JP7014662B2 - Friction-proof composite fibers, fabrics and clothing - Google Patents
Friction-proof composite fibers, fabrics and clothing Download PDFInfo
- Publication number
- JP7014662B2 JP7014662B2 JP2018067502A JP2018067502A JP7014662B2 JP 7014662 B2 JP7014662 B2 JP 7014662B2 JP 2018067502 A JP2018067502 A JP 2018067502A JP 2018067502 A JP2018067502 A JP 2018067502A JP 7014662 B2 JP7014662 B2 JP 7014662B2
- Authority
- JP
- Japan
- Prior art keywords
- sea
- friction
- component
- island
- resin
- 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.)
- Active
Links
- 239000000835 fiber Substances 0.000 title claims description 84
- 239000002131 composite material Substances 0.000 title claims description 52
- 239000004744 fabric Substances 0.000 title claims description 23
- 239000011347 resin Substances 0.000 claims description 73
- 229920005989 resin Polymers 0.000 claims description 73
- 230000000844 anti-bacterial effect Effects 0.000 claims description 55
- 239000002781 deodorant agent Substances 0.000 claims description 38
- 238000002844 melting Methods 0.000 claims description 36
- 230000008018 melting Effects 0.000 claims description 36
- 239000010954 inorganic particle Substances 0.000 claims description 27
- 239000004952 Polyamide Substances 0.000 claims description 23
- 229920002647 polyamide Polymers 0.000 claims description 23
- 239000000956 alloy Substances 0.000 claims description 19
- 229910045601 alloy Inorganic materials 0.000 claims description 19
- 229920001903 high density polyethylene Polymers 0.000 claims description 15
- 239000004700 high-density polyethylene Substances 0.000 claims description 15
- 229920006149 polyester-amide block copolymer Polymers 0.000 claims description 14
- 229920001684 low density polyethylene Polymers 0.000 claims description 11
- 239000004702 low-density polyethylene Substances 0.000 claims description 11
- 229920000092 linear low density polyethylene Polymers 0.000 claims description 8
- 239000004707 linear low-density polyethylene Substances 0.000 claims description 8
- PTFCDOFLOPIGGS-UHFFFAOYSA-N Zinc dication Chemical compound [Zn+2] PTFCDOFLOPIGGS-UHFFFAOYSA-N 0.000 claims description 4
- 150000002500 ions Chemical class 0.000 claims description 4
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 claims description 3
- 229910001431 copper ion Inorganic materials 0.000 claims description 3
- FOIXSVOLVBLSDH-UHFFFAOYSA-N Silver ion Chemical group [Ag+] FOIXSVOLVBLSDH-UHFFFAOYSA-N 0.000 claims 1
- 239000000306 component Substances 0.000 description 117
- 238000000034 method Methods 0.000 description 24
- 239000008188 pellet Substances 0.000 description 14
- 229920000728 polyester Polymers 0.000 description 14
- 238000009987 spinning Methods 0.000 description 13
- -1 silver ions Chemical class 0.000 description 11
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 10
- 239000011342 resin composition Substances 0.000 description 10
- 238000001125 extrusion Methods 0.000 description 9
- 229910052709 silver Inorganic materials 0.000 description 9
- 239000004332 silver Substances 0.000 description 9
- 229920001577 copolymer Polymers 0.000 description 8
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 7
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 6
- 239000005977 Ethylene Substances 0.000 description 6
- 229910021536 Zeolite Inorganic materials 0.000 description 6
- 239000003242 anti bacterial agent Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 238000009940 knitting Methods 0.000 description 6
- 239000010457 zeolite Substances 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 239000004594 Masterbatch (MB) Substances 0.000 description 4
- 229920002292 Nylon 6 Polymers 0.000 description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- 235000010724 Wisteria floribunda Nutrition 0.000 description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 4
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 4
- 229910000166 zirconium phosphate Inorganic materials 0.000 description 4
- LEHFSLREWWMLPU-UHFFFAOYSA-B zirconium(4+);tetraphosphate Chemical compound [Zr+4].[Zr+4].[Zr+4].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LEHFSLREWWMLPU-UHFFFAOYSA-B 0.000 description 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 230000001771 impaired effect Effects 0.000 description 3
- 150000002484 inorganic compounds Chemical class 0.000 description 3
- 229910010272 inorganic material Inorganic materials 0.000 description 3
- 238000004898 kneading Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- JUWGUJSXVOBPHP-UHFFFAOYSA-B titanium(4+);tetraphosphate Chemical compound [Ti+4].[Ti+4].[Ti+4].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O JUWGUJSXVOBPHP-UHFFFAOYSA-B 0.000 description 3
- 239000002759 woven fabric Substances 0.000 description 3
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 229920002302 Nylon 6,6 Polymers 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000001361 adipic acid Substances 0.000 description 2
- 235000011037 adipic acid Nutrition 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 229910052797 bismuth Inorganic materials 0.000 description 2
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 2
- 229910052810 boron oxide Inorganic materials 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 238000012258 culturing Methods 0.000 description 2
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 description 2
- 150000002009 diols Chemical class 0.000 description 2
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 2
- 238000000691 measurement method Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 229910001961 silver nitrate Inorganic materials 0.000 description 2
- NDVLTYZPCACLMA-UHFFFAOYSA-N silver oxide Chemical compound [O-2].[Ag+].[Ag+] NDVLTYZPCACLMA-UHFFFAOYSA-N 0.000 description 2
- KKCBUQHMOMHUOY-UHFFFAOYSA-N sodium oxide Chemical compound [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 2
- 229910001948 sodium oxide Inorganic materials 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 230000035900 sweating Effects 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- 229910052726 zirconium Inorganic materials 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 239000004716 Ethylene/acrylic acid copolymer Substances 0.000 description 1
- 229920010126 Linear Low Density Polyethylene (LLDPE) Polymers 0.000 description 1
- 229920000305 Nylon 6,10 Polymers 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- ORLQHILJRHBSAY-UHFFFAOYSA-N [1-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1(CO)CCCCC1 ORLQHILJRHBSAY-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003463 adsorbent Substances 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- 235000011010 calcium phosphates Nutrition 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- IQBJFLXHQFMQRP-UHFFFAOYSA-K calcium;zinc;phosphate Chemical compound [Ca+2].[Zn+2].[O-]P([O-])([O-])=O IQBJFLXHQFMQRP-UHFFFAOYSA-K 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000008358 core component Substances 0.000 description 1
- 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 1
- 150000004985 diamines Chemical class 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 229910000388 diammonium phosphate Inorganic materials 0.000 description 1
- 235000019838 diammonium phosphate Nutrition 0.000 description 1
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 description 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
- 229920006242 ethylene acrylic acid copolymer Polymers 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 229910001701 hydrotalcite Inorganic materials 0.000 description 1
- 229960001545 hydrotalcite Drugs 0.000 description 1
- 229910052588 hydroxylapatite Inorganic materials 0.000 description 1
- 229910001410 inorganic ion Inorganic materials 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 description 1
- 229910052808 lithium carbonate Inorganic materials 0.000 description 1
- 238000004020 luminiscence type Methods 0.000 description 1
- 229920001912 maleic anhydride grafted polyethylene Polymers 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000006224 matting agent Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229940117841 methacrylic acid copolymer Drugs 0.000 description 1
- 229920003145 methacrylic acid copolymer Polymers 0.000 description 1
- RTWNYYOXLSILQN-UHFFFAOYSA-N methanediamine Chemical compound NCN RTWNYYOXLSILQN-UHFFFAOYSA-N 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- KYTZHLUVELPASH-UHFFFAOYSA-N naphthalene-1,2-dicarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 KYTZHLUVELPASH-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- XYJRXVWERLGGKC-UHFFFAOYSA-D pentacalcium;hydroxide;triphosphate Chemical compound [OH-].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O XYJRXVWERLGGKC-UHFFFAOYSA-D 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000004445 quantitative analysis Methods 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 238000007151 ring opening polymerisation reaction Methods 0.000 description 1
- 210000002374 sebum Anatomy 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 229910001923 silver oxide Inorganic materials 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
Images
Landscapes
- Multicomponent Fibers (AREA)
- Woven Fabrics (AREA)
Description
本発明は、体育館等での転倒やスライディング時などに、床と布帛との間で生じる摩擦熱によって布帛が溶融することを防止する摩擦防複合融繊維、それを用いた布帛および衣料品に関する。 The present invention relates to a friction-proof composite melt fiber that prevents the fabric from melting due to frictional heat generated between the floor and the fabric during a fall or sliding in a gymnasium or the like, and a fabric and clothing using the same.
