に、脂肪族または芳香族(ポリ)エステルセグメントおよび(ポリ)エーテルセグメントを含むランダムまたはブロック共重合体からなる繊維処理剤(B)を付着させることにより、触感、くし通り、耐シャンプー性を付与することができる。 In the present invention, a fiber made of a random or block copolymer containing an aliphatic or aromatic (poly) ester segment and a (poly) ether segment in the fiber (A) molded from the flame-retardant polyester resin composition By attaching the treatment agent (B), shampoo resistance can be imparted according to the feel and comb.
本発明に用いられる脂肪族または芳香族(ポリ)エステルセグメントおよび(ポリ)エーテルセグメントを含むランダムまたはブロック共重合体からなる繊維処理剤(B)としては、(ポリ)エステルセグメントと(ポリ)エーテルセグメントを含むランダムまたはブロック共重合体から形成された化合物であれば、使用することができる。 The fiber treatment agent (B) comprising a random or block copolymer containing an aliphatic or aromatic (poly) ester segment and (poly) ether segment used in the present invention includes (poly) ester segment and (poly) ether. Any compound formed from a random or block copolymer containing segments can be used.
本発明の繊維処理剤(B)における(ポリ)エステルセグメントの具体例としては、例えば、(ポリ)グリコリド、(ポリ)カプロラクトン、(ポリ)ピバロラクトン、セバシン酸系、アジピン酸系、フタル酸系などの脂肪族(ポリ)エステル類、(ポリ)エチレンテレフタレート、(ポリ)プロピレンテレフタレート、(ポリ)ブチレンテレフタレートなどの一般式(1)で表される芳香族(ポリ)エステル類が挙げられる。これらの中でも、一般式(1)で表される芳香族ポリエステルセグメントを有するものが、ポリエステル繊維との親和性が強く、耐シャンプー性に優れる点から好ましい。 Specific examples of the (poly) ester segment in the fiber treatment agent (B) of the present invention include, for example, (poly) glycolide, (poly) caprolactone, (poly) pivalolactone, sebacic acid, adipic acid, phthalic acid, and the like. And aromatic (poly) esters represented by the general formula (1) such as (poly) ethylene terephthalate, (poly) ethylene terephthalate, (poly) propylene terephthalate, and (poly) butylene terephthalate. Among these, those having an aromatic polyester segment represented by the general formula (1) are preferable from the viewpoint of strong affinity with polyester fibers and excellent shampoo resistance.
本発明の繊維処理剤(B)における(ポリ)エーテルセグメントの具体例としては、例えば、1,4−ブタンジオール、1,6−ヘキサンジオール、ネオペンチルグリコール、1,4−シクロヘキサンジメタノールなどのジオールからなる(ポリ)エーテル類、(ポリ)エチレングリコール系、(ポリ)プロピレングリコール系などの一般式(2)で表される(ポリ)エーテル類やそれらのランダムまたはブロック共重合体が挙げられる。これらの中でも、一般式(2)で表されるポリエーテルセグメントを有するものが、触感、くし通りの点から好ましい。 Specific examples of the (poly) ether segment in the fiber treatment agent (B) of the present invention include, for example, 1,4-butanediol, 1,6-hexanediol, neopentyl glycol, 1,4-cyclohexanedimethanol and the like. Examples include (poly) ethers composed of diols, (poly) ethylene glycol-based, (poly) propylene glycol-based (poly) ethers represented by the general formula (2), and random or block copolymers thereof. . Among these, what has a polyether segment represented by General formula (2) is preferable from a tactile sensation and a comb point.
本発明に用いられる繊維処理剤(B)の重量平均分子量は、1000〜30000が好ましく、2000〜25000がより好ましく、3000〜20000がさらに好ましい。繊維処理剤(B)の重量平均分子量が1000未満では、繊維処理剤の粘性が高くなるため、繊維の平滑性、くし通り性が得られない傾向があり、30000を超えると、高分子量が大きすぎ、繊維との相互作用(親和性)が低下するために、耐シャンプー性が十分に発現されない傾向がある。 1000-30000 are preferable, as for the weight average molecular weight of the fiber processing agent (B) used for this invention, 2000-25000 are more preferable, and 3000-20000 are more preferable. When the weight average molecular weight of the fiber treatment agent (B) is less than 1000, the fiber treatment agent has a high viscosity, and therefore there is a tendency that the smoothness and combing property of the fiber cannot be obtained. In other words, the interaction (affinity) with the fiber is lowered, so that shampoo resistance tends not to be sufficiently exhibited.