ポリエステル繊維は、その優れた力学的特性および化学的特性から、スポーツ衣料分野に数多く利用されている。しかし、ポリエステル等の合成繊維は、綿やレーヨンなどの天然系繊維と異なり、体育館等での転倒やスライディング時、床と布帛との間で生じる摩擦熱によって布帛が溶融し、布帛に穴が開いてしまう欠点を有する。また特にスポーツ衣料分野においては多くの発汗を伴う状況下で使用されるため、汗に含まれる乳酸、尿素などの老廃物や汗をかいた状態で衣服と肌が擦れ合うことで繊維に付着した皮脂などが衣服表面で細菌類により分解されることで悪臭を発することがある。 Polyester fibers are widely used in the field of sports clothing due to their excellent mechanical and chemical properties. However, unlike natural fibers such as cotton and rayon, synthetic fibers such as polyester melt the fabric due to the frictional heat generated between the floor and the fabric when it falls or slides in a gymnasium, etc., and holes are opened in the fabric. It has the drawback of being lost. Also, especially in the field of sports clothing, since it is used in situations involving a lot of sweating, waste products such as lactic acid and urea contained in sweat and sebum attached to fibers due to rubbing between clothes and skin while sweating. Etc. may give off a foul odor when they are decomposed by bacteria on the surface of clothes.
このような問題を解決するため、上述の摩擦熱により布帛が溶融することを防止する方法としては、例えば、特許文献1や2では、鞘成分樹脂よりも融点が低い樹脂成分を芯部に配した繊維とすることで、摩擦熱で鞘部が溶融する温度に上昇する前に芯部が溶解し、その際の吸熱により繊維全体の溶融を防ぐ方法が提案されている。また特許文献3では、鞘成分に用いる樹脂に、鞘成分よりも融点が低い低融点成分を分散させた海島型アロイを芯部に配し、芯部を鞘成分にて薄皮で覆った繊維を用いることにより、より効果的に摩擦熱による溶融を防ぐことが提案されている。
In order to solve such a problem, as a method for preventing the fabric from melting due to the above-mentioned frictional heat, for example, in
また、繊維に抗菌防臭性を与える方法として、例えば、繊維表面に抗菌剤成分としての銀を担持した二酸化チタン成分を吸尽させる方法(特許文献4)、4級化アンモニウム塩を繊維表面に後加工して付着させる方法(特許文献5)、繊維中に抗菌剤を練り込む方法(特許文献6)等が開示されている。 Further, as a method of imparting antibacterial and deodorant properties to the fiber, for example, a method of absorbing the titanium dioxide component carrying silver as an antibacterial agent component on the fiber surface (Patent Document 4), and then applying a quaternized ammonium salt to the fiber surface. A method of processing and adhering (Patent Document 5), a method of kneading an antibacterial agent into fibers (Patent Document 6), and the like are disclosed.
しかしながら、昨今、スポーツ分野の衣料品においても、多種多様な機能を求められているにも拘わらず、摩擦防融性と抗菌防臭性を兼ね備えた繊維についての提案はなかった。 However, in recent years, even in clothing in the sports field, there has been no proposal for a fiber having both friction-proof and antibacterial and deodorant properties, despite the demand for a wide variety of functions.
そこで、本発明は、抗菌防臭性と摩擦防融性を同時に満足する、抗菌防臭性を有する摩擦防融複合繊維、それからなる布帛および衣料品を得ることを目的とする。 Therefore, an object of the present invention is to obtain a friction-proof composite fiber having antibacterial and deodorant properties, which satisfies both antibacterial and deodorant properties and friction-proof properties at the same time, and a cloth and clothing made of the same.
上記目的を達成するため、本発明は、海成分と島成分とからなり、島成分は海成分を構成する樹脂よりも30℃以上低融点である樹脂を含む樹脂からなる海島型複合繊維であって、海成分は銀イオン、亜鉛イオンおよび銅イオンの群から選択される1以上のイオンを放出する無機粒子を含有する抗菌防臭機能を有する摩擦防融複合繊維をその第一の要旨とする。 In order to achieve the above object, the present invention is a sea-island type composite fiber composed of a sea component and an island component, and the island component is a resin containing a resin having a melting point of 30 ° C. or higher lower than that of the resin constituting the sea component. The first gist of the sea component is a friction-proof composite fiber having an antibacterial and deodorant function, which contains inorganic particles that emit one or more ions selected from the group of silver ions, zinc ions, and copper ions.
また、上記摩擦防融複合繊維において、無機粒子が、水溶性ガラス、リン酸ジルコニウムおよびゼオライトの群から選択される少なくとも1種のものであることをその第二の要旨とする。 The second gist of the friction-proof composite fiber is that the inorganic particles are at least one selected from the group of water-soluble glass, zirconium phosphate and zeolite.
更に、上記摩擦防融複合繊維において、海成分が、ポリエステルまたはポリアミドからなり、島成分が、高密度ポリエチレン、低密度ポリエチレンおよび直鎖低密度ポリエチレンの群から選択される1以上の樹脂を含むものであることを第三の要旨とする。 Further, in the friction-proof composite fiber, the sea component is made of polyester or polyamide, and the island component contains one or more resins selected from the group of high-density polyethylene, low-density polyethylene and linear low-density polyethylene. That is the third point.
上記摩擦防融複合繊維において、島成分は、ポリエステルまたはポリアミドの少なくともいずれか1種の樹脂と、高密度ポリエチレン、低密度ポリエチレンおよび直鎖低密度ポリエチレンの群から選択される1以上の樹脂とを含む、海相と島相からなる海島型アロイ樹脂であることを第四の要旨とする。 In the friction-proof composite fiber, the island component comprises at least one resin of polyester or polyamide and one or more resins selected from the group of high-density polyethylene, low-density polyethylene and linear low-density polyethylene. The fourth gist is that it is a sea-island type alloy resin consisting of a sea phase and an island phase.
また、上記摩擦防融複合繊維を20質量%以上含む布帛を第五の要旨とし、当該布帛を含む衣料品を第六の要旨とする。 The fifth gist is a cloth containing 20% by mass or more of the friction-proof composite fiber, and the sixth gist is a woven fabric containing the cloth.
本発明の摩擦防融複合繊維によれば、摩擦防融性が高く、かつ抗菌防臭性を有する布帛や衣料品を提供することができる。 According to the friction-proof composite fiber of the present invention, it is possible to provide a cloth or clothing having high friction-proof property and antibacterial and deodorant property.
以下、本発明を詳細に説明する。
本発明の摩擦防融複合繊維は、海成分と島成分とからなる海島型複合繊維である。
本発明の摩擦防融複合繊維の海成分を構成する樹脂は、繊維形成性樹脂であれば、特に限定するものではないが、例えば、ポリエステル、ポリアミドが好適に挙げられる。
Hereinafter, the present invention will be described in detail.
The friction-proof composite fiber of the present invention is a sea-island type composite fiber composed of a sea component and an island component.
The resin constituting the sea component of the friction-proof composite fiber of the present invention is not particularly limited as long as it is a fiber-forming resin, and examples thereof include polyester and polyamide.
本発明におけるポリエステルは、ジカルボン酸またはそのエステル形成性誘導体と、ジオールまたはそのエステル形成性誘導体から合成される樹脂である。このようなポリエステルとしては、ポリエチレンテレフタレート、ポリブチレンテレフタレート、ポリプロピレンテレフタレート等が挙げられる。 The polyester in the present invention is a resin synthesized from a dicarboxylic acid or an ester-forming derivative thereof and a diol or an ester-forming derivative thereof. Examples of such polyesters include polyethylene terephthalate, polybutylene terephthalate, polypropylene terephthalate and the like.
また、これらのポリエステルには、本発明の目的が損なわれない範囲であれば、他の成分が共重合されていてもよい。具体的には、共重合成分としては、ジカルボン酸成分では、イソフタル酸、ナフタレンジカルボン酸、4、4-ジフェニルジカルボン酸、アジピン酸、セバシン酸およびそのエステル形成性誘導体等やスルホネート基含有イソフタル酸成分等の官能基を有する成分が挙げられる。また、ジオール成分としてはジエチレングリコール、ヘキサメチレングリコール、ネオペンチルグリコール、シクロヘキサンジメタノール等が挙げられる。また、ポリエチレングリコール、ポリプロピレングリコール等のポリオキシアルキレングリコールも挙げられる。共重合量としては、構成する繰り返し単位あたり10モル%以内が好ましく、5モル%以内がより好ましい。 Further, other components may be copolymerized with these polyesters as long as the object of the present invention is not impaired. Specifically, as the copolymerization component, the dicarboxylic acid component includes isophthalic acid, naphthalenedicarboxylic acid, 4,4-diphenyldicarboxylic acid, adipic acid, sebacic acid and its ester-forming derivative, and the sulfonate group-containing isophthalic acid component. Examples thereof include components having a functional group such as. Examples of the diol component include diethylene glycol, hexamethylene glycol, neopentyl glycol, cyclohexanedimethanol and the like. Further, polyoxyalkylene glycols such as polyethylene glycol and polypropylene glycol can also be mentioned. The copolymerization amount is preferably 10 mol% or less, more preferably 5 mol% or less, per constituent repeating unit.
更に、これらポリエステルには、目的を阻害しない範囲において、つや消し剤や着色剤、耐熱安定剤、紫外線吸収剤等の添加剤を含有していてもよい。
本発明におけるポリエステルの粘度は特に制限されるものではなく、通常のポリエステル繊維に利用されている極限粘度[IV]のポリエステルを使用することができる。紡糸性および繊維の力学的強度の点から、例えばポリエチレンテレフタレートであれば、極限粘度[IV]は0.4~1.5であることが好ましく、極限粘度[IV]は0.55~1.0であることがより好ましい。
Further, these polyesters may contain additives such as a matte agent, a colorant, a heat-resistant stabilizer, and an ultraviolet absorber as long as the purpose is not impaired.
The viscosity of the polyester in the present invention is not particularly limited, and a polyester having an extreme viscosity [IV] used for ordinary polyester fibers can be used. From the viewpoint of spinnability and mechanical strength of the fiber, for example, in the case of polyethylene terephthalate, the ultimate viscosity [IV] is preferably 0.4 to 1.5, and the ultimate viscosity [IV] is 0.55 to 1. It is more preferably 0.
本発明におけるポリアミドとしては、ε-カプロラクタムを開環重合して得たポリアミド6やジアミンとジカルボン酸を縮重合して得る、例えばヘキサメチレンジアミンとアジピン酸を縮重合して得たポリアミド66、ヘキサメチレンジアミンとセバシン酸を縮重合して得たポリアミド610などが好適である。 The polyamide in the present invention includes polyamide 6 obtained by ring-opening polymerization of ε-caprolactam, polyamide 66 obtained by polycondensing diamine and dicarboxylic acid, for example, polyamide 66 obtained by polycondensing hexamethylenediamine and adipic acid, and hexa. Polyamide 610 obtained by polycondensation of methylenediamine and sebacic acid is suitable.
更にこれらのポリアミドには、目的を阻害しない範囲において、つや消し剤や着色剤、耐熱安定剤、紫外線吸収剤等の添加剤を含有していてもよい。
本発明におけるポリアミドの粘度は特に制限されるものではなく、通常のポリアミド繊維に利用されている相対粘度[ηr]のポリアミドを使用することができる。紡糸性および繊維の力学的強度の点から、例えばポリアミド6であれば、相対粘度[ηr]は2.0~3.4であることが好ましく、相対粘度[ηr]が2.4~3.0であることがより好ましい。
Further, these polyamides may contain additives such as a matting agent, a colorant, a heat-resistant stabilizer, and an ultraviolet absorber as long as the purpose is not impaired.
The viscosity of the polyamide in the present invention is not particularly limited, and a polyamide having a relative viscosity [ηr] used for ordinary polyamide fibers can be used. From the viewpoint of spinnability and mechanical strength of the fiber, for example, in the case of polyamide 6, the relative viscosity [ηr] is preferably 2.0 to 3.4, and the relative viscosity [ηr] is 2.4 to 3. It is more preferably 0.
次に本発明の摩擦防融複合繊維の島成分について、詳細に説明する。
島成分は、海成分を構成する樹脂より低融点の樹脂(以下、低融点樹脂とよぶことがある)を含むことが肝要である。
Next, the island component of the friction-proof composite fiber of the present invention will be described in detail.
It is important that the island component contains a resin having a lower melting point than the resin constituting the sea component (hereinafter, may be referred to as a low melting point resin).
低融点樹脂は、海成分を構成する樹脂よりも、30℃以上融点が低いものであり、80℃以上融点が低いものであることが好ましく、100℃以上融点が低いものであることがより好ましい。海成分を構成する樹脂と低融点樹脂の融点差が小さいと摩擦防融効果が小さくなる傾向があり、その融点差が30℃未満であると実質的に摩擦防融効果を示さない。 The low melting point resin has a lower melting point of 30 ° C. or higher, preferably 80 ° C. or higher, and more preferably 100 ° C. or higher than the resin constituting the sea component. .. If the melting point difference between the resin constituting the sea component and the low melting point resin is small, the friction-proofing effect tends to be small, and if the melting point difference is less than 30 ° C., the friction-proofing effect is substantially not exhibited.
低融点樹脂としては、例えば、海成分がポリエステルやポリアミドの場合は、海成分より低融点のポリエステル、ポリアミド、ポリプロピレン、ポリエチレン等が挙げられる。摩擦防融性を良好にする点からは、ポリエチレンであることが好ましく、具体的には、高密度ポリエチレン、低密度ポリエチレンおよび直鎖低密度ポリエチレンが好適に挙げられ、これらの樹脂を単独で用いてもよいし、2以上の混合物として用いてもよい。 Examples of the low melting point resin include polyester, polyamide, polypropylene, polyethylene and the like having a lower melting point than the sea component when the sea component is polyester or polyamide. From the viewpoint of improving friction-proof property, polyethylene is preferable, and specific examples thereof include high-density polyethylene, low-density polyethylene and linear low-density polyethylene, and these resins are used alone. It may be used as a mixture of two or more.
島成分は、低融点樹脂のみから構成されてもよいし、一部に低融点樹脂を含むものであってもよい。 The island component may be composed of only a low melting point resin, or may partially contain a low melting point resin.
島成分は、ポリエステルやポリアミド等の海成分の繊維形成性樹脂と、低融点樹脂とを含む、海相と島相からなる海島型アロイ樹脂であってもよい。 The island component may be a sea-island type alloy resin composed of a sea phase and an island phase, which contains a fiber-forming resin of a sea component such as polyester or polyamide and a low melting point resin.
なお、海成分がポリエステルまたはポリアミドから構成される場合、島成分は、高密度ポリエチレン、低密度ポリエチレンおよび直鎖低密度ポリエチレンの少なくとも1以上の低融点樹脂を含むことが好ましい。 When the sea component is composed of polyester or polyamide, the island component preferably contains at least one low melting point resin of high density polyethylene, low density polyethylene and linear low density polyethylene.
島成分が海島型アロイ樹脂の場合は、海成分と島成分との密着性(親和性)を高め、摩擦防融性を良好とする点からは、島成分が海成分と同種の樹脂と、低融点樹脂とを含む混合物からなる海島型アロイ樹脂であることが好ましい。 When the island component is a sea-island type alloy resin, the island component is the same type of resin as the sea component in terms of improving the adhesion (affinity) between the sea component and the island component and improving the friction-proof property. It is preferably a sea-island type alloy resin composed of a mixture containing a low melting point resin.
島成分が海島型アロイ樹脂の場合の具体的な好適な樹脂の組み合わせとして、ポリエステルまたはポリアミドの少なくともいずれか1種の樹脂と、高密度ポリエチレン、低密度ポリエチレンおよび直鎖低密度ポリエチレンの群から選択される1以上の樹脂とを含むものであることが挙げられる。これらの中でも、ポリエステルまたはポリアミドの少なくともいずれか1種の樹脂が海相、高密度ポリエチレン、低密度ポリエチレンおよび直鎖低密度ポリエチレンの群から選択される1以上の樹脂が島相からなる海島型アロイ樹脂であることが好適である。 A specific suitable resin combination when the island component is a sea-island type alloy resin is selected from the group of at least one resin of polyester or polyamide and a group of high density polyethylene, low density polyethylene and linear low density polyethylene. It is mentioned that it contains one or more resins to be made. Among these, a sea-island type alloy in which at least one resin of polyester or polyamide is selected from the group of sea phase, high-density polyethylene, low-density polyethylene and linear low-density polyethylene, and one or more resins are island phases. It is preferably a resin.
島成分が海島型アロイ樹脂の場合、安定した摩擦防融性効果発現の点から、低融点樹脂は、島成分に対し、5~45質量%であることが好ましく、より好ましくは、10~30質量%である。 When the island component is a sea-island type alloy resin, the low melting point resin is preferably 5 to 45% by mass, more preferably 10 to 30% by mass, based on the island component, from the viewpoint of exhibiting a stable friction-proofing effect. It is mass%.
また、島成分が海島型アロイ樹脂の場合は、相溶化剤を添加して含むものとすることが好ましい。相溶化剤の具体例としては、エチレン/アクリル酸共重合体、エチレン/メタクリル酸共重合体、エチレン/アクリル酸エチル共重合体、エチレン/酢酸ビニル共重合体、エチレン/メタクリル酸グリシジル共重合体、エチレン/酢酸ビニル/メタクリル酸グリシジル共重合体、無水マレイン酸グラフトポリエチレン、アクリル酸グラフトポリエチレン、無水マレイン酸グラフトエチレン/プロピレン共重合体、エチレン/プロピレン-メタクリル酸グラフトグリシジル共重合体、無水マレイン酸グラフトエチレン/プロピレン/1,4-ヘキサジエン共重合体またはアクリル酸グラフトエチレン/酢酸ビニル共重合体などが挙げられる。これらの相溶化剤は1種以上用いることが好ましく、2種以上用いてもよい。
相溶化剤の添加量は、島成分を構成する樹脂全体に対し、0.1~10質量%程度が好ましく、より好ましくは0.2~5質量%である。
When the island component is a sea-island type alloy resin, it is preferably contained by adding a compatibilizer. Specific examples of the compatibilizer include ethylene / acrylic acid copolymer, ethylene / methacrylic acid copolymer, ethylene / ethyl acrylate copolymer, ethylene / vinyl acetate copolymer, and ethylene / glycidyl methacrylate copolymer. , Ethylene / vinyl acetate / glycidyl methacrylate copolymer, maleic anhydride grafted polyethylene, acrylic acid grafted polyethylene, maleic anhydride grafted ethylene / propylene copolymer, ethylene / propylene-methacrylic acid grafted glycidyl copolymer, maleic anhydride Examples thereof include a grafted ethylene / propylene / 1,4-hexadiene copolymer or an acrylate-grafted ethylene / vinyl acetate copolymer. It is preferable to use one or more of these compatibilizers, and two or more of them may be used.