本発明の人工毛髪用繊維における、脂肪族または芳香族(ポリ)エステルセグメントおよび(ポリ)エーテルセグメントを含むランダムまたはブロック共重合体からなる繊維処理剤(B)の付着量は、難燃性ポリエステル系樹脂組成物(A)から形成される繊維の重量に対し、重量比で0.01〜1%が好ましく、0.05〜0.6%がより好ましい。脂肪族または芳香族(ポリ)エステルセグメントおよび(ポリ)エーテルセグメントを含むランダムまたはブロック共重合体からなる繊維処理剤(B)の付着量が、0.01%より少ないと、繊維処理剤の効果発現が不十分なため、繊維の平滑性、くし通り性が得られない傾向があり、1%より多いと、繊維処理剤が過剰になり過ぎて、ベタツキ感を生じたり、蓑毛などの加工時のトラブルを生じる場合がある。 The amount of the fiber treatment agent (B) comprising a random or block copolymer containing an aliphatic or aromatic (poly) ester segment and a (poly) ether segment in the artificial hair fiber of the present invention is a flame-retardant polyester. 0.01 to 1% is preferable by weight ratio with respect to the weight of the fiber formed from a resin composition (A), and 0.05 to 0.6% is more preferable. When the amount of the fiber treatment agent (B) comprising a random or block copolymer containing an aliphatic or aromatic (poly) ester segment and a (poly) ether segment is less than 0.01%, the effect of the fiber treatment agent Insufficient expression tends to prevent fiber smoothness and combability from being obtained. When the amount exceeds 1%, the fiber treatment agent becomes excessive, causing a sticky feeling or when processing eyelashes, etc. May cause trouble.
本発明の人工毛髪用繊維においては、さらに、帯電防止性等を付与するために、親水性繊維処理剤を使用することが好ましい。 In the fiber for artificial hair of the present invention, it is preferable to use a hydrophilic fiber treating agent in order to impart antistatic properties and the like.
本発明における親水性繊維処理剤としては、一般的に用いられている親水性繊維処理剤であれば使用することができる。親水性繊維処理剤の具体例としては、例えば、ポリオキシアルキレンアルキルエーテル、ポリオキシアルキレンアルキルエステル、ポリオキシアルキレンアルキルアミン、N,N−ジヒドロキシエチルアルキルアミド、ポリオキシアルキレンアルキルアミド、ポリグリセリン脂肪酸エステル、ポリオキシアルキレンペンタエリスリトールアルキルエステル、ポリオキシアルキレンソルビタン脂肪酸エステル、ポリオキシアルキレン、アルキルアミン塩、アルキルアンモニウム塩、アルキルアラルキルアンモニウム塩、アルキルピリジニウム塩、アルキルピコリニウム塩、アルキルスルホン酸塩、アルキルベンゼンスルホン酸塩、アルキルナフタレンスルホン酸塩、アルキルスルホ脂肪酸エステル塩、アルキル硫酸エステル塩、アルケニル硫酸エステル塩、ポリオキシアルキレンアルキルエーテル硫酸エステル塩、ポリオキシアルキレンアルキルエーテルカルボン酸塩、ポリオキシアルキレンアルケニルエーテル硫酸エステル塩、アルキルリン酸エステル塩、およびイオン性界面活性剤の混合物などが挙げられる。 As the hydrophilic fiber treatment agent in the present invention, any hydrophilic fiber treatment agent that is generally used can be used. Specific examples of the hydrophilic fiber treating agent include, for example, polyoxyalkylene alkyl ether, polyoxyalkylene alkyl ester, polyoxyalkylene alkylamine, N, N-dihydroxyethyl alkylamide, polyoxyalkylene alkylamide, polyglycerin fatty acid ester. , Polyoxyalkylene pentaerythritol alkyl ester, polyoxyalkylene sorbitan fatty acid ester, polyoxyalkylene, alkylamine salt, alkylammonium salt, alkylaralkylammonium salt, alkylpyridinium salt, alkylpicolinium salt, alkylsulfonate, alkylbenzenesulfonic acid Salt, alkyl naphthalene sulfonate, alkyl sulfo fatty acid ester salt, alkyl sulfate ester salt, alkenyl sulfate Ester salts, polyoxyalkylene alkyl ether sulfate, polyoxyalkylene alkyl ether carboxylates, polyoxyalkylene alkenyl ether sulfate, alkyl phosphate salts, and the like mixture of ionic surfactants.
本発明の人工毛髪用繊維は、例えば、(A1)、(A2)および(A3)成分をドラ
イブレンドした後、例えば、種々の一般的な混練機を用いて溶融混練して得られる組成物を、通常の溶融紡糸法で溶融紡糸することにより製造することができる。
The artificial hair fiber of the present invention is obtained by, for example, dry blending the components (A1), (A2) and (A3) and then melt-kneading the composition using various general kneaders. It can be produced by melt spinning by a normal melt spinning method.
樹脂組成物の製造に用いられる前記混練機の例としては、例えば、一軸押出機、二軸押出機、ロール、バンバリーミキサー、ニーダーなどがあげられる。これらのうちでは、二軸押出機が、混練度の調整、操作の簡便性の点から好ましい。 Examples of the kneader used for the production of the resin composition include, for example, a single screw extruder, a twin screw extruder, a roll, a Banbury mixer, and a kneader. Among these, a twin screw extruder is preferable from the viewpoint of adjusting the degree of kneading and ease of operation.
例えば、スクリュー径45mmの二軸押出機を用いて、シリンダ温度を260〜300℃とし、吐出量50〜150kg/hr、スクリュー回転数150〜200rpmで溶融混練し、ダイスよりストランドを引取、水冷した後に、ストランドカッターを用いてペレット化して、本発明の組成物を得ることができる。 For example, using a twin screw extruder with a screw diameter of 45 mm, the cylinder temperature is 260 to 300 ° C., the discharge amount is 50 to 150 kg / hr, the melt is kneaded at a screw rotation speed of 150 to 200 rpm, the strand is taken out from the die, and water-cooled. Later, the composition of the present invention can be obtained by pelletizing with a strand cutter.
本発明の人工毛髪用繊維を、通常の溶融紡糸法で溶融紡糸する場合には、例えば、押出機、ギアポンプ、口金などの温度を270〜310℃とし、溶融紡糸し、紡出糸条を加熱筒に通過させたのち、ガラス転移点以下に冷却し、50〜5000m/分の速度で引き取ることにより紡出糸条が得られる。また、紡出糸条を冷却用の水を入れた水槽で冷却し、繊度のコントロールを行なうことも可能である。加熱筒の温度や長さ、冷却風の温度や吹付量、冷却水槽の温度、冷却時間、引取速度は、吐出量および口金の孔数によって適宜調整することができる。 When the fiber for artificial hair of the present invention is melt-spun by a normal melt-spinning method, for example, the temperature of an extruder, a gear pump, a base, etc. is set at 270 to 310 ° C., melt-spun, and the spun yarn is heated. After passing through the tube, the yarn is cooled below the glass transition point and taken up at a speed of 50 to 5000 m / min to obtain a spun yarn. It is also possible to control the fineness by cooling the spun yarn in a water tank containing cooling water. The temperature and length of the heating cylinder, the temperature and blowing amount of the cooling air, the temperature of the cooling water tank, the cooling time, and the take-up speed can be appropriately adjusted depending on the discharge amount and the number of holes in the die.
得られた紡出糸条は熱延伸されるが、延伸は紡出糸条を一旦巻き取ってから延伸する2工程法および巻き取ることなく連続して延伸する直接紡糸延伸法のいずれの方法によってもよい。熱延伸は、1段延伸法または2段以上の多段延伸法で行なわれる。熱延伸における加熱手段としては、加熱ローラ、ヒートプレート、スチームジェット装置、温水槽などを使用することができ、これらを適宜併用することもできる。 The obtained spun yarn is heat-drawn, and the drawing is performed by any one of a two-step method in which the spun yarn is once wound and then drawn and a direct spin-drawing method in which the drawn yarn is continuously drawn without being wound. Also good. The hot stretching is performed by a one-stage stretching method or a multi-stage stretching method having two or more stages. As a heating means in the heat stretching, a heating roller, a heat plate, a steam jet device, a hot water tank, or the like can be used, and these can be used in combination as appropriate.
本発明のポリエステル系人工毛髪には、必要に応じて、耐熱剤、光安定剤、蛍光剤、酸化防止剤、静電防止剤、顔料、可塑剤、潤滑剤などの各種添加剤を含有させることができる。顔料を含有させることにより、原着繊維を得ることができる。 The polyester-based artificial hair of the present invention may contain various additives such as heat-resistant agents, light stabilizers, fluorescent agents, antioxidants, antistatic agents, pigments, plasticizers, and lubricants as necessary. Can do. By incorporating a pigment, a primary fiber can be obtained.
本発明のポリエステル系人工毛髪が原着されている場合、そのまま使用することができるが、原着されていない場合、通常のポリエステル系繊維と同様の条件で染色することができる。染色に使用される顔料、染料、助剤などとしては、耐候性および難燃性のよいものが好ましい。 When the polyester-based artificial hair of the present invention is priming, it can be used as it is, but when it is not priming, it can be dyed under the same conditions as ordinary polyester-based fibers. As pigments, dyes, auxiliaries and the like used for dyeing, those having good weather resistance and flame retardancy are preferable.