The amount of the compatibilizer added is preferably about 0.1 to 10% by mass, more preferably 0.2 to 5% by mass, based on the total amount of the resin constituting the island component.
次に、本発明の摩擦防融複合繊維は、海成分が銀イオン、亜鉛イオンおよび銅イオンの群から選択される1以上のイオンを放出することが可能な無機粒子を含有する。以下、このような無機粒子を本発明における無機粒子という。本発明における無機粒子を含有すると、抗菌防臭効果を有するものとなる。 Next, the friction-proof composite fiber of the present invention contains inorganic particles in which the sea component can emit one or more ions selected from the group of silver ions, zinc ions and copper ions. Hereinafter, such inorganic particles are referred to as inorganic particles in the present invention. When the inorganic particles in the present invention are contained, it has an antibacterial and deodorant effect.
本発明における無機粒子としては、例えば、銀、銅、亜鉛、ビスマス、コバルト、ニッケルなどの抗菌性金属を担持した種々の無機化合物が好適に挙げられる。
抗菌性金属を担持する無機化合物(担持体)としては、例えば、以下の(1)、(2)、(3)に示すものが好適に挙げられる。
(1)ゼオライト、リン酸ジルコニウム、ヒドロキシアパタイト、リン酸チタン、チタン酸カリウム、含水酸化ビスマス、含水酸化アンチモン、含水酸化ジルコニウム、ハイドロタルサイト、リン酸カルシウム、リン酸亜鉛カルシウム,ケイ酸カルシウムなどの無機イオン交換体
(2)酸化チタン、活性炭、活性アルミナなどの無機吸着体
(3)シリカ系ガラス、水溶性ガラスまたはシリカゲルなどの無機媒体(無定形ガラス状物質)
これらのなかでも、銀単体、銀と銅または銀と亜鉛を、水溶性ガラス、リン酸ジルコニウム、リン酸チタンおよびゼオライトから選択される少なくとも1種の無機化合物に担持させた無機粒子であることが好ましい。
本発明の摩擦防融複合繊維は、これらの本発明における無機粒子を、単体で用いても、2以上組み合わせて用いてもよい。
Preferable examples of the inorganic particles in the present invention include various inorganic compounds carrying antibacterial metals such as silver, copper, zinc, bismuth, cobalt and nickel.
As the inorganic compound (supporter) that supports the antibacterial metal, for example, those shown in the following (1), (2), and (3) are preferably mentioned.
(1) Inorganic ions such as zeolite, zirconium phosphate, hydroxyapatite, titanium phosphate, potassium titanate, bismuth-containing hydroxide, antimony-containing hydroxide, zirconium-containing zirconium, hydrotalcite, calcium phosphate, calcium zinc phosphate, calcium silicate, etc. Exchanger (2) Inorganic adsorbent such as titanium oxide, activated carbon, active alumina (3) Inorganic medium such as silica-based glass, water-soluble glass or silica gel (atypical glassy substance)
Among these, it is an inorganic particle in which silver alone, silver and copper or silver and zinc are supported on at least one inorganic compound selected from water-soluble glass, zirconium phosphate, titanium phosphate and zeolite. preferable.
The friction-proof composite fiber of the present invention may use these inorganic particles of the present invention alone or in combination of two or more.
以下、本発明における無機粒子を得る方法について例示する。
担持体がゼオライトの場合、例えば、特開昭59-133235号公報に示されているようにゼオライト微粒子を硝酸銀水溶液で処理してイオン交換反応を行い、ゼオライトに銀を担持させることにより本発明における無機粒子を得ることができる。また市販の製品としては、例えば、シナネンゼオミック社製「ゼオミック(登録商標)(商品名)」として入手できる。
担持体がリン酸ジルコニウムやリン酸チタンの場合、例えば、特開平3-83905号公報に開示されているように炭酸リチウム、リン酸水素二アンモニウムおよび酸化ジルコニウム、または酸化チタンを所定量混合し、1300℃で焼結して得た化合物を微粉砕した後、硝酸銀水溶液で処理して、本発明における無機粒子を得ることができる。市販の製品としては、例えば、東亞合成社製「ノバロン(登録商標)(商品名)」として入手できる。
担持体が水溶性ガラスの場合、例えば、特開平3-124810号公報に開示されているように所定量の酸化銀、酸化ホウ素、シリカおよび酸化ナトリウムを溶融ガラス化し、微粉砕して得た銀イオンを放出する本発明における無機粒子を得たり、特開平7-257938号公報に開示されているように所定量の酸化亜鉛、酸化ホウ素および酸化ナトリウムを1000~1300℃で溶解ガラス化し、微粉砕して得た亜鉛イオンを放出する本発明における無機粒子を得ることができる。市販の製品としては、例えば、石塚硝子社製「イオンピュア(登録商標)(商品名)」として入手できる。
また、市販の富士ケミカル社製の各種抗菌剤を本発明における無機粒子として用いることができる。更に、富士ケミカル社製の各種抗菌剤をポリエステルやポリアミド中に高濃度で分散させている「バクテキラー(登録商標)マスターバッチ(商品名)」であれば、本発明における無機粒子を含有する本発明の摩擦防融複合繊維を容易に得ることができる。
Hereinafter, the method for obtaining the inorganic particles in the present invention will be illustrated.
When the carrier is zeolite, for example, as shown in Japanese Patent Application Laid-Open No. 59-133235, the zeolite fine particles are treated with an aqueous solution of silver nitrate to carry out an ion exchange reaction, whereby silver is supported on the zeolite in the present invention. Inorganic particles can be obtained. As a commercially available product, for example, it can be obtained as "Zeomic (registered trademark) (trade name) " manufactured by Sinanen Zeomic.
When the carrier is zirconium phosphate or titanium phosphate, for example, lithium carbonate, diammonium hydrogen phosphate and zirconium oxide, or titanium oxide are mixed in a predetermined amount as disclosed in JP-A-3-83905. The compound obtained by sintering at 1300 ° C. is finely pulverized and then treated with an aqueous solution of silver nitrate to obtain the inorganic particles of the present invention. As a commercially available product, for example, it can be obtained as "Novalon (registered trademark) (trade name)" manufactured by Toagosei Co., Ltd.
When the carrier is water-soluble glass, for example, as disclosed in Japanese Patent Application Laid-Open No. 3-124810, a predetermined amount of silver oxide, boron oxide, silica and sodium oxide are melt vitrified and finely pulverized to obtain silver. Inorganic particles in the present invention that emit ions can be obtained, or a predetermined amount of zinc oxide, boron oxide and sodium oxide are melted and vitrified at 1000 to 1300 ° C. and finely pulverized as disclosed in JP-A-7-257938. The inorganic particles in the present invention that release the zinc ions thus obtained can be obtained. As a commercially available product, for example, it can be obtained as "Aeon Pure (registered trademark) (trade name)" manufactured by Ishizuka Glass Co., Ltd.
Further, various commercially available antibacterial agents manufactured by Fuji Chemical Co., Ltd. can be used as the inorganic particles in the present invention. Further, if it is a "Bactekiller (registered trademark) masterbatch (trade name)" in which various antibacterial agents manufactured by Fuji Chemical Co., Ltd. are dispersed in polyester or polyamide at a high concentration, the present invention contains the inorganic particles in the present invention. The friction-proof composite fiber of the above can be easily obtained.
本発明の摩擦溶融複合繊維は、このような本発明における無機粒子を海成分に含有することにより抗菌防臭性を有する繊維となる。 The friction-melt composite fiber of the present invention becomes a fiber having antibacterial and deodorant properties by containing such inorganic particles in the present invention in the sea component.
次に、本発明の摩擦防融複合繊維の断面形状について説明する。
本発明の摩擦防融複合繊維は、上述のような海成分と、島成分とからなる海島型複合繊維である。本発明において、海島型複合繊維は、1以上の島成分と、1以上の海成分を複合してなる繊維である。
図1~図4は、本発明の摩擦防融複合繊維の長手方向に垂直な切断面の形状の例である。
図1、図3は、海成分の数が1、島成分の数が1の海島型複合繊維の断面である。
図2、図4は、海成分の数が1、島成分の数が19の海島型複合繊維の断面である。図2、図4の海島型複合繊維の島成分は、中心に1個、中心の島成分の外周を均等に1例に囲んで6個、その外周を均等に1列に囲んで12個の合計19個配されている。
なお、本発明における海島型複合繊維の海成分および島成分の数は1以上であれば、特に制限されるものではないが、口金作製の容易さから、61島以下が好ましく、37島以下がより好ましく、19島以下が最も好ましい。
海成分と、島成分の好適な比率(断面積比率)としては、島成分に低融点樹脂のみを用いる場合は、島成分:海成分比率が、5:95~50:50が好ましく、より好ましくは10:90~30:70である。また、島成分に海島型アロイ樹脂を用いる場合は、島成分:海成分比率が、20:80~70:30の範囲が好ましく、より好ましくは、30:70~50:50である。この範囲であると、紡糸性も良好であり、本発明の効果も奏しやすい。
Next, the cross-sectional shape of the friction-proof composite fiber of the present invention will be described.