本発明において、難燃性ポリエステル系樹脂組成物(A)から形成される繊維に対して、脂肪族または芳香族(ポリ)エステルセグメントおよび(ポリ)エーテルセグメントを含むランダムまたはブロック共重合体からなる繊維処理剤(B)を付着させる方法は、特に限定はなく、公知の方法により処理することができる。例えば、本発明の繊維処理剤を含む水溶液を調製し、総繊度10万dtexのトウフィラメントを浸漬し、トウ重量に対して含液率20〜30%となるように絞り、所定量(%omf)の繊維処理剤が付着するように溶液を付着させ、熱風乾燥機を用いて130℃にて10分間乾燥させて、繊維処理剤を付着させることができる。また、延伸、熱処理を行ない、引続き、繊維処理剤を含む水溶液に浸漬し、トウ重量に対して含液率20〜30%となるように絞り、所定量(%omf)の繊維処理剤が付着するように溶液を付着させ、乾燥させて繊維処理剤を付着させることができる。また、定量供給装置を用いて、繊維に付着させることもできる。 In the present invention, the fiber formed from the flame retardant polyester resin composition (A) is made of a random or block copolymer containing an aliphatic or aromatic (poly) ester segment and a (poly) ether segment. The method for attaching the fiber treatment agent (B) is not particularly limited, and the fiber treatment agent (B) can be treated by a known method. For example, an aqueous solution containing the fiber treatment agent of the present invention is prepared, a tow filament having a total fineness of 100,000 dtex is immersed, and squeezed so that the liquid content is 20 to 30% with respect to the tow weight, and a predetermined amount (% omf The fiber treatment agent can be adhered so that the fiber treatment agent is attached and dried at 130 ° C. for 10 minutes using a hot air dryer. In addition, stretching and heat treatment are performed, followed by immersion in an aqueous solution containing a fiber treatment agent, squeezing so that the liquid content is 20 to 30% with respect to the tow weight, and a predetermined amount (% omf) of the fiber treatment agent is adhered. The fiber treatment agent can be adhered by allowing the solution to adhere and drying. Moreover, it can also be made to adhere to a fiber using a fixed amount supply apparatus.
本発明のポリエステル系人工毛髪は、美容熱器具(ヘアーアイロン)を用いたカールセ
ット性に優れ、カールの保持性にも優れる。
The polyester-based artificial hair of the present invention is excellent in curl setting using a beauty heat instrument (hair iron) and excellent in curl retention.
また、本発明の人工毛髪は、モダアクリル繊維、ポリ塩化ビニル繊維など、他の人工毛
髪素材と併用してもよいし、人毛と併用してもよい。
The artificial hair of the present invention may be used in combination with other artificial hair materials such as modacrylic fiber and polyvinyl chloride fiber, or may be used in combination with human hair.
つぎに、本発明を実施例に基づいてさらに具体的に説明するが、本発明はこれらに限定
されるものではない。
Next, the present invention will be described more specifically based on examples, but the present invention is not limited thereto.
なお、特性値の測定法は、以下のとおりである。 The characteristic value measurement method is as follows.
(難燃性)
繊度約50dtexのフィラメントを150mmの長さに切り、0.7gを束ね、一方
の端をクランプで挟んでスタンドに固定して垂直に垂らし、有効長120mmの固定した
フィラメントに20mmの炎を3秒間接炎させ、燃焼させて評価した。
−難燃性−
◎:残炎時間が0秒(着火しない)
○:残炎時間が3秒未満
△:残炎時間が3秒以上、10秒未満
×:残炎時間が10秒以上
−限界酸素指数LOI−
16cm/0.25gのフィラメントを秤量し、端を軽く両面テープでまとめ、懸撚器で挟み撚りをかける。十分に撚りがかかったら、試料の真中を二つに折り2本を撚り合わせる。端を粘着テープで止め、全長7cmになるようにする。105℃で60分間前乾燥を行ない、さらにデシケーターで30分以上乾燥する。乾燥したサンプルを所定の酸素濃度に調整し、40秒後8〜12mmに絞った点火器で上部より着火し、着火後点火器を離す。5cm以上燃えるか、3分以上燃え続けた酸素濃度を調べ、同じ条件で試験を3回繰り返し、限界酸素指数(LOI)とする。
(Flame retardance)
A filament with a fineness of about 50 dtex is cut to a length of 150 mm, 0.7 g is bundled, one end is clamped and fixed to a stand and hung vertically, and a 20 mm flame is applied to the fixed filament with an effective length of 120 mm for 3 seconds. Indirect flames were burned and evaluated.