The friction-proof composite fiber of the present invention is a sea-island type composite fiber composed of the above-mentioned sea component and an island component. In the present invention, the sea-island type composite fiber is a fiber obtained by combining one or more island components and one or more sea components.
1 to 4 are examples of the shape of the cut surface perpendicular to the longitudinal direction of the friction-proof composite fiber of the present invention.
1 and 3 are cross sections of a sea-island type composite fiber having 1 sea component and 1 island component.
2 and 4 are cross sections of a sea-island type composite fiber having 1 sea component and 19 island components. The island components of the sea-island type composite fiber shown in FIGS. 2 and 4 are 1 in the center, 6 in which the outer circumference of the central island component is evenly surrounded by one example, and 12 in which the outer circumference is evenly surrounded in a row. A total of 19 pieces are distributed.
The number of sea components and island components of the sea-island type composite fiber in the present invention is not particularly limited as long as it is 1 or more. More preferably, 19 islands or less is most preferable.
As a preferable ratio (cross-sectional area ratio) between the sea component and the island component, when only a low melting point resin is used for the island component, the island component: sea component ratio is preferably 5:95 to 50:50, which is more preferable. Is from 10:90 to 30:70. When a sea-island type alloy resin is used as the island component, the island component: sea component ratio is preferably in the range of 20:80 to 70:30, and more preferably 30:70 to 50:50. Within this range, the spinnability is good and the effect of the present invention can be easily achieved.
次に、摩擦防融複合繊維の製造方法の好適な例について、説明する。
まず、ポリエステルペレットまたはポリアミドペレット、本発明における無機粒子、低融点樹脂ペレット等を準備する。
Next, a suitable example of a method for producing a friction-proof composite fiber will be described.
First, polyester pellets or polyamide pellets, inorganic particles in the present invention, low melting point resin pellets and the like are prepared.
次に、芯成分を海島型アロイ樹脂とする場合は、海島型アロイ樹脂を製造する。
具体的には、ポリエステルペレットまたはポリアミドペレットと、低融点樹脂ペレットとを予備混合した後、二軸押出混練機にて、ポリエステルまたはポリアミドの融点より10~40℃高く設定して溶融複合混練して、海島型アロイ樹脂を得ることができる。この際、ポリエステルまたはポリアミドペレットと、低融点樹脂ペレットとの混合比率は、95:5~55:45(質量比)の範囲であることが好ましい。より好ましくは90:10~70:30(質量比)の範囲である。海島型アロイ樹脂を製造する際、海島型アロイ樹脂のモルフォロジーを安定化する目的で、相溶化剤を併用することが好ましく、ペレット混合する際に、樹脂ペレット全体に対し、0.1~10質量%程度、添加して用いることが好ましく、より好ましい添加量は0.2~5質量%である。
Next, when the core component is a sea-island type alloy resin, the sea-island type alloy resin is manufactured.
Specifically, after premixing the polyester pellets or polyamide pellets with the low melting point resin pellets, the melt composite kneading is performed at a temperature of 10 to 40 ° C. higher than the melting point of the polyester or polyamide in a twin-screw extrusion kneader. , A sea-island type alloy resin can be obtained. At this time, the mixing ratio of the polyester or polyamide pellets and the low melting point resin pellets is preferably in the range of 95: 5 to 55:45 (mass ratio). More preferably, it is in the range of 90:10 to 70:30 (mass ratio). When producing a sea-island type alloy resin, it is preferable to use a compatibilizer in combination for the purpose of stabilizing the morphology of the sea-island type alloy resin, and when the pellets are mixed, 0.1 to 10 mass with respect to the entire resin pellets. It is preferable to add and use about%, and a more preferable amount of addition is 0.2 to 5% by mass.
次に、海成分として、予め本発明における無機粒子を含む樹脂組成物を紡糸に供する場合、海成分のベース樹脂に本発明における無機粒子を含む樹脂組成物を準備する。具体的には、二軸押出混練機の第1フィード口から、海成分を構成するベース樹脂を供給し、溶解したところへサイドフィーダーを用いて、本発明における無機粒子を、所定比率になるように第2フィード口より供給し複合化させて樹脂組成物を得る方法、予め海成分のベース樹脂を粉末化し所定量の無機粒子を予備混合したものを二軸押出混練機または単軸の押出機で溶融混合して樹脂組成物を得る方法等により、製造して得ることができる。また、市販の各種抗菌剤をポリエステルやポリアミド中に高濃度で分散させているマスターバッチ(例えば、富士ケミカル社製の「バクテキラー(登録商標)マスターバッチ(商品名)」)をベース樹脂に希釈混合して樹脂組成物として用いることもできる。 Next, when the resin composition containing the inorganic particles of the present invention is previously subjected to spinning as the sea component, the resin composition containing the inorganic particles of the present invention is prepared as the base resin of the sea component. Specifically, the base resin constituting the sea component is supplied from the first feed port of the twin-screw extruder and kneader, and the inorganic particles in the present invention are adjusted to a predetermined ratio by using a side feeder to the melted portion. A method of obtaining a resin composition by supplying it from the second feed port and compounding it, a twin-screw extruder or a single-screw extruder in which a base resin of sea components is powdered in advance and a predetermined amount of inorganic particles are premixed. It can be produced and obtained by a method such as a method of obtaining a resin composition by melting and mixing with. In addition, a masterbatch in which various commercially available antibacterial agents are dispersed in polyester or polyamide at a high concentration (for example, "Bactekiller (registered trademark) masterbatch (trade name)" manufactured by Fuji Chemical Co., Ltd.) is diluted and mixed with the base resin. It can also be used as a resin composition.
低融点樹脂または海島型アロイ樹脂、本発明における無機粒子を含む樹脂組成物を、押出機により、それぞれの樹脂を溶解し、所謂スピンパック内で、低融点樹脂または海島型アロイ樹脂を島部、本発明における無機粒子を含む樹脂組成物を海部の形状に合して、紡糸口金から吐出する。吐出された糸条を、所望に応じて延伸して、本発明の摩擦防融複合繊維を得ることができる。なお、海部に本発明における無機粒子を含む樹脂組成物を用いず、海成分を構成する樹脂と本発明における無機粒子を紡糸時にブレンドして繊維を製造してもよい。
紡糸延伸方法としては、(1)一旦、吐出された糸条を未延伸糸として巻き取った後、延伸機で延伸して延伸糸を得るコンベンショナル法、(2)吐出された糸条を、一旦巻き取ることなく、第1ローラーと第2ローラーとの間で延伸しながら巻き取るスピンドロー法、(3)吐出された糸条を3000~4500m/分程度で部分延伸糸として巻き取った後、仮撚機で延伸仮撚するPOY-DTY法等、適宜、選択できる。
A resin composition containing a low melting point resin or a sea island type alloy resin and the inorganic particles in the present invention is melted by an extruder, and the low melting point resin or the sea island type alloy resin is applied to the island in a so-called spin pack. The resin composition containing the inorganic particles in the present invention is matched to the shape of the sea portion and discharged from the spinneret. The discharged yarn can be stretched as desired to obtain the friction-proof composite fiber of the present invention. The fiber may be produced by blending the resin constituting the sea component and the inorganic particles of the present invention at the time of spinning without using the resin composition containing the inorganic particles of the present invention in the sea portion.
As the spinning and drawing method, (1) a conventional method in which the discharged yarn is once wound as an undrawn yarn and then drawn by a drawing machine to obtain a drawn yarn, and (2) the discharged yarn is once. Spin-draw method in which the yarn is wound while being drawn between the first roller and the second roller without winding. (3) The discharged yarn is wound as a partially drawn yarn at about 3000 to 4500 m / min. The POY-DTY method of stretching and false twisting with a false twisting machine can be appropriately selected.
なお、海成分と島成分の繊維断面積比率(長手方向に垂直な面の面積比率)は、海島型アロイ樹脂を用いる場合は、紡糸性を良好とする点から、島成分:海成分の比率が、20:80~70:30の範囲とすることが好ましく、より好ましくは、30:70~50:50である。また島成分に低融点樹脂のみを用いる場合、島成分:海成分の比率が、5:95~50:50の範囲が好ましく、より好ましくは、10:90~30:70である。 The fiber cross-sectional area ratio of the sea component and the island component (the area ratio of the surface perpendicular to the longitudinal direction) is the ratio of the island component: the sea component from the viewpoint of improving the spinnability when the sea island type alloy resin is used. However, it is preferably in the range of 20:80 to 70:30, and more preferably 30:70 to 50:50. When only the low melting point resin is used as the island component, the ratio of the island component: the sea component is preferably in the range of 5:95 to 50:50, more preferably 10:90 to 30:70.
このようにして得られた本発明の摩擦防融複合繊維を、一部または全部に用いて、製編織して、布帛を得ることができる。 The friction-proof composite fiber of the present invention thus obtained can be partially or wholly used for knitting and weaving to obtain a fabric.