-Flame resistance-
A: After flame time is 0 seconds (no ignition)
○: After-flame time is less than 3 seconds Δ: After-flame time is 3 seconds or more and less than 10 seconds X: After-flame time is 10 seconds or more −Limited oxygen index LOI−
A 16 cm / 0.25 g filament is weighed, and the ends are lightly gathered with double-sided tape, and sandwiched and twisted with a suspender. When the twist is sufficient, fold the middle of the sample in two and twist the two. Stop the end with adhesive tape so that the total length is 7 cm. Pre-drying is performed at 105 ° C. for 60 minutes, and further drying is performed for 30 minutes or more in a desiccator. The dried sample is adjusted to a predetermined oxygen concentration, and after 40 seconds, ignited from the top with an igniter throttled to 8 to 12 mm, and the igniter is released after ignition. The oxygen concentration that burns for 5 cm or more or continues burning for 3 minutes or more is examined, and the test is repeated three times under the same conditions to obtain the limiting oxygen index (LOI).
(くし通り)
長さ30cm、総繊度10万dtexのトウフィラメントに繊維表面処理剤を付着させ
る。処理されたトウフィラメントにくし(デルリン樹脂製)を通し、くしの通り易さを評
価する。
◎:全く抵抗ない(非常に軽い)
○:ほとんど抵抗ない(軽い)
△:若干抵抗がある(重い)
×:かなり抵抗がある、または、途中で引っかかる
(Comb street)
A fiber surface treatment agent is attached to a tow filament having a length of 30 cm and a total fineness of 100,000 dtex. A comb (made by Delrin resin) is passed through the treated tow filament, and the ease of passing the comb is evaluated.
A: No resistance at all (very light)
○: Almost no resistance (light)
Δ: Some resistance (heavy)
×: There is considerable resistance or it gets caught in the middle
(触感)
長さ30cm、総繊度10万dtexのトウフィラメントを手で触り、フィラメント表
面のベタツキ感、すべり触感を評価する。
◎:さらさら感あり
○:ベタツキ感なし
△:若干ベタツキ感がある
×:ベタツキ感がある
(Feel)
A tow filament having a length of 30 cm and a total fineness of 100,000 dtex is touched by hand to evaluate the feeling of stickiness and slip on the filament surface.
◎: There is a smooth feeling ○: There is no stickiness △: There is a little sticky feeling ×: There is a sticky feeling
(耐シャンプー性)
長さ30cm、総繊度10万dtexのトウフィラメントを、市販のリンス等入っていない通常のシャンプー(例えば、サラ:カネボウ(株)製)を加えて5%にした40℃の温水ですすぎ洗いし、自然乾燥する工程を3サイクル行った。洗浄前後の特性変化(触感、くし通り)を評価する(特性保持性)。また、洗浄前後での繊維処理剤の付着量を測定し、耐シャンプー性の尺度とする。
−特性保持性−
◎:特性に全く変化がない
○:ほとんど変化がない
△:若干変化がある
×:変化がある
−繊維処理剤付着量−
以下の式によって、洗浄前後の付着量を算出した。洗浄前後で繊維処理剤の付着量の変化が大きいものは、耐シャンプー性が低いことを示す。
1)(洗浄前の付着量:%omf)=[(繊維処理剤付着後の重量)−(繊維処理剤付着前の重量)]/(繊維処理剤付着前の重量)×100
2)(洗浄後の付着量:%omf)=[(洗浄後の重量)−(繊維処理剤付着前の重量)]/(繊維処理剤付着前の重量)×100。
(Shampoo resistance)
Rinse the tow filament with a length of 30 cm and a total fineness of 100,000 dtex with warm water of 40 ° C to 5% by adding a normal shampoo (such as Sara: Kanebo Co., Ltd.) that does not contain a commercial rinse. The process of natural drying was performed for 3 cycles. Evaluate changes in characteristics before and after cleaning (tactile feel, combing) (characteristic retention). Also, the amount of the fiber treatment agent attached before and after washing is measured and used as a measure of shampoo resistance.
-Property retention-
◎: There is no change in characteristics. ○: There is almost no change. △: There is a slight change.
The adhesion amount before and after cleaning was calculated by the following formula. A thing with a large change of the adhesion amount of a fiber processing agent before and behind washing | cleaning shows that shampoo resistance is low.
1) (Adhesion amount before cleaning:% omf) = [(weight after adhesion of fiber treatment agent) − (weight before adhesion of fiber treatment agent)] / (weight before adhesion of fiber treatment agent) × 100
2) (Adhesion amount after washing:% omf) = [(Weight after washing) − (Weight before adhesion of fiber treatment agent)] / (Weight before adhesion of fiber treatment agent) × 100.
(帯電防止性)
長さ30cm、総繊度10万dtexのトウフィラメントを、室温25℃、湿度40%
の恒温恒湿室に24時間静置した後に、トウフィラメントの最上部を片手に持って垂直に
垂らし、くし(NEW DELRIN COMB No.826)を0.3m/sの速度
でトウフィラメントの上部3cmのところから、トウフィラメント下端まで、30回以上
通過させたときのトウフィラメントの状態を観察する。
◎:変化なし(静電気の帯電がないため、トウが広がらない)
○:数本のフィラメントが外側にはねる
△:静電気で数十本のフィラメントが外側にはねる
×:静電気で全体的に広がる
(Antistatic property)
A tow filament with a length of 30 cm and a total fineness of 100,000 dtex, room temperature 25 ° C., humidity 40%
After standing in a constant temperature and humidity chamber for 24 hours, hold the top of the tow filament in one hand and hang it vertically, and insert a comb (NEW DELRIN COMB No. 826) 3 cm above the tow filament at a speed of 0.3 m / s. From here, the state of the tow filament is observed when it is passed 30 times or more to the lower end of the tow filament.
A: No change (Tow does not spread because there is no static charge)
○: Several filaments spring outward △: Dozens of filaments spring outward due to static electricity ×: Spreads overall due to static electricity
本実施例および比較例において使用した原料は、以下のとおりである。
ポリエステル(A1):
・ポリエチレンテレフタレート、三菱化学(株)製、BK−2180
難燃剤(A2):
・臭素化エポキシ系難燃剤、阪本薬品工業(株)製、SR−T20000
・環状有機リン化合物、三光(株)製、SANKO−BCA
難燃助剤(A3):
・アンチモン酸ナトリウム、日本精鉱(株)製、SA−A
無機微粒子:
・微粒シリカ、富士シリシア化学(株)製、サイリシア310P
顔料:
・顔料マスタバッチ、カーボンブラック20wt%含有、大日精化工業(株)製、PESM22367BLACK
繊維処理剤:
シリコーン系繊維処理剤:
・アミノ変性シリコーン繊維処理剤;丸菱油化(株)製、KWC−B
親水性繊維処理剤:
・カチオン系界面活性剤、松本油脂製薬(株)製、KRE−103
・エチレンオキサイド−プロピレンオキサイド共重合ランダムポリエーテル、松本油脂製薬(株)製、KRE−102
The raw materials used in the examples and comparative examples are as follows.
Polyester (A1):
-Polyethylene terephthalate, manufactured by Mitsubishi Chemical Corporation, BK-2180
Flame retardant (A2):
-Brominated epoxy flame retardant, Sakamoto Pharmaceutical Co., Ltd., SR-T20000
・ Cyclic organophosphorus compound, Sanko Co., Ltd., SANKO-BCA
Flame retardant aid (A3):
・ Sodium antimonate, manufactured by Nippon Seiko Co., Ltd., SA-A
Inorganic fine particles:
・ Fine silica, manufactured by Fuji Silysia Chemical Co., Ltd., Silicia 310P
Pigment:
-Pigment master batch, carbon black 20wt%, manufactured by Dainichi Seika Kogyo Co., Ltd., PESM22367BLACK
Textile treatment agent:
Silicone fiber treatment agent:
・ Amino-modified silicone fiber treatment agent; manufactured by Maruhishi Oil Chemical Co., Ltd., KWC-B
Hydrophilic fiber treatment agent:
・ Cationic surfactant, manufactured by Matsumoto Yushi Seiyaku Co., Ltd., KRE-103
-Ethylene oxide-propylene oxide copolymerized random polyether, manufactured by Matsumoto Yushi Seiyaku Co., Ltd., KRE-102
(製造例1〜3)
表1に示す配合比率の組成物を、水分量100ppm以下に乾燥し、ドライブレンドし、二軸押出機(日本製鋼所(株)製、TEX44)に供給し、シリンダ設定温度280℃で溶融混練し、ペレット化した後に、水分量100ppm以下に乾燥させた。
次いで、溶融紡糸機(シンコーマシナリー(株)製、SV30)を用いてバレル設定温度280℃でノズル径0.5mmの丸断面ノズル孔を有する紡糸口金より溶融ポリマーを吐出し、20℃の冷却風により空冷し、100m/分の速度で巻き取って未延伸糸を得た。得られた未延伸糸に対し、85℃に加熱したヒートロールを用いて4倍に延伸し、200℃に加熱したヒートロールを用いて熱処理を行い、30m/分の速度で巻き取り、単繊維繊度が50dtex前後のポリエステル系繊維(マルチフィラメント)を得た。
(Production Examples 1 to 3)
A composition having a blending ratio shown in Table 1 is dried to a water content of 100 ppm or less, dry blended, supplied to a twin screw extruder (manufactured by Nippon Steel Works, TEX44), and melt kneaded at a cylinder set temperature of 280 ° C. And pelletized, and then dried to a moisture content of 100 ppm or less.
Next, using a melt spinning machine (SV30, manufactured by Shinko Machinery Co., Ltd.), the molten polymer is discharged from a spinneret having a round sectional nozzle hole with a nozzle diameter of 0.5 mm at a barrel set temperature of 280 ° C., and cooling air at 20 ° C. And then wound up at a speed of 100 m / min to obtain an undrawn yarn. The obtained unstretched yarn is stretched 4 times using a heat roll heated to 85 ° C., heat treated using a heat roll heated to 200 ° C., wound at a speed of 30 m / min, and single fiber A polyester fiber (multifilament) having a fineness of about 50 dtex was obtained.