本発明の布帛は、摩擦防融性、抗菌防臭性の点から、本発明の摩擦防融複合繊維を20質量%以上含むことが好ましく、より好ましくは、33質量%以上、更に好ましくは50質量%であり、最も好ましくは全量用いることである。 From the viewpoint of friction-proof and antibacterial deodorant properties, the fabric of the present invention preferably contains the friction-proof composite fiber of the present invention in an amount of 20% by mass or more, more preferably 33% by mass or more, still more preferably 50% by mass. %, And most preferably the whole amount is used.
本発明の布帛の形態としては、織物、編物、不織布等の繊維構造物が好適に挙げられる。
織物の組織としては、平織、朱子織等が好適に挙げられ、編物の組織としては、丸編み(緯編み)、トリコット(経編)等が好適に挙げられる。
Suitable examples of the form of the fabric of the present invention include fiber structures such as woven fabrics, knitted fabrics, and non-woven fabrics.
As the structure of the woven fabric, plain weave, satin weave and the like are preferably mentioned, and as the structure of the knitted fabric, circular knitting (weft knitting), tricot (warp knitting) and the like are preferably mentioned.
本発明の摩擦防融複合繊維を含む布帛は、優れた摩擦防融性と抗菌防臭性を備えたものであるため、ジャージ、バレーボールやハンドボールのゲームシャツ、スポーツ用ウォームウェアー等の衣料品に好適に用いることができる。 The fabric containing the friction-proof composite fiber of the present invention has excellent friction-proof properties and antibacterial deodorant properties, and is therefore suitable for clothing such as jerseys, volleyball and handball game shirts, and sports warm wear. Can be used for.
以下に実施例を挙げて本発明を具体的に説明する。なお、本発明は以下に述べる実施例に限定されるものではない。 Hereinafter, the present invention will be specifically described with reference to examples. The present invention is not limited to the examples described below.
樹脂の粘度の測定方法は以下の通りとした。
(極限粘度[IV]の測定方法)
所定量のポリエステルをフェノール/1,1,2,2-テトラクロロエタン=60/40(質量比)の混合溶媒に溶解し、ウベローデ粘度計を用い20℃に設定した株式会社柴山科学機器製作所製自動粘度測定装置SS-270LCにて常法で測定した。
The method for measuring the viscosity of the resin was as follows.
(Measuring method of ultimate viscosity [IV])
A predetermined amount of polyester was dissolved in a mixed solvent of phenol / 1,1,2,2-tetrachloroethane = 60/40 (mass ratio), and the temperature was set to 20 ° C. using an Ubbelohde viscometer. It was measured by a conventional method with a viscosity measuring device SS-270LC.
(相対粘度[ηr]の測定方法)
所定量のポリアミドを96質量%の硫酸に溶解し、ウベローデ粘度計を用い20℃に設定した株式会社柴山科学機器製作所製自動粘度測定装置SS-270LCにて常法で測定した。
(Measurement method of relative viscosity [ηr])
A predetermined amount of polyamide was dissolved in 96% by mass of sulfuric acid, and the viscosity was measured by a conventional method using an automatic viscosity measuring device SS-270LC manufactured by Shibayama Kagaku Kikai Seisakusho Co., Ltd., which was set at 20 ° C. using a Ubbelohde viscometer.
本発明における評価方法は、以下の通りとした。
A)摩擦防融性
繊維を英光産業製筒編み機型番:NCR-EWを用い24ゲージで編地化し、布地を2枚重ね合せてJIS L1056(B法)に準拠したローター型摩擦溶融試験機を用い摩擦防融性を評価した。ローターに布地を10秒間押し付けた後の布地状態を次の4段階で分別した。
◎:ほぼ変化が認められないもの
○:擦過痕が認められるもの
△:部分的に溶融が認められるもの
×:溶融により穴あきが認められたもの
B)抗菌防臭性
得られた繊維を試験片とし、JIS L1902-2015「繊維製品の抗菌性試験方法及び抗菌効果」の菌液吸収法に準拠して試験を行い、附属書D「発光測定法による定量法」を用いて抗菌活性値を求めた。18時間培養後の抗菌活性値が2.2以上の場合を○と分類し、抗菌防臭性を有すると判定した。18時間培養後の抗菌活性値が2.2未満の場合を×と分類し、抗菌防臭性が無いと判定した。
The evaluation method in the present invention is as follows.
A) Friction-proof fiber is knitted with a 24-gauge knitting machine using Eiko Sangyo's tube knitting machine model number: NCR-EW, and two fabrics are overlapped to form a rotor type friction melting tester conforming to JIS L1056 (B method). The friction-proof property used was evaluated. The state of the cloth after pressing the cloth against the rotor for 10 seconds was classified in the following four stages.
⊚: Almost no change ○: Scratch marks are observed △: Partially melted ×: Perforated due to melting B) Antibacterial and deodorant The obtained fiber is a test piece. Then, the test was conducted in accordance with the bacterial solution absorption method of JIS L1902-2015 "Antibacterial test method and antibacterial effect of textile products", and the antibacterial activity value was obtained using Annex D "Quantitative method by luminescence measurement method". rice field. When the antibacterial activity value after culturing for 18 hours was 2.2 or more, it was classified as ◯ and judged to have antibacterial and deodorant properties. When the antibacterial activity value after culturing for 18 hours was less than 2.2, it was classified as x, and it was judged that there was no antibacterial deodorant property.
〔参考例1〕
島成分として、IVが0.67のホモポリエステルに、MFRが7g/10分の高密度ポリエチレン(HDPE)を80:20の割合で混合し、更に混合ペレットに対し0.3質量%の相溶化剤(住友化学製ボンドファースト(商品名))を更に混合したものを280℃に温度設定した二軸押出混練機で溶融混練したものを用い、海成分として、IVが0.67のホモポリエステルに東亞合成社製ノバロン(登録商標)AG300(商品名)を1質量%の割合となるように280℃に温度設定した二軸押出混練機で溶融混練したものを用い、海成分と島成分の比率(面積比)50:50にて、図1の断面形状(海成分の数:1、島成分の数:1)となるように、紡速3800m/分のスピンドロー法にて紡糸し、84dtex/24fの複合繊維を得た。
得られた繊維を用い、摩擦防融性を評価したところ、擦過痕もほとんど無く、◎の判定であった。更に抗菌防臭性を評価したところ、抗菌活性値が2.4で、抗菌防臭性を有するとの判定であった。
[ Reference Example 1]
As an island component, high-density polyethylene (HDPE) having an MFR of 7 g / 10 min was mixed with a homopolyester having an IV of 0.67 at a ratio of 80:20, and further compatible with 0.3% by mass with respect to the mixed pellets. A mixture of the agent (Sumitomo Chemical's Bond First (trade name)) was melt-kneaded in a twin-screw extrusion kneader set at a temperature of 280 ° C to make a homopolyester with an IV of 0.67 as a sea component. The ratio of sea component and island component was made by melting and kneading Novalon (registered trademark) AG300 (trade name) manufactured by Toa Synthetic Co., Ltd. with a twin-screw extrusion kneader whose temperature was set to 280 ° C so that the ratio was 1% by mass. At a (area ratio) of 50:50, spinning was performed by a spin draw method at a spinning speed of 3800 m / min so as to have the cross-sectional shape of FIG. 1 (number of sea components: 1, number of island components: 1), and 84 dtex. A composite fiber of / 24f was obtained.
When the friction-proof property was evaluated using the obtained fibers, there were almost no scratch marks, and the judgment was ⊚. Further, when the antibacterial and deodorant properties were evaluated, the antibacterial activity value was 2.4, and it was determined that the antibacterial and deodorant properties were obtained.
〔実施例2〕
島成分として、MFRが7g/10分の高密度ポリエチレン(HDPE)を用い、海成分として、IVが0.67のホモポリエステルと富士ケミカル製の可溶性ガラス系抗菌剤を20質量%ポリエステルに複合したバクテキラーマスターバッチとを95:5の割合でチップ混合したものを用い、図4のような島数が19となる口金を用いて、海成分と島成分の比率(面積比)が90:10の割合で、紡速3800m/分のスピンドロー法により紡糸を行い、84dtex/24fの海島型複合繊維を得た。
得られた繊維を用い、摩擦防融性を評価したところ、擦過痕がわずかに認められ、〇の判定であった。更に抗菌防臭性を評価したところ、抗菌活性値が2.3となり、抗菌防臭性を有するとの判定であった。
[Example 2]
High-density polyethylene (HDPE) with an MFR of 7 g / 10 minutes was used as the island component, and a homopolyester with an IV of 0.67 and a soluble glass-based antibacterial agent manufactured by Fuji Chemical were combined with 20% by mass polyester as a sea component. Using a bacteceller masterbatch mixed with chips at a ratio of 95: 5, and using a base with 19 islands as shown in Fig. 4, the ratio (area ratio) of the sea component to the island component is 90:10. Spinning was carried out by a spin draw method at a spinning speed of 3800 m / min to obtain a sea-island type composite fiber having 84 dtex / 24 f.
When the friction-proof property was evaluated using the obtained fiber, a slight scratch mark was observed, and the judgment was 〇. Further, when the antibacterial and deodorant properties were evaluated, the antibacterial activity value was 2.3, and it was determined that the antibacterial and deodorant properties were obtained.
〔参考例3〕
島成分として、MFRが5g/10分の直鎖状低密度ポリエチレン(LLDPE)を用い、海成分として、シナネンゼオミック社のゼオミック(登録商標)を2質量%含有したηrが2.7のポリアミド6を用い、島成分:海成分比率が25:75となるように、図3のような島数が1となる口金を用いて、紡速4200m/分のスピンドロー法にて紡糸し、84dtex/24fの複合繊維を得た。
得られた繊維を用い、摩擦防融性を評価したところ、擦過痕が少し認められ、〇の判定であった。更に抗菌防臭性を評価したところ、抗菌活性値が2.5であり、抗菌防臭性を有するとの判定であった。
[ Reference Example 3]
As an island component, linear low density polyethylene (LLDPE) with an MFR of 5 g / 10 minutes is used, and as a sea component, a polyamide 6 having 2.7 ηr containing 2% by mass of Zeomic (registered trademark) of Sinanen Zeomic. Is spun by the spin draw method at a spinning speed of 4200 m / min using a base having an island number of 1 as shown in FIG. 3 so that the island component: sea component ratio is 25:75, and 84 dtex / A composite fiber of 24f was obtained.
When the friction-proof property was evaluated using the obtained fibers, some scratch marks were observed, and the judgment was ◯. Further, when the antibacterial and deodorant properties were evaluated, the antibacterial activity value was 2.5, and it was determined that the antibacterial and deodorant properties were obtained.
〔参考例4〕
島成分として、MFRが7g/10分の低密度ポリエチレン(LDPE)と、IVが0.67のホモポリエステルとを2:8の割合で混合し、更に相溶化剤としてLDPEとホモポリエステルの合計量に対し0.3質量%の相溶化剤(住友化学製ボンドファースト(商品名))を追加ペレット混合したものを280℃に温度設定した二軸押出混練機で溶融混練した樹脂組成物を用い、海成分として、実施例1で用いたIVが0.67のホモポリエステルに東亞合成社製ノバロン(登録商標)AG300(商品名)を1質量%の割合になるように280℃に温度設定した二軸押出混練機で溶融混練した樹脂組成物を用い、海成分と島成分の比率(面積比)が40:60となるように、図2のような島数が19となる口金を用いて、紡速3800m/分のスピンドロー法により紡糸し、84dtex/24fの海島型複合繊維を得た。
得られた繊維を用い、摩擦防融性を評価したところ、擦過痕もほとんど無く、◎の判定であった。更に抗菌防臭性を評価したところ、抗菌活性値が2.4であり、抗菌防臭性を有するとの判定であった。
[ Reference Example 4]
As an island component, low-density polyethylene (LDPE) with an MFR of 7 g / 10 min and homopolyester with an IV of 0.67 are mixed at a ratio of 2: 8, and the total amount of LDPE and homopolyester as a compatibilizer. Using a resin composition in which 0.3% by mass of a compatibilizer (Bond First (trade name) manufactured by Sumitomo Chemical Co., Ltd.) was added and mixed in pellets and melt-kneaded in a twin-screw extrusion kneader set at a temperature of 280 ° C. As a sea component, the temperature of Novalon (registered trademark) AG300 (trade name) manufactured by Toa Synthetic Co., Ltd. was set to 280 ° C. so as to be 1% by mass in the homopolyester having IV of 0.67 used in Example 1. Using a resin composition melt-kneaded with a shaft extrusion kneader, using a base with 19 islands as shown in FIG. 2 so that the ratio (area ratio) of the sea component to the island component is 40:60. Spinning was performed by a spin draw method at a spinning speed of 3800 m / min to obtain a sea-island type composite fiber of 84 dtex / 24 f.
When the friction-proof property was evaluated using the obtained fibers, there were almost no scratch marks, and the judgment was ⊚. Further, when the antibacterial and deodorant properties were evaluated, the antibacterial activity value was 2.4, and it was determined that the antibacterial and deodorant properties were obtained.
〔参考例5〕
島成分として、ηrが2.7のポリアミド6にMFRが7g/10分の高密度ポリエチレン(HDPE)を80:20の割合で混合し、更に混合ペレットに対し0.3質量%の相溶化剤(住友化学製ボンドファースト(商品名))を更に混合したものを250℃に温度設定した二軸押出混練機で溶融混練したものを用い、海成分として、IV が0.67のホモポリエステルに東亞合成社製ノバロン(登録商標)AG300(商品名)を1質量%の割合となるように280℃に温度設定した二軸押出混練機で溶融混練したものを用い、海成分と島成分の比率(面積比)50:50にて、図1の断面形状(海成分の数:1、島成分の数:1)となるように、紡速4000m/分のスピンドロー法にて紡糸し、84dtex/24fの複合繊維を得た。
得られた繊維を用い、摩擦防融性を評価したところ、擦過痕もほとんど無く、◎の判定であった。更に抗菌防臭性を評価したところ、抗菌活性値が2.4で、抗菌防臭性を有するとの判定であった。
[ Reference Example 5]
As an island component, high-density polyethylene (HDPE) having an MFR of 7 g / 10 min was mixed with polyamide 6 having a ηr of 2.7 at a ratio of 80:20, and a compatibilizer of 0.3% by mass with respect to the mixed pellets. (Sumitomo Chemical's Bond First (trade name)) was further mixed and melt-kneaded in a twin-screw extrusion kneader set at a temperature of 250 ° C. As a sea component, a homopolyester with an IV of 0.67 was added to Toa. Using a twin-screw extrusion kneader in which the temperature of Novalon (registered trademark) AG300 (trade name) manufactured by Synthetic Co., Ltd. was set to 280 ° C. so that the ratio was 1% by mass, the ratio of sea component and island component was used. Spinned by a spin draw method at a spinning speed of 4000 m / min so as to have the cross-sectional shape of FIG. 1 (number of sea components: 1, number of island components: 1) at 50:50 (area ratio), and 84 dtex / min. A 24f composite fiber was obtained.
When the friction-proof property was evaluated using the obtained fibers, there were almost no scratch marks, and the judgment was ⊚. Further, when the antibacterial and deodorant properties were evaluated, the antibacterial activity value was 2.4, and it was determined that the antibacterial and deodorant properties were obtained.
〔比較例1〕
実施例1で用いたIVが0.67のホモポリエステルを単独でスピンドロー法により紡糸し、84dtex/24fの丸断面繊維を得た。
得られた繊維を用い、摩擦防融性を評価したところ、完全に穴が開き×の判定であった。更に抗菌防臭性を評価したところ、抗菌活性値が0.5であり、抗菌防臭性が無いとの判定であった。
[Comparative Example 1]
The homopolyester having an IV of 0.67 used in Example 1 was independently spun by a spin draw method to obtain a round cross-section fiber of 84 dtex / 24 f.
When the friction-proof property was evaluated using the obtained fiber, the hole was completely opened and the judgment was x. Further, when the antibacterial and deodorant properties were evaluated, the antibacterial activity value was 0.5, and it was determined that there was no antibacterial and deodorant properties.
〔比較例2〕
島成分として、IVが0.67のホモポリエステルを用い、海成分として、実施例1と同様にIVが0.67のホモポリエステルに東亞合成社製ノバロン(登録商標)AG300(商品名)を1質量%の割合となるように280℃に温度設定した二軸押出混練機で溶融混練したものを用い、島成分と海成分の比率(面積比)50:50にて、紡速3800m/分のスピンドロー法にて紡糸し、図1のような島数1、海数1の断面の84dtex/24fの複合繊維を得た。
得られた繊維を用い、摩擦防融性を評価したところ、容易に穴が開き、×の判定であった。更に抗菌防臭性を評価したところ、抗菌活性値が2.4であり、抗菌防臭性を有するとの判定であった。
[Comparative Example 2]
Homopolyester with IV of 0.67 was used as the island component, and Novalon (registered trademark) AG300 (trade name) manufactured by Toagosei Co., Ltd. was added to the homopolyester with IV of 0.67 as the sea component as in Example 1. Using a twin-screw extrusion kneader whose temperature was set to 280 ° C. so as to have a mass% ratio, the melt-kneaded product was used, and the spinning speed was 3800 m / min at a ratio (area ratio) of 50:50 between the island component and the sea component. By spinning by the spin draw method, a composite fiber of 84 dtex / 24f having a cross section of 1 island and 1 sea as shown in FIG. 1 was obtained.
When the friction-proof property was evaluated using the obtained fiber, a hole was easily formed and the judgment was x. Further, when the antibacterial and deodorant properties were evaluated, the antibacterial activity value was 2.4, and it was determined that the antibacterial and deodorant properties were obtained.