(製造例4〜7)
表2に示す比率でジメチルテレフタレート、エチレングリコール、ポリエチレングリコール、ポリプロピレングリコールをエステル交換缶に仕込み、酢酸カルシウム1水塩0.06部を加えて、窒素ガス雰囲気下で4時間かけて140℃から230℃まで昇温して生成するグリコールを系外に留出させながらエステル交換反応を行なった。続いて、0.5部のトリメチルホスフェートと0.3部の酢酸カルシウム1水塩とを8.5部のエチレングリコール中で、全還流下120℃で60分間反応せしめて得たリン酸ジエステルカルシウム塩の溶液に0.57部の酢酸カルシウム1水塩を溶解させ、三酸化アンチモン0.04部と共に重合缶に移した。次いで、1時間かけて4KPaまで減圧し、同時に1時間かけて230℃から275℃まで昇温した。133Pa以下の減圧下、重合温度275℃で重縮合させて、共重合体を得た。
(Production Examples 4 to 7)
Dimethyl terephthalate, ethylene glycol, polyethylene glycol, and polypropylene glycol were charged into a transesterification can at the ratio shown in Table 2, 0.06 part of calcium acetate monohydrate was added, and the temperature was changed from 140 ° C. to 230 ° C. over 4 hours in a nitrogen gas atmosphere. The ester exchange reaction was carried out while distilling out the glycol generated by raising the temperature to 0 ° C. Subsequently, calcium diester phosphate obtained by reacting 0.5 parts trimethyl phosphate and 0.3 parts calcium acetate monohydrate in 8.5 parts ethylene glycol at 120 ° C. for 60 minutes under total reflux. 0.57 parts of calcium acetate monohydrate was dissolved in the salt solution and transferred to a polymerization can with 0.04 parts of antimony trioxide. Subsequently, the pressure was reduced to 4 KPa over 1 hour, and at the same time, the temperature was raised from 230 ° C. to 275 ° C. over 1 hour. Under a reduced pressure of 133 Pa or less, polycondensation was performed at a polymerization temperature of 275 ° C. to obtain a copolymer.
(製造例8)
表2に示す比率でジメチルテレフタレート、エチレングリコール、トリエチレングリコールをエステル交換缶に仕込み、製造例4〜7と同様にしてエステル交換反応を行なった。続いて、同様にして重合缶に移し、1時間かけて4KPaまで減圧し、同時に1時間かけて230℃から250℃まで昇温した。133Pa以下の減圧下、重合温度250℃で重縮合させて、共重合体を得た。
(Production Example 8)
Dimethyl terephthalate, ethylene glycol, and triethylene glycol were charged into a transesterification can at the ratio shown in Table 2, and a transesterification reaction was performed in the same manner as in Production Examples 4 to 7. Subsequently, it was transferred to a polymerization can in the same manner, and the pressure was reduced to 4 KPa over 1 hour, and at the same time, the temperature was raised from 230 ° C. to 250 ° C. over 1 hour. Under a reduced pressure of 133 Pa or less, polycondensation was performed at a polymerization temperature of 250 ° C. to obtain a copolymer.
(実施例1〜8)
製造例1〜3で得られた繊維を用い、表3に示す繊維処理剤を含む水溶液を調製し、総繊度10万dtexのトウフィラメントを浸漬し、トウ重量に対して含液率20〜30%となるように絞り、表2に示す所定量(%omf)の繊維処理剤が付着するように溶液を付着させ、熱風乾燥機を用いて130℃にて10分間乾燥させた。
(Examples 1-8)
Using the fibers obtained in Production Examples 1 to 3, an aqueous solution containing the fiber treatment agent shown in Table 3 was prepared, and a tow filament having a total fineness of 100,000 dtex was immersed, and the liquid content was 20 to 30 with respect to the tow weight. The solution was attached so that a predetermined amount (% omf) of the fiber treatment agent shown in Table 2 was adhered, and dried at 130 ° C. for 10 minutes using a hot air dryer.
繊維処理剤を付着させたそれぞれの繊維について、難燃性、くし通り、触感、耐シャンプー性、帯電防止性について評価した結果を、表4に示す。 Table 4 shows the results of evaluating the flame retardancy, combing, tactile sensation, shampoo resistance, and antistatic property of each fiber to which the fiber treatment agent was adhered.
(比較例1〜3)
製造例1で得られた繊維を用い、表3に示す繊維処理剤を含む水溶液を調製し、総繊度10万dtexのトウフィラメントを浸漬し、トウ重量に対して含液率20〜30%となるように絞り、表2に示す所定量(%omf)の繊維処理剤が付着するように溶液を付着させ、熱風乾燥機を用いて130℃で10分間乾燥させた。
(Comparative Examples 1-3)
Using the fibers obtained in Production Example 1, prepare an aqueous solution containing the fiber treatment agent shown in Table 3, soak tow filaments with a total fineness of 100,000 dtex, and a liquid content of 20 to 30% with respect to the tow weight. The solution was squeezed so that a predetermined amount (% omf) of the fiber treatment agent shown in Table 2 was adhered, and dried at 130 ° C. for 10 minutes using a hot air dryer.
繊維処理剤を付着させたそれぞれの繊維について、難燃性、くし通り、触感、耐シャンプー性、帯電防止性について評価した結果を、表4に示す。 Table 4 shows the results of evaluating the flame retardancy, combing, tactile sensation, shampoo resistance, and antistatic property of each fiber to which the fiber treatment agent was adhered.
表4に示したように、比較例に対し、実施例では、難燃性の低下が小さく十分な難燃性を示し、くし通り性、触感、耐シャンプー性、帯電防止性にも優れた人工毛髪用繊維が得られることが確認された。したがって、今回の難燃性ポリエステル系樹脂組成物から成形される繊維(A)に、脂肪族または芳香族ポリエステルセグメントおよびポリエーテルセグメントを含むランダムまたはブロック共重合体からなる繊維処理剤(B)を使用した人工毛髪用繊維は、繊維処理剤中にポリエステルセグメントを導入することにより、繊維処理剤と難燃性繊維の親和性、相互作用を高めることにより、シャンプーしても繊維処理剤が除去されにくく、特性を保持することができ、通常のシリコーン系繊維処理剤を使用した場合に比べ、くし通り性、触感、耐シャンプー性、帯電防止性の点において優れることが確認された。 As shown in Table 4, with respect to the comparative example, in the example, the decrease in flame retardancy is small and sufficient flame retardancy is exhibited, and the artificial property is excellent in combing property, touch feeling, shampoo resistance, and antistatic property. It was confirmed that a fiber for hair was obtained. Therefore, the fiber treatment agent (B) comprising a random or block copolymer containing an aliphatic or aromatic polyester segment and a polyether segment is added to the fiber (A) molded from the flame retardant polyester resin composition of this time. The used fiber for artificial hair can be removed even when shampooed by introducing a polyester segment into the fiber treatment agent to increase the affinity and interaction between the fiber treatment agent and the flame retardant fiber. It was difficult to maintain characteristics and was confirmed to be superior in terms of combability, tactile sensation, shampoo resistance, and antistatic properties as compared with the case of using a normal silicone fiber treatment agent.
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JPS63211311A (en) * | 1987-02-23 | 1988-09-02 | 帝人株式会社 | Artificial hair |
JP2000119972A (en) * | 1998-10-12 | 2000-04-25 | Kanegafuchi Chem Ind Co Ltd | Fiber for artificial hair applied with new processing agent and ornament for head |
JP2003221733A (en) * | 2002-01-28 | 2003-08-08 | Kanegafuchi Chem Ind Co Ltd | Flame retardant polyester fiber for artificial hair |
JP2005042234A (en) * | 2003-07-25 | 2005-02-17 | Kaneka Corp | Flame-retardant polyester-based fiber for artificial hair |
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JPS63211311A (en) * | 1987-02-23 | 1988-09-02 | 帝人株式会社 | Artificial hair |
JP2000119972A (en) * | 1998-10-12 | 2000-04-25 | Kanegafuchi Chem Ind Co Ltd | Fiber for artificial hair applied with new processing agent and ornament for head |
JP2003221733A (en) * | 2002-01-28 | 2003-08-08 | Kanegafuchi Chem Ind Co Ltd | Flame retardant polyester fiber for artificial hair |
JP2005042234A (en) * | 2003-07-25 | 2005-02-17 | Kaneka Corp | Flame-retardant polyester-based fiber for artificial hair |
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WO2009150553A2 (en) * | 2008-06-10 | 2009-12-17 | Kimberly-Clark Worldwide, Inc. | Fibers formed from aromatic polyester and polyether copolymer |
WO2009150553A3 (en) * | 2008-06-10 | 2010-03-11 | Kimberly-Clark Worldwide, Inc. | Fibers formed from aromatic polyester and polyether copolymer |
US8841386B2 (en) | 2008-06-10 | 2014-09-23 | Kimberly-Clark Worldwide, Inc. | Fibers formed from aromatic polyester and polyether copolymer |
US9163336B2 (en) | 2008-06-10 | 2015-10-20 | Kimberly-Clark Worldwide, Inc. | Fibers formed from aromatic polyester and polyether copolymer |
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