〔比較例3〕
海成分に、東亜合成社製のノバロン(登録商標)AG300を用いなかったこと以外は、実施例1と同様にして84dtex/24fの海島型複合繊維を得た。得られた繊維を用い、摩擦防融性を評価したところ、擦過痕もほとんど無く、◎の判定であった。抗菌防臭性を評価したところ、抗菌活性値が0.5で、抗菌防臭性がないとの判定であった。
[Comparative Example 3]
An 84dtex / 24f sea-island type composite fiber was obtained in the same manner as in Example 1 except that Novalon (registered trademark) AG300 manufactured by Toagosei Co., Ltd. was not used as the sea component. When the friction-proof property was evaluated using the obtained fibers, there were almost no scratch marks, and the judgment was ⊚. When the antibacterial and deodorant properties were evaluated, the antibacterial activity value was 0.5, and it was determined that there was no antibacterial and deodorant properties.
〔比較例4〕
島成分として、IVが0.67のホモポリエステルを用い、海成分と島成分の比率(面積比)を50:50とする以外は、実施例3と同様に紡糸し、84dtex/24fの複合繊維を得た。
得られた繊維を用い、摩擦防融性の評価したところ、完全に穴が開き×の判定であった。更に抗菌防臭性を評価したところ、抗菌活性値が2.5であり、〇の判定であった。
[Comparative Example 4]
Homopolyester with IV of 0.67 was used as the island component, and the composite fiber was spun in the same manner as in Example 3 except that the ratio (area ratio) of the sea component to the island component was 50:50. Got
When the friction-proof property was evaluated using the obtained fiber, the hole was completely opened and the judgment was x. Further, when the antibacterial and deodorant properties were evaluated, the antibacterial activity value was 2.5, which was a judgment of 〇.
〔比較例5〕
海成分として実施例1で用いたIVが0.67のホモポリエステルを使用し、島成分として実施例1と同様にIVが0.67のホモポリエステルとMFRが7g/10分のHDPEとを80:20で混合し、混合ペレットに対し0.3質量%の割合となるように相溶化剤(住友化学製ボンドファースト(商品名))と、更に東亞合成社製ノバロン(登録商標)AG300(商品名)を1質量%の割合となるように混合したものを280℃に温度設定した二軸押出混練機で溶融混練したものを用い、後は実施例1と同様に紡糸して84dtex/24fの複合繊維を得た。
得られた繊維を用い、摩擦防融性を評価したところ、擦過痕もほとんど無く、◎の判定であったが、抗菌防臭性を評価したところ、抗菌活性値が0.5で、抗菌防臭性は認められなかった。
[Comparative Example 5]
As the sea component, the homopolyester having an IV of 0.67 used in Example 1 was used, and as the island component, 80 was a homopolyester having an IV of 0.67 and HDPE having an MFR of 7 g / 10 min as in Example 1. Mix at 20 and make a compatibilizer (Bond First (trade name) manufactured by Sumitomo Chemical Co., Ltd.) and Novalon (registered trademark) AG300 (registered trademark) manufactured by Toa Synthetic Co., Ltd. so that the ratio is 0.3% by mass with respect to the mixed pellets. Name) was mixed so as to have a ratio of 1% by mass, melt-kneaded with a twin-screw extrusion kneader set at a temperature of 280 ° C., and then spun in the same manner as in Example 1 to 84dtex / 24f. A composite fiber was obtained.
When the friction-proof property was evaluated using the obtained fiber, there were almost no scratch marks and the judgment was ◎, but when the antibacterial deodorant property was evaluated, the antibacterial activity value was 0.5 and the antibacterial deodorant property. Was not recognized.
実施例、参考例および比較例から得られた繊維と評価について表1に示す。
以上のように、実施例品はいずれも、抗菌防臭性と摩擦防止融性の兼ね備えた繊維となった。 As described above, all of the examples were fibers having both antibacterial deodorant property and anti-friction property.
摩擦防融性を有する衣料品で、かつ抗菌防臭機能を有するスポーツ用途等に適応可能な複合繊維をいる事が出来る。 It is possible to use composite fibers that are friction-proof clothing and are suitable for sports applications having antibacterial and deodorant functions.
1 海成分
2、3 島成分
1
Claims (5)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2018067502A JP7014662B2 (en) | 2018-03-30 | 2018-03-30 | Friction-proof composite fibers, fabrics and clothing |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2018067502A JP7014662B2 (en) | 2018-03-30 | 2018-03-30 | Friction-proof composite fibers, fabrics and clothing |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2019178443A JP2019178443A (en) | 2019-10-17 |
JP2019178443A5 JP2019178443A5 (en) | 2020-08-13 |
JP7014662B2 true JP7014662B2 (en) | 2022-02-01 |
Family
ID=68278024
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2018067502A Active JP7014662B2 (en) | 2018-03-30 | 2018-03-30 | Friction-proof composite fibers, fabrics and clothing |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP7014662B2 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112575408B (en) * | 2020-12-16 | 2023-01-17 | 江苏华峰超纤材料有限公司 | Adventitious island sea-island fiber and preparation method thereof |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2653815B2 (en) | 1988-02-18 | 1997-09-17 | 旭化成工業株式会社 | Fiber material containing metal ions |
JP2000096350A (en) | 1998-07-16 | 2000-04-04 | Mitsubishi Rayon Co Ltd | Sheath-core type conjugate fiber having frictional melting-resistant performance and woven or knitted fabric using the fiber |
JP2015175066A (en) | 2014-03-13 | 2015-10-05 | 株式会社クラレ | Core sheath conjugate fiber having friction melt resistance, and woven or knitted fabric using the fiber |
WO2015159439A1 (en) | 2014-04-18 | 2015-10-22 | Kbセーレン株式会社 | Composite fiber, false twisted yarn formed from same, method for producing said false twisted yarn, and fabric |
JP2015206134A (en) | 2014-04-18 | 2015-11-19 | Kbセーレン株式会社 | composite fiber and fabric |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH03124810A (en) * | 1989-10-09 | 1991-05-28 | Ishizuka Glass Co Ltd | Fiber having antibacterial function |
JPH0913225A (en) * | 1995-06-28 | 1997-01-14 | Teijin Ltd | Sheath-core type deodorant and antimicrobial conjugate fiber |
-
2018
- 2018-03-30 JP JP2018067502A patent/JP7014662B2/en active Active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2653815B2 (en) | 1988-02-18 | 1997-09-17 | 旭化成工業株式会社 | Fiber material containing metal ions |
JP2000096350A (en) | 1998-07-16 | 2000-04-04 | Mitsubishi Rayon Co Ltd | Sheath-core type conjugate fiber having frictional melting-resistant performance and woven or knitted fabric using the fiber |
JP2015175066A (en) | 2014-03-13 | 2015-10-05 | 株式会社クラレ | Core sheath conjugate fiber having friction melt resistance, and woven or knitted fabric using the fiber |
WO2015159439A1 (en) | 2014-04-18 | 2015-10-22 | Kbセーレン株式会社 | Composite fiber, false twisted yarn formed from same, method for producing said false twisted yarn, and fabric |
JP2015206134A (en) | 2014-04-18 | 2015-11-19 | Kbセーレン株式会社 | composite fiber and fabric |
Also Published As
Publication number | Publication date |
---|---|
JP2019178443A (en) | 2019-10-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US5047448A (en) | Antimicrobial-shaped article and a process for producing the same | |
JP2013511628A (en) | Fibers and articles having a combination of fire resistance and enhanced reversible thermal properties | |
CN101184873A (en) | Multi-component fibers having enhanced reversible thermal properties and methods of manufacturing thereof | |
JP2008303525A (en) | X-ray detectable monofilament | |
JP2004011032A (en) | Temperature control fiber, and temperature control fabric member | |
WO2009101661A1 (en) | Monofilament allowing contrast x-ray radiography | |
JP7014662B2 (en) | Friction-proof composite fibers, fabrics and clothing | |
JP5217056B2 (en) | Method for producing water-absorbent woven or knitted fabric | |
JP2012112055A (en) | Core-sheath type polyester conjugate fiber | |
KR20190067763A (en) | The polymeric fiber and the fiber structure made thereof | |
JP5133546B2 (en) | Hygroscopic polyester fiber | |
WO2002077100A2 (en) | Compositions for enhanced thermal bonding | |
JP2011157646A (en) | Polyester microfiber | |
JP2003268628A (en) | Antibacterial polyester fiber | |
JP4797905B2 (en) | Knitted fabric containing nanofiber fibers | |
JP4581428B2 (en) | Light-weight blended fiber with excellent light-shielding properties, and fiber products made of the same | |
JP2012001827A (en) | Polyester fiber | |
JP2009174069A (en) | Method for producing water-absorbing polylactic acid fiber structure, water-absorbing polylactic acid fiber structure and fiber product | |
JP2593890B2 (en) | Antibacterial molded article and method for producing the same | |
JP2003064558A (en) | Comfortable knitted fabric | |
JP4704197B2 (en) | Polyester fiber | |
JP2004183196A (en) | Polyester conjugate fiber excellent in lightweight property | |
JP2005041997A (en) | Biodegradable resin composition and sheet material using the same | |
JP2000160450A (en) | Woven/knitted fabric with high moisture absorbability/ releasability and thermal insulation | |
WO2005005699A1 (en) | Fabric having temperature control function |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20181122 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20200630 |
|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20200630 |
|
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20210513 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20210608 |
|
A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20210806 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20211007 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20211221 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20220120 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 7014662 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |