JP6587947B2 - Blood / virus barrier laminate fabric and method for producing the same - Google Patents
Blood / virus barrier laminate fabric and method for producing the same Download PDFInfo
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- JP6587947B2 JP6587947B2 JP2016013445A JP2016013445A JP6587947B2 JP 6587947 B2 JP6587947 B2 JP 6587947B2 JP 2016013445 A JP2016013445 A JP 2016013445A JP 2016013445 A JP2016013445 A JP 2016013445A JP 6587947 B2 JP6587947 B2 JP 6587947B2
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- blood
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- mass
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- 239000004744 fabric Substances 0.000 title claims description 146
- 230000004888 barrier function Effects 0.000 title claims description 54
- 241000700605 Viruses Species 0.000 title claims description 50
- 239000008280 blood Substances 0.000 title claims description 41
- 210000004369 blood Anatomy 0.000 title claims description 41
- 238000004519 manufacturing process Methods 0.000 title claims description 14
- 239000012790 adhesive layer Substances 0.000 claims description 57
- 230000001681 protective effect Effects 0.000 claims description 49
- 239000012528 membrane Substances 0.000 claims description 46
- 239000004417 polycarbonate Substances 0.000 claims description 44
- 229920000515 polycarbonate Polymers 0.000 claims description 44
- 229920005749 polyurethane resin Polymers 0.000 claims description 41
- 238000005406 washing Methods 0.000 claims description 35
- 239000010419 fine particle Substances 0.000 claims description 34
- 238000004659 sterilization and disinfection Methods 0.000 claims description 34
- 230000001954 sterilising effect Effects 0.000 claims description 33
- 238000011282 treatment Methods 0.000 claims description 31
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 27
- 238000005299 abrasion Methods 0.000 claims description 19
- 239000000853 adhesive Substances 0.000 claims description 19
- 230000001070 adhesive effect Effects 0.000 claims description 19
- 238000000034 method Methods 0.000 claims description 18
- 229920002994 synthetic fiber Polymers 0.000 claims description 8
- 239000012209 synthetic fiber Substances 0.000 claims description 8
- 229920000728 polyester Polymers 0.000 claims description 7
- 239000002473 artificial blood Substances 0.000 claims description 5
- 238000011156 evaluation Methods 0.000 claims description 5
- 239000010408 film Substances 0.000 description 86
- 230000000052 comparative effect Effects 0.000 description 28
- 239000011342 resin composition Substances 0.000 description 27
- 239000000203 mixture Substances 0.000 description 21
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 18
- 229920005989 resin Polymers 0.000 description 18
- 239000011347 resin Substances 0.000 description 18
- -1 polytetrafluoroethylene Polymers 0.000 description 17
- 238000000576 coating method Methods 0.000 description 13
- 239000011248 coating agent Substances 0.000 description 12
- 238000009472 formulation Methods 0.000 description 12
- 239000007787 solid Substances 0.000 description 12
- 239000000463 material Substances 0.000 description 11
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 239000003795 chemical substances by application Substances 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 238000001723 curing Methods 0.000 description 7
- 150000002009 diols Chemical class 0.000 description 7
- 239000000178 monomer Substances 0.000 description 7
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 7
- 239000004810 polytetrafluoroethylene Substances 0.000 description 7
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 238000004078 waterproofing Methods 0.000 description 5
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 239000005056 polyisocyanate Substances 0.000 description 4
- 229920001228 polyisocyanate Polymers 0.000 description 4
- OAHBDANOQZTKQO-LYKKTTPLSA-N (2s)-2,6-diamino-7-oxooctadecanoic acid Chemical compound CCCCCCCCCCCC(=O)C(N)CCC[C@H](N)C(O)=O OAHBDANOQZTKQO-LYKKTTPLSA-N 0.000 description 3
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 3
- 229920000178 Acrylic resin Polymers 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 3
- 239000004970 Chain extender Substances 0.000 description 3
- 229920006358 Fluon Polymers 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 239000012948 isocyanate Substances 0.000 description 3
- 150000002513 isocyanates Chemical class 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 230000035699 permeability Effects 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000005871 repellent Substances 0.000 description 3
- 230000002940 repellent Effects 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- HGQSXVKHVMGQRG-UHFFFAOYSA-N dioctyltin Chemical compound CCCCCCCC[Sn]CCCCCCCC HGQSXVKHVMGQRG-UHFFFAOYSA-N 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 2
- 239000012943 hotmelt Substances 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 230000010354 integration Effects 0.000 description 2
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 238000009991 scouring Methods 0.000 description 2
- 238000010558 suspension polymerization method Methods 0.000 description 2
- FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 description 1
- VKSWWACDZPRJAP-UHFFFAOYSA-N 1,3-dioxepan-2-one Chemical compound O=C1OCCCCO1 VKSWWACDZPRJAP-UHFFFAOYSA-N 0.000 description 1
- OVBFMUAFNIIQAL-UHFFFAOYSA-N 1,4-diisocyanatobutane Chemical compound O=C=NCCCCN=C=O OVBFMUAFNIIQAL-UHFFFAOYSA-N 0.000 description 1
- CDMDQYCEEKCBGR-UHFFFAOYSA-N 1,4-diisocyanatocyclohexane Chemical compound O=C=NC1CCC(N=C=O)CC1 CDMDQYCEEKCBGR-UHFFFAOYSA-N 0.000 description 1
- BJELTSYBAHKXRW-UHFFFAOYSA-N 2,4,6-triallyloxy-1,3,5-triazine Chemical compound C=CCOC1=NC(OCC=C)=NC(OCC=C)=N1 BJELTSYBAHKXRW-UHFFFAOYSA-N 0.000 description 1
- OLQFXOWPTQTLDP-UHFFFAOYSA-N 2-(2-hydroxyethoxy)ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCO OLQFXOWPTQTLDP-UHFFFAOYSA-N 0.000 description 1
- RWXMAAYKJDQVTF-UHFFFAOYSA-N 2-(2-hydroxyethoxy)ethyl prop-2-enoate Chemical compound OCCOCCOC(=O)C=C RWXMAAYKJDQVTF-UHFFFAOYSA-N 0.000 description 1
- ZKLMKZINKNMVKA-UHFFFAOYSA-N 2-(2-hydroxypropoxy)propan-1-ol;2-methylprop-2-enoic acid Chemical compound CC(=C)C(O)=O.CC(O)COC(C)CO ZKLMKZINKNMVKA-UHFFFAOYSA-N 0.000 description 1
- YATYDCQGPUOZGZ-UHFFFAOYSA-N 2-(2-hydroxypropoxy)propan-1-ol;prop-2-enoic acid Chemical compound OC(=O)C=C.CC(O)COC(C)CO YATYDCQGPUOZGZ-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 description 1
- CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- FZHZPYGRGQZBCV-UHFFFAOYSA-N 2-propylpropane-1,3-diol Chemical compound CCCC(CO)CO FZHZPYGRGQZBCV-UHFFFAOYSA-N 0.000 description 1
- 239000005997 Calcium carbide Substances 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 239000004641 Diallyl-phthalate Substances 0.000 description 1
- OIFBSDVPJOWBCH-UHFFFAOYSA-N Diethyl carbonate Chemical compound CCOC(=O)OCC OIFBSDVPJOWBCH-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- 239000004831 Hot glue Substances 0.000 description 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- 239000004472 Lysine Substances 0.000 description 1
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 1
- 239000004594 Masterbatch (MB) Substances 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 241000270666 Testudines Species 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 1
- OKKRPWIIYQTPQF-UHFFFAOYSA-N Trimethylolpropane trimethacrylate Chemical compound CC(=C)C(=O)OCC(CC)(COC(=O)C(C)=C)COC(=O)C(C)=C OKKRPWIIYQTPQF-UHFFFAOYSA-N 0.000 description 1
- JUDXBRVLWDGRBC-UHFFFAOYSA-N [2-(hydroxymethyl)-3-(2-methylprop-2-enoyloxy)-2-(2-methylprop-2-enoyloxymethyl)propyl] 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(CO)(COC(=O)C(C)=C)COC(=O)C(C)=C JUDXBRVLWDGRBC-UHFFFAOYSA-N 0.000 description 1
- HVVWZTWDBSEWIH-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(COC(=O)C=C)COC(=O)C=C HVVWZTWDBSEWIH-UHFFFAOYSA-N 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 230000032683 aging Effects 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
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- JZQAAQZDDMEFGZ-UHFFFAOYSA-N bis(ethenyl) hexanedioate Chemical compound C=COC(=O)CCCCC(=O)OC=C JZQAAQZDDMEFGZ-UHFFFAOYSA-N 0.000 description 1
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000004650 carbonic acid diesters Chemical class 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- KBLWLMPSVYBVDK-UHFFFAOYSA-N cyclohexyl prop-2-enoate Chemical compound C=CC(=O)OC1CCCCC1 KBLWLMPSVYBVDK-UHFFFAOYSA-N 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 description 1
- ROORDVPLFPIABK-UHFFFAOYSA-N diphenyl carbonate Chemical compound C=1C=CC=CC=1OC(=O)OC1=CC=CC=C1 ROORDVPLFPIABK-UHFFFAOYSA-N 0.000 description 1
- 239000000986 disperse dye Substances 0.000 description 1
- 238000012674 dispersion polymerization Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010556 emulsion polymerization method Methods 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 238000013008 moisture curing Methods 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000011164 primary particle Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 1
- QTECDUFMBMSHKR-UHFFFAOYSA-N prop-2-enyl prop-2-enoate Chemical compound C=CCOC(=O)C=C QTECDUFMBMSHKR-UHFFFAOYSA-N 0.000 description 1
- BOQSSGDQNWEFSX-UHFFFAOYSA-N propan-2-yl 2-methylprop-2-enoate Chemical compound CC(C)OC(=O)C(C)=C BOQSSGDQNWEFSX-UHFFFAOYSA-N 0.000 description 1
- LYBIZMNPXTXVMV-UHFFFAOYSA-N propan-2-yl prop-2-enoate Chemical compound CC(C)OC(=O)C=C LYBIZMNPXTXVMV-UHFFFAOYSA-N 0.000 description 1
- NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000010345 tape casting Methods 0.000 description 1
- CLZWAWBPWVRRGI-UHFFFAOYSA-N tert-butyl 2-[2-[2-[2-[bis[2-[(2-methylpropan-2-yl)oxy]-2-oxoethyl]amino]-5-bromophenoxy]ethoxy]-4-methyl-n-[2-[(2-methylpropan-2-yl)oxy]-2-oxoethyl]anilino]acetate Chemical compound CC1=CC=C(N(CC(=O)OC(C)(C)C)CC(=O)OC(C)(C)C)C(OCCOC=2C(=CC=C(Br)C=2)N(CC(=O)OC(C)(C)C)CC(=O)OC(C)(C)C)=C1 CLZWAWBPWVRRGI-UHFFFAOYSA-N 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 229940096522 trimethylolpropane triacrylate Drugs 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Landscapes
- Professional, Industrial, Or Sporting Protective Garments (AREA)
- Laminated Bodies (AREA)
Description
本発明は、手術衣、無菌衣、又は手術用ドレープなどに好適な血液・ウイルスバリア性積層布帛、及びその製造方法に関する。 The present invention relates to a blood / virus barrier laminated fabric suitable for surgical gowns, aseptic gowns, or surgical drapes, and a method for producing the same.
表地、樹脂膜及び裏地がこの順に積層された血液・ウイルスバリア性積層布帛が知られている。例えば、特許文献1には、表地用繊維布帛、乾式膜、湿式膜、接着剤層及び裏地用繊維布帛が、この順に積層された布帛が記載されている。また、特許文献2には、表地、第一接着剤層、微多孔質ポリテトラフルオロエチレンフィルム、第二接着剤層及び裏地が、この順に積層された布帛が記載されている。 A blood / virus barrier laminated fabric in which a surface material, a resin film, and a lining material are laminated in this order is known. For example, Patent Document 1 describes a fabric in which a surface fabric fiber fabric, a dry film, a wet membrane, an adhesive layer, and a backing fiber fabric are laminated in this order. Patent Document 2 describes a fabric in which a surface material, a first adhesive layer, a microporous polytetrafluoroethylene film, a second adhesive layer, and a backing are laminated in this order.
特許文献1及び2に記載の積層布帛は、何れも初期の血液・ウイルスバリア性に優れるだけでなく、工業洗濯及び湿熱滅菌処理に対する耐久性にも優れる。そのため、手術衣又は手術用ドレープなどの医療用途に好適に使用される。さらに、これらは透湿性にも優れるため、手術衣などに快適な着用感を付与できる。 The laminated fabrics described in Patent Documents 1 and 2 are not only excellent in initial blood / virus barrier properties but also excellent in durability against industrial washing and wet heat sterilization treatment. Therefore, it is suitably used for medical applications such as a surgical gown or a surgical drape. Furthermore, since these are also excellent in moisture permeability, a comfortable wearing feeling can be imparted to a surgical gown or the like.
しかしながら、特許文献1及び2に記載の積層布帛は、表裏における布帛を必要とし、かつ製造工程が複雑であることから、製造コストが嵩む場合がある。また、着用快適性を向上させるために透湿性を発揮させえているが故に、過酷な着用、洗濯及び滅菌の繰り返しにより、血液・ウイルスバリアが通過しやすくなる危険性を孕んでいる。また、表裏の布帛が厚みと重量感とを与えてしまい、耐剥離性に劣るばかりか、軽量で取り扱い易い積層布帛が望まれる昨今の要望に、十分に応えられていない。ここで、軽量性を発現させるために片面のみに布帛を用いた場合は、耐摩耗性が不十分となってしまう However, the laminated fabrics described in Patent Documents 1 and 2 require fabrics on the front and back sides, and the manufacturing process is complicated, so that the manufacturing cost may increase. Further, since the moisture permeability is exhibited in order to improve the wearing comfort, there is a risk that the blood / virus barrier may easily pass through repeated severe wearing, washing and sterilization. Further, the fabrics on the front and back sides give a thickness and a feeling of weight, and are not only inferior in peel resistance, but also have not fully met the recent demand for a lightweight and easy-to-handle laminated fabric. Here, when a fabric is used only on one side in order to develop lightness, the wear resistance is insufficient.
本発明は、上記従来技術の欠点を解消するものであり、簡易な操作で得られ、工業洗濯及び湿熱滅菌処理後においても血液・ウイルスバリア性を発揮し、さらに耐剥離性に優れ、片面のみに布帛を採用した場合であっても耐摩耗性に優れる積層布帛を提供することを課題とする。 The present invention eliminates the above-mentioned drawbacks of the prior art, is obtained by a simple operation, exhibits blood / virus barrier properties even after industrial washing and wet heat sterilization treatment, and has excellent peel resistance, only on one side. It is an object of the present invention to provide a laminated fabric having excellent wear resistance even when a fabric is employed.
本発明者らは、各々の厚み及び組成が特定のものである接着剤層、及び防水膜、並びに組成が特定のものである保護膜を、この順で基布上に積層することで、上記の課題を解決できることを初めて見出し、本発明に到達した。 The inventors have laminated the adhesive layer having a specific thickness and composition, a waterproof film, and a protective film having a specific composition on the base fabric in this order. The inventors found for the first time that the above problem can be solved, and reached the present invention.
すなわち、本発明は以下の(1)〜(6)を要旨とする。
(1)ポリエステル系合成繊維を含む基布の片面に、接着剤層、防水膜及び保護膜がこの順に積層されて含まれる血液・ウイルスバリア性積層布帛であって、前記接着剤層はポリカーボネート系ポリウレタン樹脂を主成分として含有する硬化型接着剤を含み、かつ厚みが15〜50μmであり、前記防水膜はポリカーボネート系ポリウレタン樹脂100質量部、及び架橋アクリル微粒子3〜30質量部を含有し、かつ厚みが7〜20μmであり、前記保護膜はポリカーボネート系ポリウレタン樹脂100質量部、及び耐摩耗性向上剤8〜35質量部を含有する、血液・ウイルスバリア性積層布帛。
(2)前記保護膜の厚みが1〜10μmである、(1)の血液・ウイルスバリア性積層布帛。
(3)前記基布の厚みが40〜100μmであり、前記接着剤層の厚みが前記基布の厚みに対し2/5以下である、(1)又は(2)の血液・ウイルスバリア性積層布帛。
That is, the gist of the present invention is the following (1) to (6).
(1) A blood / virus barrier laminate fabric in which an adhesive layer, a waterproof membrane and a protective membrane are laminated in this order on one side of a base fabric containing a polyester synthetic fiber, wherein the adhesive layer is a polycarbonate fabric Including a curable adhesive containing a polyurethane resin as a main component and having a thickness of 15 to 50 μm, the waterproof film containing 100 parts by mass of a polycarbonate-based polyurethane resin and 3 to 30 parts by mass of crosslinked acrylic fine particles; and A blood / virus barrier laminate fabric having a thickness of 7 to 20 μm and the protective film comprising 100 parts by mass of a polycarbonate-based polyurethane resin and 8 to 35 parts by mass of an abrasion resistance improver.
(2) The blood / virus barrier laminate fabric according to (1), wherein the protective film has a thickness of 1 to 10 μm.
(3) The blood / virus barrier laminate according to (1) or (2), wherein the thickness of the base fabric is 40 to 100 μm and the thickness of the adhesive layer is 2/5 or less with respect to the thickness of the base fabric. Fabric.
(4)工業洗濯10回分と湿熱滅菌処理10回分との連続処理を1サイクルとして、10サイクル処理後に、ASTM F 1670−08B法に従って評価した人工血液バリア性の判定が合格である、(1)〜(3)の何れかの血液・ウイルスバリア性積層布帛。
(5)工業洗濯10回分と湿熱滅菌処理10回分との連続処理を1サイクルとして、10サイクル処理後に、ASTM F 1671−07B法に従って評価したウイルスバリア性の判定が合格である、(1)〜(4)の何れかの血液・ウイルスバリア性積層布帛。
(4) The determination of the artificial blood barrier property evaluated according to the ASTM F 1670-08B method after the 10-cycle treatment, with a continuous treatment of 10 industrial washings and 10 wet heat sterilization treatments as one cycle, (1) The blood / virus barrier laminated fabric according to any one of to (3).
(5) The determination of the virus barrier property evaluated according to the ASTM F 1671-07B method after passing 10 cycles after the continuous treatment of 10 times of industrial washing and 10 times of wet heat sterilization treatment is passed, (1) to The blood / virus barrier laminate fabric according to any one of (4).
(6)(1)〜(5)の何れか1項に記載の血液・ウイルスバリア性積層布帛を製造する方法であって、前記基布と前記防水膜とを、前記接着剤層で貼りあわせた後、前記防水膜上に前記保護膜を形成する、血液・ウイルスバリア性積層布帛の製造方法。 (6) A method for producing a blood / virus barrier laminate fabric according to any one of (1) to (5), wherein the base fabric and the waterproof membrane are bonded together with the adhesive layer. Then, the method for producing a blood / virus barrier laminate fabric, wherein the protective film is formed on the waterproof film.
本発明の積層布帛は、ポリカーボネート系ポリウレタン樹脂を主成分とする接着剤層、防水膜及び保護膜をこの順で基布上に積層するとともに、接着剤層に含まれる接着剤を硬化型とし、防水膜においてポリカーボネート系ポリウレタン樹脂との相溶性に優れ耐熱性向上にも寄与し得る架橋アクリル微粒子を特定の割合で含有させているために、本発明の積層布帛は、防水性、血液・ウイルスバリア性、工業洗濯及び湿熱滅菌処理の耐久性、並びに風合いに優れるとともに、基布と防水膜との接着性向上及び一体化が図られ耐剥離性に顕著に優れる。さらに本発明の積層布帛は、保護膜に耐摩耗性向上剤を特定の割合で含有させているために、表面の外観品位、タッチ感、及び耐摩耗性にも優れる。本発明の積層布帛は医療用衣服・資材一般に好適であり、特に手術衣、無菌衣、又は手術用ドレープなどの過酷な条件下での工業洗濯及び湿熱滅菌処理が施されるリユース素材において、好ましく使用できる。 In the laminated fabric of the present invention, an adhesive layer mainly composed of a polycarbonate-based polyurethane resin, a waterproof membrane and a protective membrane are laminated on the base fabric in this order, and the adhesive contained in the adhesive layer is a curable type. In the waterproof membrane, the laminated fabric of the present invention has a waterproof property, blood / virus barrier because it contains a specific proportion of cross-linked acrylic fine particles that are excellent in compatibility with the polycarbonate-based polyurethane resin and can contribute to an improvement in heat resistance. Property, durability of industrial washing and wet heat sterilization treatment, and texture, as well as improved adhesion and integration between the base fabric and the waterproof membrane, and remarkably excellent peel resistance. Furthermore, the laminated fabric of the present invention is excellent in surface appearance quality, touch feeling, and abrasion resistance because the protective film contains the wear resistance improver in a specific ratio. The laminated fabric of the present invention is suitable for medical clothes and materials in general, and is particularly preferable for reuse materials that are subjected to industrial washing and wet heat sterilization treatment under severe conditions such as surgical clothes, sterile clothes, or surgical drapes. Can be used.
以下、本発明について詳細に説明する。
本発明の血液・ウイルスバリア性積層布帛(積層布帛)は、ポリエステル系合成繊維を含む基布、接着剤層、防水膜及び保護膜を有する。詳しくは、図1にて示されるように、本発明の血液・ウイルスバリア性積層布帛1は、基布2の片面に、接着剤層3、防水膜4及び保護膜5がこの順に積層されて含まれる。接着剤層、防水膜及び保護膜は、ポリカーボネート系ポリウレタン樹脂を主成分として含む。
Hereinafter, the present invention will be described in detail.
The blood / virus barrier laminate fabric (laminate fabric) of the present invention has a base fabric containing a polyester-based synthetic fiber, an adhesive layer, a waterproof membrane and a protective membrane. Specifically, as shown in FIG. 1, the blood / virus barrier laminate fabric 1 of the present invention has an adhesive layer 3, a waterproof membrane 4 and a protective membrane 5 laminated in this order on one side of a base fabric 2. included. The adhesive layer, the waterproof film and the protective film contain a polycarbonate-based polyurethane resin as a main component.
[基布]
基布としては、工業洗濯及び湿熱滅菌処理に耐え得る強度を有するものであれば、特に限定されないが、汎用性、及び高温かつ高圧下での耐湿熱性に優れるため、ポリエステル系合成繊維を主たる構成繊維とするものが好ましい。例えば、ポリエステル系合成繊維の混率が90質量%以上、好ましくは100質量%である基布が好ましい。また、軽量性及び風合いの観点から、基布の厚みは40〜100μmであることが好ましく、50〜90μmであることがより好ましい。
[Base fabric]
The base fabric is not particularly limited as long as it has a strength that can withstand industrial washing and wet heat sterilization treatment, but because of its versatility and excellent heat and humidity resistance under high temperature and high pressure, the main composition is a polyester-based synthetic fiber. What is made into a fiber is preferable. For example, a base fabric having a polyester synthetic fiber mixing ratio of 90% by mass or more, preferably 100% by mass is preferable. Further, from the viewpoint of lightness and texture, the thickness of the base fabric is preferably 40 to 100 μm, and more preferably 50 to 90 μm.
基布には、工業洗濯及び湿熱滅菌処理の耐久性を損なわない範囲で、ポリエステル系合成繊維以外の合成繊維(例えば、ナイロン6、ナイロン66のようなポリアミド系、ポリアクリルニトリル系、又はポリビニルアルコール系の合成繊維)が含まれていてもよい。基布の形態としては、織物(例えば、リップタフタ、ツイルなど)、編物、又は不織布などが挙げられる。基布には、撥水加工、カレンダー加工、制電加工又は抗菌加工などの公知の加工が施されていてもよい。 For the base fabric, synthetic fibers other than polyester-based synthetic fibers (for example, polyamides such as nylon 6 and nylon 66, polyacrylonitriles, or polyvinyl alcohol are used as long as they do not impair the durability of industrial washing and wet heat sterilization. System synthetic fibers) may be included. Examples of the form of the base fabric include woven fabric (for example, lip taffeta, twill, etc.), knitted fabric, or non-woven fabric. The base fabric may be subjected to known processing such as water repellent processing, calendar processing, antistatic processing, or antibacterial processing.
[防水膜]
防水膜は防水性に寄与するものであり、ポリカーボネート系ポリウレタン樹脂を主たる成分として含み、さらに架橋アクリル微粒子を含有する。
(ポリカーボネート系ポリウレタン樹脂)
ポリカーボネート系ポリウレタン樹脂は、それ自体が耐熱性及び耐加水分解性などに優れる。そのため、本発明の積層布帛は、工業洗濯及び湿熱滅菌処理に対する耐久性に優れる。
[Waterproof membrane]
The waterproof membrane contributes to waterproofness, contains a polycarbonate-based polyurethane resin as a main component, and further contains crosslinked acrylic fine particles.
(Polycarbonate polyurethane resin)
The polycarbonate-based polyurethane resin itself is excellent in heat resistance and hydrolysis resistance. Therefore, the laminated fabric of the present invention is excellent in durability against industrial washing and wet heat sterilization treatment.
ポリカーボネート系ポリウレタン樹脂としては、ポリカーボネートジオールと有機ポリイソシアネートとを原料とし、例えばワンショット法(ポリカーボネートジオール、有機ポリイソシアネート、及び鎖延長剤を、一括に仕込んで反応させる方法)、又はプレポリマー法(予めポリカーボネートジオールと有機ポリイソシアネートとを反応させ、次いで、鎖延長剤を加える方法)により得られる公知の樹脂が挙げられる。 As the polycarbonate-based polyurethane resin, a polycarbonate diol and an organic polyisocyanate are used as raw materials. For example, a one-shot method (a method in which a polycarbonate diol, an organic polyisocyanate, and a chain extender are charged together and reacted), or a prepolymer method ( A known resin obtained by reacting a polycarbonate diol and an organic polyisocyanate in advance and then adding a chain extender) may be mentioned.
ポリカーボネートジオールとしては、例えば、1,4−ブタンジオール、1,5−ペンタンジオール、1,6−ヘキサンジオールなどのアルキルジオール、2,2−ジメチル−1,3−プロパンジオール、2,2−ジエチル−1,3−プロパンジオール、又は2−ペンチル,2−プロピル−1,3−プロパンジオールなどの2,2−ジアルキル−1,3−プロパンジオールのような1種又は2種以上のジオールと、ジフェニルカーボネート、ジトリールカーボネートなどのジアリールカーボネート、ジメチルカーボネート、ジエチルカーボネートなどのジアルキルカーボネート、エチレンカーボネート、又はテトラメチレンカーボネートなどのアルキレンカーボネートのような1種又は2種以上の炭酸ジエステルとのエステル交換反応により得られるものが挙げられる。なかでも、有機溶剤に対する溶解性、又は溶融樹脂としての粘性などの観点から、結晶性を低減させるために、ジオールとしては2,2−ジアルキル−1,3−プロパンジオールポリカーボネートジオールを主体とするものが好ましく、高圧下での湿熱滅菌処理に対する耐久性の観点から、炭酸ジエステルとしてはジアリールカーボネートを主体とするものが好ましい。 Examples of the polycarbonate diol include alkyl diols such as 1,4-butanediol, 1,5-pentanediol, and 1,6-hexanediol, 2,2-dimethyl-1,3-propanediol, and 2,2-diethyl. -1,3-propanediol, or one or more diols such as 2,2-dialkyl-1,3-propanediol such as 2-pentyl, 2-propyl-1,3-propanediol, and By transesterification with one or more carbonic acid diesters, such as diaryl carbonates such as diphenyl carbonate and ditolyl carbonate, dialkyl carbonates such as dimethyl carbonate and diethyl carbonate, ethylene carbonate, and alkylene carbonates such as tetramethylene carbonate. It is those, and the like. Among these, in order to reduce crystallinity from the viewpoint of solubility in an organic solvent or viscosity as a molten resin, the diol mainly comprises 2,2-dialkyl-1,3-propanediol polycarbonate diol. From the viewpoint of durability against wet heat sterilization under high pressure, the diester carbonate is mainly composed of diaryl carbonate.
有機ポリイソシアネートとしては、例えば、テトラメチレンジイソシアネート、ヘキサメチレンジイソシアネートなどの脂肪族ジイソシアネート、1,4−シクロヘキサンジイソシアネート、イソフォロンジイソシアネートなどの脂環族ジイソシアネート、キシリレンジイソシアネート、4,4’−ジフェニールジイソシアネートなどの芳香族ジイソシアネートが挙げられる。なかでも、高圧下での湿熱滅菌処理に対する耐久性の観点から、芳香族ジイソシアネートを主体とするものが好ましい。 Examples of the organic polyisocyanate include aliphatic diisocyanates such as tetramethylene diisocyanate and hexamethylene diisocyanate, alicyclic diisocyanates such as 1,4-cyclohexane diisocyanate and isophorone diisocyanate, xylylene diisocyanate, and 4,4′-diphenyl diisocyanate. And aromatic diisocyanates. Among these, those mainly composed of aromatic diisocyanate are preferable from the viewpoint of durability against wet heat sterilization under high pressure.
鎖延長剤としては、1,4−ブタンジオール、1,6−ヘキサンジオール、エチレンジアミンなどが挙げられる。これらは単独で又は2種以上を併用して用いることができる。 Examples of the chain extender include 1,4-butanediol, 1,6-hexanediol, and ethylenediamine. These can be used alone or in combination of two or more.
ポリカーボネート系ポリウレタン樹脂は、血液バリア性及びウイルスバリア性、並びに複数回の工業洗濯及び湿熱滅菌処理を施した場合のリユース性に優れるために、透湿性を有しないものであることが好ましい。 Since the polycarbonate-based polyurethane resin is excellent in blood barrier property and virus barrier property, and reusability when subjected to industrial washing and wet heat sterilization multiple times, it is preferable that the polycarbonate-based polyurethane resin does not have moisture permeability.
防水膜に含まれる樹脂(架橋アクリル微粒子以外の樹脂)としては、ポリカーボネート系ポリウレタン樹脂のみであってもよい。または、架橋アクリル微粒子との相溶性、耐熱性及び耐加水分解性(耐湿熱性)などに影響を与えない範囲で、ポリカーボネート系ポリウレタン樹脂に加えてその他の樹脂を含有させてもよい。その他の樹脂としては任意の樹脂が挙げられ、例えば、ポリエーテル系ポリウレタン樹脂、ポリエステル系ポリウレタン樹脂、ポリアクリル系樹脂などが挙げられる。耐湿熱性の観点から、防水膜を構成する全樹脂中、ポリカーボネート系ポリウレタン樹脂の割合が70質量%以上であることが好ましい。 The resin (resin other than the crosslinked acrylic fine particles) contained in the waterproof film may be only a polycarbonate-based polyurethane resin. Alternatively, other resins may be included in addition to the polycarbonate-based polyurethane resin as long as the compatibility with the crosslinked acrylic fine particles, heat resistance, hydrolysis resistance (moisture heat resistance), and the like are not affected. Examples of other resins include arbitrary resins such as polyether polyurethane resins, polyester polyurethane resins, and polyacrylic resins. From the viewpoint of moisture and heat resistance, the proportion of the polycarbonate-based polyurethane resin is preferably 70% by mass or more in the total resin constituting the waterproof film.
防水膜の厚みは7〜20μmであり、9〜18μmであることが好ましい。防水膜の厚みが7μm以上であると、基布の厚み又は組織等を問わずに防水性、及び血液・ウイルスバリア性の耐久性に優れる。防水膜の厚みが20μm以下であると、血液・ウイルスバリア性の耐久性及び風合いに優れる。 The waterproof membrane has a thickness of 7 to 20 μm, preferably 9 to 18 μm. When the thickness of the waterproof membrane is 7 μm or more, the waterproof property and the durability of blood / virus barrier properties are excellent regardless of the thickness of the base fabric or the tissue. When the thickness of the waterproof membrane is 20 μm or less, the durability and texture of blood / virus barrier properties are excellent.
(架橋アクリル微粒子)
架橋アクリル微粒子は、ポリカーボネート系ポリウレタン樹脂との相溶性に優れるため、防水膜全体の耐久性を向上させる。架橋アクリル微粒子としては、例えば、アクリル酸エステル類、又はメタクリル酸エステル類などを主成分とする重合性モノマーと、架橋性モノマーとを重合反応することにより得られる微粒子が挙げられる。
(Crosslinked acrylic fine particles)
Since the cross-linked acrylic fine particles are excellent in compatibility with the polycarbonate-based polyurethane resin, the durability of the entire waterproof membrane is improved. Examples of the crosslinked acrylic fine particles include fine particles obtained by polymerizing a polymerizable monomer mainly composed of acrylic acid esters or methacrylic acid esters and a crosslinkable monomer.
アクリル酸エステル類としては、アクリル酸メチル、アクリル酸エチル、アクリル酸プロピル、アクリル酸イソプロピル、アクリル酸ブチル、アクリル酸イソブチル、アクリル酸シクロヘキシル、アクリル酸2−エチルヘキシルなどが挙げられる。また、メタクリル酸エステル類としては、メタクリル酸メチル、メタクリル酸エチル、メタクリル酸プロピル、メタクリル酸イソプロピル、メタクリル酸ブチル、メタクリル酸イソブチルなどが挙げられる。これらを単独で又は混合して用いることができる。 Examples of the acrylate esters include methyl acrylate, ethyl acrylate, propyl acrylate, isopropyl acrylate, butyl acrylate, isobutyl acrylate, cyclohexyl acrylate, 2-ethylhexyl acrylate, and the like. Examples of methacrylic acid esters include methyl methacrylate, ethyl methacrylate, propyl methacrylate, isopropyl methacrylate, butyl methacrylate, and isobutyl methacrylate. These can be used alone or in combination.
架橋性モノマーとしては、例えば、エチレングリコールアクリレート、ジエチレングリコールアクリレート、ジプロピレングリコールアクリレート、トリメチロールプロパントリアクリレート、テトラメチロールメタントリアクリレート、エチレングリコールメタクリレート、ジエチレングリコールメタクリレート、ジプロピレングリコールメタクリレート、トリメチロールプロパントリメタクリレート、テトラメチロールメタントリメタクリレート、ジビニルベンゼン、ジビニルアジペートなどのビニル系架橋性モノマー、ジアリルフタレート、アリルアクリレート、アリルメタクリレート、トリアリルシアヌレートなどのアリル基含有架橋性モノマーなどが挙げられる。 Examples of the crosslinking monomer include ethylene glycol acrylate, diethylene glycol acrylate, dipropylene glycol acrylate, trimethylol propane triacrylate, tetramethylol methane triacrylate, ethylene glycol methacrylate, diethylene glycol methacrylate, dipropylene glycol methacrylate, trimethylol propane trimethacrylate, Examples thereof include vinyl-based crosslinkable monomers such as tetramethylolmethane trimethacrylate, divinylbenzene and divinyladipate, and allyl group-containing crosslinkable monomers such as diallyl phthalate, allyl acrylate, allyl methacrylate and triallyl cyanurate.
架橋アクリル微粒子の製造方法の一例は、以下の通りである。上記重合性モノマー及び架橋性モノマーを混合し、無機又は有機過酸化物などの重合開始剤の存在下で、一般的な懸濁重合法、ミクロ懸濁重合法、乳化重合法、又は分散重合法などを採用して製造することができる。 An example of a method for producing the crosslinked acrylic fine particles is as follows. The above-mentioned polymerizable monomer and crosslinkable monomer are mixed, and in the presence of a polymerization initiator such as inorganic or organic peroxide, a general suspension polymerization method, micro suspension polymerization method, emulsion polymerization method, or dispersion polymerization method is used. Etc. can be used for manufacturing.
架橋アクリル微粒子の形状は、特に限定されるものでないが、血液・ウイルスバリア性又は防水性(耐水圧)の観点から、球状が好ましい。また、架橋アクリル微粒子の粒子径は0.1〜20μmが好ましく、1〜15μmがより好ましい。0.1μm以上であると取扱性に優れ、防水膜中に均一に分散させ易くなり架橋アクリル微粒子の含有効果がより効果的に発現する。0.1〜20μm以下であると、防水膜中での分散性がより良好となり防水性の低下をいっそう抑制できる。 The shape of the crosslinked acrylic fine particles is not particularly limited, but is preferably spherical from the viewpoint of blood / virus barrier properties or waterproofness (water pressure resistance). The particle diameter of the crosslinked acrylic fine particles is preferably 0.1 to 20 μm, and more preferably 1 to 15 μm. When the thickness is 0.1 μm or more, the handleability is excellent, and it becomes easy to uniformly disperse in the waterproof film, and the effect of containing the crosslinked acrylic fine particles is more effectively expressed. When the thickness is 0.1 to 20 μm or less, the dispersibility in the waterproof film becomes better, and deterioration of the waterproof property can be further suppressed.
防水膜における架橋アクリル微粒子の含有量は、ポリカーボネート系ポリウレタン樹脂100質量部に対して3〜30質量部であり、6〜25質量部が好ましい。3質量部以上であると耐熱性及び耐湿熱性に優れ、さらにタック感(粘着性)が強い樹脂系においても粘着性を適切に抑制することができ、取扱性及び巻取性が良好となる。30質量部以下であると、接着剤層を介した基布との接着性に優れるため一体化が容易となり、工業洗濯及び湿熱滅菌処理の多サイクルの処理が施された場合であっても耐剥離性に優れ、さらに風合いも良好となる。さらに、30質量部を超えると防水膜中に凝集物が生じ易くなり、複数回(多サイクル)の工業洗濯及び湿熱滅菌処理が施された場合に、加圧下で膜破損の起点が発生しやすくなるため、血液・ウイルスバリア性に劣る場合がある。 The content of the crosslinked acrylic fine particles in the waterproof film is 3 to 30 parts by mass, preferably 6 to 25 parts by mass, with respect to 100 parts by mass of the polycarbonate polyurethane resin. When it is 3 parts by mass or more, the adhesiveness can be appropriately suppressed even in a resin system having excellent heat resistance and moist heat resistance, and having a strong tack feeling (adhesiveness), and handling properties and winding properties are improved. When it is 30 parts by mass or less, it is excellent in adhesion to the base fabric through the adhesive layer, so that integration becomes easy, and even when subjected to multi-cycle treatment of industrial washing and wet heat sterilization treatment, Excellent peelability and good texture. Furthermore, if it exceeds 30 parts by mass, agglomerates are likely to occur in the waterproofing membrane, and when a plurality of (multi-cycle) industrial washings and wet heat sterilization treatments are performed, the starting point of membrane damage is likely to occur under pressure. Therefore, the blood / virus barrier property may be inferior.
[接着剤層]
接着剤層は、基布と防水膜とを接着して積層する。接着剤層に含まれる接着剤は、耐久性の点からポリカーボネート系ポリウレタン樹脂を主成分とする。接着剤としては、ホットメルト型接着剤、又は溶剤型接着剤等の何れであってもよいが、接着性、工業洗濯及び湿熱滅菌処理後の耐久性、並びに耐剥離性に優れるために硬化型接着剤であることが必須である。ホットメルト型接着剤の好ましい態様としては、空気中の湿気で硬化する(湿気硬化型)接着剤、又は硬化剤とポリカーボネート系ポリウレタン樹脂とからなる2液型接着剤が挙げられる。
[Adhesive layer]
The adhesive layer is laminated by bonding the base fabric and the waterproof film. The adhesive contained in the adhesive layer is mainly composed of a polycarbonate-based polyurethane resin from the viewpoint of durability. The adhesive may be any of a hot-melt type adhesive or a solvent-type adhesive, but is curable because it has excellent adhesion, durability after industrial washing and wet heat sterilization, and peeling resistance. It is essential to be an adhesive. Preferable embodiments of the hot-melt adhesive include an adhesive that cures with moisture in the air (moisture curing type), or a two-component adhesive composed of a curing agent and a polycarbonate polyurethane resin.
接着剤層は基布と防水膜との間の接着性を損なわないように形成されるものであればよく、部分的に形成されていてもよいし、全面に形成されていてもよいが、血液・ウイルスバリア性の観点からは全面、又はほぼ全面に形成されていることが好ましく、例えば、基布に対する面積比で40〜100%の範囲で形成されていることが好ましい。接着剤層が部分的に形成されている場合、その形状としては、点状、格子状、市松模様、又は亀甲型等が挙げられる。 The adhesive layer only needs to be formed so as not to impair the adhesion between the base fabric and the waterproof membrane, may be formed partially, or may be formed on the entire surface, From the viewpoint of blood / virus barrier properties, it is preferably formed on the entire surface or almost the entire surface. For example, it is preferably formed in an area ratio of 40 to 100% with respect to the base fabric. When the adhesive layer is partially formed, examples of the shape thereof include a dot shape, a lattice shape, a checkered pattern, or a turtle shell shape.
接着剤層の厚みは15〜50μmであり、18〜40μmであることが好ましい。15μm以上であると接着力が十分となるため耐剥離性に優れる。50μm以下であると工業洗濯及び湿熱滅菌処理の耐久性に優れ、さらに風合いが良好となり可撓性に優れる積層布帛を得ることができる。 The thickness of the adhesive layer is 15 to 50 μm, and preferably 18 to 40 μm. When the thickness is 15 μm or more, the adhesive strength is sufficient, and the peel resistance is excellent. When the thickness is 50 μm or less, a laminated fabric having excellent durability for industrial washing and wet heat sterilization, and a good texture and excellent flexibility can be obtained.
基布が薄地(例えば、40〜100μm程度)である場合、又は、例えば、経糸若しくは緯糸として繊度が22〜56dtexであるポリエチレンテレフタレートマルチフィラメントを用いたタフタ、又はリップタフタなどである場合には、接着剤層の厚みは、基布の厚みに対し2/5以下とすることが好ましく、1/3以下とすることがより好ましい。接着剤層の厚みをこうした範囲とすることで、軽量性により優れるとともに引裂強力も良好なものとなり、さらに接着剤層を過度に厚くしないことで耐揉性にも優れる積層布帛が得られる。加えて、基布と接着剤層との間での負荷を受け難く、その結果、多サイクルの工業洗濯及び湿熱滅菌処理を施した場合であっても、接着剤層の部分的な剥離が抑制され、血液・ウイルスバリア性に優れるものとなる。なお、本発明でいう基布の厚みとは、接着剤層、防水膜、保護膜のような樹脂膜が形成されていない基布における平均的な厚みを言う。 When the base fabric is thin (for example, about 40 to 100 μm), or when it is a taffeta using a polyethylene terephthalate multifilament having a fineness of 22 to 56 dtex as a warp or weft, or a lip taffeta, The thickness of the adhesive layer is preferably 2/5 or less, more preferably 1/3 or less with respect to the thickness of the base fabric. By setting the thickness of the adhesive layer in such a range, a lightweight fabric and excellent tear strength are obtained, and a laminated fabric having excellent weather resistance can be obtained by making the adhesive layer not excessively thick. In addition, it is difficult to receive a load between the base fabric and the adhesive layer, and as a result, partial peeling of the adhesive layer is suppressed even when subjected to multi-cycle industrial washing and wet heat sterilization treatment. And has excellent blood / virus barrier properties. In addition, the thickness of the base fabric as used in the field of this invention means the average thickness in the base fabric in which the resin film like an adhesive bond layer, a waterproof film, and a protective film is not formed.
[保護膜]
本発明の積層布帛においては、防水膜上に、防水性、耐剥離性、耐摩耗性、耐久性向上に寄与する保護膜が形成されている。保護膜は、耐熱性及び耐湿熱性に優れるポリカーボネート系ポリウレタン樹脂を主成分として含有し、さらに耐摩耗性向上剤を含有する。耐摩耗性向上剤は、保護膜表面において、滑り感、タッチ感及びマット感を向上させるとともに、耐摩耗性を向上させる。耐摩耗性向上剤の具体例としては、シリカ、アルミナ、酸化チタン、炭化カルシウム、架橋アクリル樹脂、架橋ポリスチレン樹脂、シリコーン樹脂、若しくはポリテトラフルオロエチレン等からなる微粒子、又はNε−ラウロイル−L−リジン等のような平板状の粉体物が挙げられる。なかでも、架橋アクリル樹脂若しくはポリテトラフルオロエチレンからなる微粒子、又はNε−ラウロイル−L−リジンが好ましく、架橋アクリル樹脂若しくはポリテトラフルオロエチレンからなる微粒子が特に好ましい。
[Protective film]
In the laminated fabric of the present invention, a protective film that contributes to improvement of waterproofness, peel resistance, wear resistance, and durability is formed on the waterproof film. The protective film contains, as a main component, a polycarbonate-based polyurethane resin that is excellent in heat resistance and moist heat resistance, and further contains an abrasion resistance improver. The wear resistance improver improves the wear resistance as well as improving the slipping feeling, touch feeling and mat feeling on the surface of the protective film. Specific examples of the wear resistance improver include fine particles of silica, alumina, titanium oxide, calcium carbide, crosslinked acrylic resin, crosslinked polystyrene resin, silicone resin, polytetrafluoroethylene, or the like, or N ε -lauroyl-L—. A flat powder such as lysine can be used. Among these, fine particles made of a cross-linked acrylic resin or polytetrafluoroethylene, or N ε -lauroyl-L-lysine is preferable, and fine particles made of a cross-linked acrylic resin or polytetrafluoroethylene are particularly preferable.
耐摩耗性向上剤の含有量は、保護膜に含まれるポリカーボネート系ポリウレタン樹脂100質量部に対して8〜35質量部であり、10〜30質量部が好ましい。8〜35質量部であると多サイクルの工業洗濯及び湿熱滅菌処理を施した場合であっても、耐摩耗性等に優れる。詳しくは、耐摩耗性向上剤の含有量が8質量部以上であると、工業洗濯及び湿熱滅菌処理の多サイクル処理後での耐久性、及び耐摩耗性に優れる。一方、35質量部以下であると、風合いが硬化せず、保護膜を形成するための組成物(保護膜形成用樹脂組成物)を塗布する際に塗布筋等の発生を抑制することができ、外観品位にも優れる。 The content of the wear resistance improver is 8 to 35 parts by weight, preferably 10 to 30 parts by weight, based on 100 parts by weight of the polycarbonate-based polyurethane resin contained in the protective film. Even if it is a case where multi-cycle industrial washing and wet heat sterilization processing are performed as it is 8-35 mass parts, it is excellent in abrasion resistance etc. Specifically, when the content of the wear resistance improver is 8 parts by mass or more, the durability and the wear resistance after multi-cycle treatment of industrial washing and wet heat sterilization treatment are excellent. On the other hand, when the amount is 35 parts by mass or less, the texture is not cured, and the application of a composition for forming a protective film (resin composition for forming a protective film) can suppress the occurrence of application stripes and the like. Excellent appearance quality.
保護膜の厚みは1〜10μmであることが好ましく、3〜7μmであることがより好ましい。保護膜の厚みが1μm以上であると、防水性、耐剥離性、耐摩耗性、耐熱性、耐湿熱性を発現させることができる。保護膜の厚みが10μm以下であると、特に基布が薄手生地であっても風合い硬化を抑制することができ、物性の向上が飽和することがないという利点がある。 The thickness of the protective film is preferably 1 to 10 μm, and more preferably 3 to 7 μm. When the thickness of the protective film is 1 μm or more, waterproofness, peel resistance, abrasion resistance, heat resistance, and heat and humidity resistance can be exhibited. When the thickness of the protective film is 10 μm or less, there is an advantage that texture hardening can be suppressed even when the base fabric is a thin fabric, and the improvement in physical properties is not saturated.
[積層布帛の製造方法]
上記のような本発明の血液・ウイルスバリア性積層布帛の製造方法の一例について、以下に説明する。詳しくは、本発明の製造方法としては、まず基布と防水膜とを準備する。そして、基布と防水膜とを接着剤層を介して貼り合わせた後、防水膜上に保護膜を形成する。
[Method for producing laminated fabric]
An example of the method for producing the blood / virus barrier laminate fabric of the present invention as described above will be described below. Specifically, as a manufacturing method of the present invention, first, a base fabric and a waterproof film are prepared. And after bonding together a base fabric and a waterproof film through an adhesive bond layer, a protective film is formed on a waterproof film.
防水膜の調製方法について以下に述べる。防水膜は防水膜形成用樹脂組成物(ポリカーボネート系ポリウレタン樹脂、架橋アクリル微粒子、及び有機溶剤などを含む組成物)を用いて調製される。防水膜形成用樹脂組成物においてホットメルトタイプの樹脂を使用する場合は、樹脂中に架橋アクリル微粒子を高濃度で混練させてマスターバッチを作成し、所望の組成となるように架橋アクリル微粒子、必要に応じてさらなる樹脂を混合することで防水膜形成用樹脂組成物を調製する。そして、Tダイなどを用いて厚みを調整しながら、この樹脂組成物を離型材(離型紙、離型布又は離型フィルム等)の表面にフィルム状に押出成形し防水膜を形成することができる。また、防水膜形成用樹脂組成物において溶液タイプの樹脂を使用する場合は、樹脂及び溶媒を混合させた混合物中に架橋アクリル微粒子を分散させ、粘度を所望する範囲に調整し防水膜形成用樹脂組成物を得た後、離型材上に、所望とする厚みになるように、例えばコンマコータなどを用いて塗布し、例えば80〜150℃で1〜5分間、乾燥することで、防水膜を形成することができる(乾式コーティング法)。離型材は、後述のように基布と防水膜とを貼合わせた後又は熟成した後に、適宜に取り除くことができる。 A method for preparing the waterproof membrane is described below. The waterproof film is prepared using a waterproof film-forming resin composition (a composition containing a polycarbonate-based polyurethane resin, crosslinked acrylic fine particles, an organic solvent, and the like). When using a hot melt type resin in a resin composition for forming a waterproof film, a cross-linked acrylic fine particle is necessary so that a master batch is prepared by kneading cross-linked acrylic fine particles in the resin at a high concentration. According to the above, a resin composition for forming a waterproof film is prepared by mixing additional resin. Then, while adjusting the thickness using a T-die or the like, the resin composition is extruded into a film shape on the surface of a release material (release paper, release cloth, release film, etc.) to form a waterproof film. it can. Also, when using a solution-type resin in the resin composition for waterproofing film formation, the crosslinked acrylic fine particles are dispersed in a mixture in which the resin and the solvent are mixed, and the viscosity is adjusted to a desired range, so that the waterproof film forming resin is used. After obtaining the composition, it is applied on the release material so as to have a desired thickness, for example, using a comma coater, and dried at 80 to 150 ° C. for 1 to 5 minutes to form a waterproof film. (Dry coating method). The mold release material can be appropriately removed after the base fabric and the waterproof film are bonded or aged as described later.
次に、基布、若しくは防水膜の何れかの片面、又は離型材が付与された防水膜における防水膜側の表面に、接着剤層を形成する。例えば、コンマロール、グラビアロール、ロータリースクリーンなどを用い、ホットメルトタイプの接着剤を用いる場合であれば、接着剤層形成用樹脂組成物(接着剤、硬化剤、有機溶剤及び触媒などを含む組成物)を基布又は防水膜の片面に塗布した後に冷却し、接着剤層を形成する。溶液タイプの接着剤を用いる場合であれば、接着剤層形成用樹脂組成物を基布又は防水膜の片面に塗布した後に、80〜150℃で1〜5分間乾燥させて接着剤層を形成する。又は、離型材付き防水膜の防水膜の上に、同様の方法で接着剤層を形成する。その後、接着剤層を介して基布と防水膜とを貼り合わせ、これらを圧着或いは熱圧着した後、常温〜40℃の温度で3〜7日間熟成させることができる。なお、接着剤層を基布表面ではなく防水膜表面に直接形成し、基布と防水膜とを貼り合わせる手法を採用すると、接着剤層形成用樹脂組成物を低粘度とした場合であっても、塗布時に基布を構成する繊維同士の空隙から漏れることがなく、また基布表面の凹凸によらず塗布が容易であるという利点がある。 Next, an adhesive layer is formed on one surface of the base fabric or the waterproof membrane, or on the waterproof membrane-side surface of the waterproof membrane provided with a release material. For example, when using a hot roll type adhesive using a comma roll, gravure roll, rotary screen or the like, a resin composition for forming an adhesive layer (a composition containing an adhesive, a curing agent, an organic solvent, a catalyst, etc.) The product is applied to one side of the base fabric or waterproof membrane, and then cooled to form an adhesive layer. If a solution type adhesive is used, after applying the adhesive layer forming resin composition to one side of the base fabric or waterproof membrane, the adhesive layer is formed by drying at 80 to 150 ° C. for 1 to 5 minutes. To do. Alternatively, an adhesive layer is formed by the same method on the waterproof film of the waterproof film with a release material. Then, after bonding a base fabric and a waterproofing membrane through an adhesive bond layer, these are crimped | bonded or thermocompression bonded, it can be aged for 3 to 7 days at the temperature of normal temperature-40 degreeC. In addition, when the adhesive layer is formed directly on the surface of the waterproof membrane, not the surface of the base fabric, and the technique of bonding the base fabric and the waterproof membrane is employed, the adhesive layer forming resin composition has a low viscosity. However, there is an advantage that the coating does not leak from the gaps between the fibers constituting the base fabric and the coating is easy regardless of the unevenness of the surface of the base fabric.
次に、防水膜上に保護膜を形成する。薄膜形成に適した公知の方法(例えば、ナイフコーティング法など)により、防水膜上に保護膜形成用樹脂組成物(ポリカーボネート系ポリウレタン樹脂、耐摩耗性向上剤、及び有機溶剤などを含む組成物)を塗布し、50〜150℃の温度で30秒〜5分間乾燥させることにより保護膜を形成し、本発明の積層布帛を得ることができる。その後、例えば150〜180℃の温度で、30秒〜3分間の熱処理を行ってもよい。 Next, a protective film is formed on the waterproof film. A resin composition for forming a protective film on a waterproof film (a composition containing a polycarbonate-based polyurethane resin, an abrasion resistance improver, an organic solvent, etc.) on a waterproof film by a known method suitable for thin film formation (for example, knife coating method). Is applied and dried at a temperature of 50 to 150 ° C. for 30 seconds to 5 minutes to form a protective film, whereby the laminated fabric of the present invention can be obtained. Then, you may perform the heat processing for 30 second-3 minutes, for example at the temperature of 150-180 degreeC.
本発明の積層布帛は、工業洗濯及び湿熱滅菌処理を繰り返した後においても、優れた血液・ウイルスバリア性及び耐剥離性が維持され、さらに、風合い、表面のタッチ感、耐摩耗性、及び外観品位にも優れるものである。そのため、医療用衣服・資材一般に好適であり、とりわけ手術衣、無菌衣、又は手術用ドレープなどに好適に用いられる。 The laminated fabric of the present invention maintains excellent blood / virus barrier properties and peeling resistance even after repeated industrial washing and wet heat sterilization treatment, and further, texture, surface touch, wear resistance, and appearance It is also excellent in quality. Therefore, it is suitable for medical clothes and materials in general, and is particularly suitable for surgical garments, aseptic garments, or surgical drapes.
以下、実施例に従って本発明を具体的に説明する。本発明はこの実施例に限定されない。 Hereinafter, the present invention will be described in detail according to examples. The present invention is not limited to this example.
(実施例1)
経糸及び緯糸としてポリエチレンテレフタレートマルチフィラメント(84dtex72f)を用い、2/2ツイル織物(経糸密度170本/2.54cm、緯糸密度100本/2.54cm)を製織した。この織物を日華化学株式会社の製精練剤「サンモールFL(商品名)」を1g/L使用して、80℃で20分間精練した。
Example 1
Polyethylene terephthalate multifilament (84 dtex 72f) was used as the warp and weft, and a 2/2 twill fabric (warp density 170 / 2.54 cm, weft density 100 / 2.54 cm) was woven. This fabric was scoured at 80 ° C. for 20 minutes using 1 g / L of a scouring agent “Sunmol FL (trade name)” manufactured by Nikka Chemical Co., Ltd.
精練後の織物をフッ素系撥水剤エマルジョンの水分散液(濃度6質量%)にパディングし、ウェットピックアップ率を40%に調整した後、乾燥させた。さらに170℃で40秒間熱処理させて、基布(厚み150μm)とした。 The scoured fabric was padded with an aqueous dispersion (concentration: 6% by mass) of a fluorine-based water repellent emulsion, the wet pick-up rate was adjusted to 40%, and then dried. Furthermore, it was heat-treated at 170 ° C. for 40 seconds to obtain a base fabric (thickness 150 μm).
次に、下記処方1の防水膜形成用樹脂組成物(粘度5000mPa・s/25℃、固形分質量21%)を調液し、経時で自然脱泡させた後、離型紙(リンテック株式会社製、「130TPD」)の離型面に、コンマコータにて70g/m2の塗布量で塗布した。次いで90℃で5分間乾燥させて、厚みが15μmの防水膜(ポリカーボネート系ポリウレタン樹脂100質量部に対して架橋アクリル微粒子を17質量部含有)を形成した。 Next, a waterproofing film forming resin composition (viscosity: 5000 mPa · s / 25 ° C., solid content: 21%) having the following formulation 1 was prepared and naturally degassed over time, and then a release paper (manufactured by Lintec Corporation). , “130TPD”) was applied at a coating amount of 70 g / m 2 with a comma coater. Subsequently, it was dried at 90 ° C. for 5 minutes to form a waterproof film having a thickness of 15 μm (containing 17 parts by mass of crosslinked acrylic fine particles with respect to 100 parts by mass of the polycarbonate-based polyurethane resin).
<処方1>
レザミンCUS−1500 100質量部
(大日精化工業株式会社製、固形分30質量%のポリカーボネート系ポリウレタン樹脂)
MR−7GC 5質量部
(綜研化学株式会社製、球状で平均粒子径6μmの架橋アクリル微粒子)
トルエン 45質量部
メチルエチルケトン 15質量部
<Prescription 1>
Resamine CUS-1500 100 parts by mass (manufactured by Dainichi Seika Kogyo Co., Ltd., polycarbonate-based polyurethane resin having a solid content of 30% by mass)
5 parts by mass of MR-7GC (manufactured by Soken Chemical Co., Ltd., spherical crosslinked acrylic fine particles having an average particle diameter of 6 μm)
Toluene 45 parts by weight Methyl ethyl ketone 15 parts by weight
次いで、基布と防水膜とを貼り合わせた。
詳しくは、まず下記処方2の接着剤層形成用樹脂組成物(粘度3500mPa・s/25℃、固形分52質量%)を調液した後、離型紙付き防水膜の防水膜表面に、コンマコータにて塗布量65g/m2にて塗布し、90℃で3分間乾燥させた。これにより、厚みが35μmの接着剤層を形成した(接着剤層の厚み/基布の厚み=7/30)。接着剤層と基布とを貼り合わせた後、温度80℃、圧力300kPaで熱圧着し、40℃で4日間の熟成を行って接着剤層を硬化させた。
Subsequently, the base fabric and the waterproof membrane were bonded together.
Specifically, first, after preparing a resin composition for forming an adhesive layer (viscosity 3500 mPa · s / 25 ° C., solid content 52 mass%) of the following formulation 2, on the waterproof membrane surface of the waterproof membrane with release paper, The coating amount was 65 g / m 2 and dried at 90 ° C. for 3 minutes. Thus, an adhesive layer having a thickness of 35 μm was formed (thickness of adhesive layer / thickness of base fabric = 7/30). After bonding the adhesive layer and the base fabric, thermocompression bonding was performed at a temperature of 80 ° C. and a pressure of 300 kPa, and aging was performed at 40 ° C. for 4 days to cure the adhesive layer.
<処方2>
ラックスキンUD4233−1 100質量部
(セイコー化成株式会社製、固形分60質量%のポリカーボネート系ポリウレタン樹脂)
U−4000 10質量部
(セイコー化成株式会社製、イソシアネート系硬化剤)
UY−5 1質量部
(セイコー化成株式会社製、ジオクチルチン系触媒)
メチルエチルケトン 12質量部
N,N−ジメチルホルムアミド 12質量部
<Prescription 2>
100 parts by mass of rack skin UD4233-1 (manufactured by Seiko Kasei Co., Ltd., polycarbonate-based polyurethane resin having a solid content of 60% by mass)
10 parts by mass of U-4000 (manufactured by Seiko Kasei Co., Ltd., isocyanate curing agent)
1 part by mass of UY-5 (manufactured by Seiko Kasei Co., Ltd., dioctyltin-based catalyst)
Methyl ethyl ketone 12 parts by mass N, N-dimethylformamide 12 parts by mass
硬化後に離型紙を剥離し、下記処方3の保護膜形成用樹脂組成物(粘度2500mPa・s/25℃、固形分20質量%)を調液し、防水膜表面に、ナイフコータにて、塗布量25g/m2で塗布した。次いで、100℃で3分間乾燥させることで、厚みが5μmの保護膜(ポリカーボネート系ポリウレタン樹脂100質量部に対して、耐摩耗性向上剤であるNε−ラウロイル−L−リジンの白色結晶性粉体及びKMR−3TAを、それぞれ10質量部含有)を形成した。続いて、170℃で1分間のセット加工を行い、実施例1の血液・ウイルスバリア性積層布帛を得た。 After curing, the release paper is peeled off, a protective film-forming resin composition (viscosity 2500 mPa · s / 25 ° C., solid content 20% by mass) of the following formulation 3 is prepared, and the coating amount is applied to the waterproof film surface with a knife coater. Application was at 25 g / m 2 . Next, by drying at 100 ° C. for 3 minutes, a protective film having a thickness of 5 μm (a white crystalline powder of N ε -lauroyl-L-lysine which is an abrasion resistance improver with respect to 100 parts by mass of the polycarbonate-based polyurethane resin) Body and KMR-3TA each containing 10 parts by mass). Subsequently, set processing was performed at 170 ° C. for 1 minute to obtain a blood / virus barrier laminate fabric of Example 1.
<処方3>
レザミンCUS−1500 100質量部
(大日精化工業株式会社製、固形分30質量%のポリカーボネート系ポリウレタン樹脂)
アミホープLL 3質量部
(味の素株式会社製、耐摩耗性向上剤としての薄片状Nε−ラウロイル−L−リジンの白色結晶性粉体)
KMR−3TA 3質量部
(綜研化学株式会社製、耐摩耗性向上剤としての球状で平均粒子径3μmの架橋アクリル微粒子)
メチルエチルケトン 70質量部
<Prescription 3>
Resamine CUS-1500 100 parts by mass (manufactured by Dainichi Seika Kogyo Co., Ltd., polycarbonate-based polyurethane resin having a solid content of 30% by mass)
Amihope LL 3 parts by mass (Ajinomoto Co., Inc., white crystalline powder of flaky N ε -lauroyl-L-lysine as an abrasion resistance improver)
3 parts by mass of KMR-3TA (manufactured by Soken Chemical Co., Ltd., spherical crosslinked acrylic fine particles having an average particle diameter of 3 μm as an abrasion resistance improver)
70 parts by mass of methyl ethyl ketone
(実施例2)
経糸及び緯糸としてポリエチレンテレフタレートマルチフィラメント(44dtex48f)を用い、平組織織物(経糸密度160本/2.54cm、緯糸密度120本/2.54cm)を製織した。続いて、この織物を日華化学株式会社製の精練剤「サンモールFL(商品名)」1g/Lを使用し、80℃で20分間精練した。精練後の織物を、ダイスタージャパン株式会社製の分散染料「Dianix Blue UN−SE(商品名)」を0.5%omf使用して130℃で30分間染色した。
(Example 2)
Polyethylene terephthalate multifilament (44 dtex 48f) was used as the warp and weft, and a plain texture fabric (warp density 160 / 2.54 cm, weft density 120 / 2.54 cm) was woven. Subsequently, this fabric was scoured at 80 ° C. for 20 minutes using 1 g / L of a scouring agent “Sun Mall FL (trade name)” manufactured by Nikka Chemical Co., Ltd. The scoured fabric was dyed at 130 ° C. for 30 minutes using 0.5% omf of a disperse dye “Dianix Blue UN-SE (trade name)” manufactured by Dystar Japan.
染色後の織物をフッ素系撥水剤エマルジョンの水分散液(濃度7質量%)にパディングし、ウェットピックアップ率を30%に調整した後、乾燥した。さらに170℃で40秒間熱処理することで、基布(厚み70μm)を得た。 The dyed fabric was padded with an aqueous dispersion (concentration: 7% by mass) of a fluorinated water repellent emulsion, the wet pick-up rate was adjusted to 30%, and then dried. Furthermore, the base fabric (thickness 70 micrometers) was obtained by heat-processing at 170 degreeC for 40 second (s).
次に、下記処方4の防水膜形成用樹脂組成物(粘度4500mPa・s/25℃、固形分質量20%)を調液し、経時で自然脱泡させた後、離型紙(リンテック株式会社製、「130TPD」)の離型面にコンマコータにて塗布量50g/m2にて塗布した。次いで、90℃で5分間乾燥させて、厚みが11μmの防水膜(ポリカーボネート系ポリウレタン樹脂100質量部に対して架橋アクリル微粒子を10質量部含有)を形成した。
<処方4>
レザミンCUS−1500 100質量部
(大日精化工業株式会社製、固形分30質量%のポリカーボネート系ポリウレタン樹脂)
MR−2G 3質量部
(綜研化学株式会社製、球状で平均粒子径が1μmの架橋アクリル微粒子)
トルエン 50質量部
メチルエチルケトン 15質量部
Next, a waterproofing film forming resin composition (viscosity 4500 mPa · s / 25 ° C., solid content 20%) of the following formulation 4 was prepared and naturally degassed over time, and then a release paper (manufactured by Lintec Corporation). , “130TPD”) was applied with a comma coater at a coating amount of 50 g / m 2 . Subsequently, it was dried at 90 ° C. for 5 minutes to form a waterproof film having a thickness of 11 μm (containing 10 parts by mass of crosslinked acrylic fine particles with respect to 100 parts by mass of the polycarbonate-based polyurethane resin).
<Prescription 4>
Resamine CUS-1500 100 parts by mass (manufactured by Dainichi Seika Kogyo Co., Ltd., polycarbonate-based polyurethane resin having a solid content of 30% by mass)
3 parts by mass of MR-2G (manufactured by Soken Chemical Co., Ltd., spherical crosslinked acrylic fine particles having an average particle diameter of 1 μm)
Toluene 50 parts by weight Methyl ethyl ketone 15 parts by weight
続いて、基布と防水膜とを貼り合わせた。
まず、下記処方5の接着剤形成用樹脂組成物(粘度2500mPa・s/25℃、固形分濃度48質量%)を調液し、離型紙付き防水膜の防水膜表面にコンマコータにて塗布量55g/m2にて塗布し、90℃で3分間の乾燥により、厚みが20μmの接着剤層(接着剤層の厚み/基布の厚み=2/7)を形成した。その後、接着剤層を介して基布と防水膜とを積層し、温度80℃、圧力300kPaで熱圧着し、40℃で3日間の熟成を行い、接着剤層を硬化させた。
Subsequently, the base fabric and the waterproof membrane were bonded together.
First, a resin composition for forming an adhesive of the following formulation 5 (viscosity 2500 mPa · s / 25 ° C., solid content concentration 48 mass%) was prepared, and applied to a waterproof membrane surface of a waterproof membrane with a release paper by a comma coater in an amount of 55 g. / was applied using m 2, drying of 3 minutes at 90 ° C., the thickness was formed adhesive layer of 20μm (thickness = 2/7 thick / base fabric of the adhesive layer). Thereafter, the base fabric and the waterproof membrane were laminated through the adhesive layer, thermocompression bonded at a temperature of 80 ° C. and a pressure of 300 kPa, and aged for 3 days at 40 ° C. to cure the adhesive layer.
<処方5>
ラックスキンUD4233−1 100質量部
(セイコー化成株式会社製、固形分60質量%のポリカーボネート系ポリウレタン樹脂)
U-4000 10質量部
(セイコー化成株式会社製、イソシアネート系硬化剤)
UY−5 1質量部
(セイコー化成株式会社製、ジオクチルチン系触媒)
メチルエチルケトン 20質量部
N,N−ジメチルホルムアミド 15質量部
次いで硬化後に離型紙を剥離した後、実施例1と同様の手法により保護膜(厚み5μm)を形成し、実施例2の血液・ウイルスバリア性積層布帛を得た。
<Prescription 5>
100 parts by mass of rack skin UD4233-1 (manufactured by Seiko Kasei Co., Ltd., polycarbonate-based polyurethane resin having a solid content of 60% by mass)
10 parts by mass of U-4000 (manufactured by Seiko Kasei Co., Ltd., isocyanate curing agent)
1 part by mass of UY-5 (manufactured by Seiko Kasei Co., Ltd., dioctyltin-based catalyst)
Methyl ethyl ketone 20 parts by mass N, N-dimethylformamide 15 parts by mass After the release paper was peeled after curing, a protective film (thickness 5 μm) was formed in the same manner as in Example 1, and the blood / virus barrier properties of Example 2 A laminated fabric was obtained.
(実施例3)
処方3の保護膜形成用樹脂組成物を、下記処方6(粘度4000mPa・s/25℃、固形分21質量%)の保護膜形成用樹脂組成物に変えて、厚みが6μmの保護膜(ポリカーボネート系ポリウレタン樹脂100質量部に対して、ポリテトラフルオロエチレン微粒子を27質量部含有)を形成した以外は、実施例2と同様の手法により、実施例3の血液・ウイルスバリア性積層布帛を得た。
(Example 3)
The protective film-forming resin composition of the prescription 3 was changed to a protective film-forming resin composition of the following prescription 6 (viscosity 4000 mPa · s / 25 ° C., solid content 21 mass%), and a protective film (polycarbonate) having a thickness of 6 μm The blood / virus barrier laminate fabric of Example 3 was obtained in the same manner as in Example 2 except that 27 parts by mass of polytetrafluoroethylene fine particles were contained per 100 parts by mass of the polyurethane resin. .
<処方6>
レザミンCUS−1500 100質量部
(大日精化工業株式会社製、固形分30質量%のポリカーボネート系ポリウレタン樹脂)
Fluon L173JE 8質量部
(旭硝子株式会社製、耐摩耗性向上剤としての一次粒子径0.2μmのポリテトラフルオロエチレン微粒子)
トルエン 60質量部
メチルエチルケトン 20質量部
<Prescription 6>
Resamine CUS-1500 100 parts by mass (manufactured by Dainichi Seika Kogyo Co., Ltd., polycarbonate-based polyurethane resin having a solid content of 30% by mass)
8 parts by mass of Fluon L173JE (manufactured by Asahi Glass Co., Ltd., polytetrafluoroethylene fine particles having a primary particle diameter of 0.2 μm as an abrasion resistance improver)
Toluene 60 parts by weight Methyl ethyl ketone 20 parts by weight
(実施例4)
処方6の保護膜形成用樹脂組成物の塗布量を55g/m2に変更し、厚みが12μmの保護膜を形成した以外は、実施例3と同様の手法により、実施例4の積層布帛を得た。
(Example 4)
The laminated fabric of Example 4 was prepared in the same manner as in Example 3 except that the coating amount of the resin composition for forming a protective film in Formulation 6 was changed to 55 g / m 2 and a protective film having a thickness of 12 μm was formed. Obtained.
(比較例1)
実施例1において、処方2の接着剤層形成用樹脂組成物の塗布量を20g/m2に変更し、接着剤層の厚みを11μmとした以外は、実施例1と同様の手法により、比較例1の積層布帛を得た。
(Comparative Example 1)
In Example 1, the coating amount of the resin composition for forming the adhesive layer in Formulation 2 was changed to 20 g / m 2 and the thickness of the adhesive layer was changed to 11 μm. The laminated fabric of Example 1 was obtained.
(比較例2)
実施例1において、処方2の接着剤層形成用樹脂組成物の塗布量を100g/m2に変更し、接着剤層の厚みを55μmとした以外は、実施例1と同様の手法により、比較例2の積層布帛を得た。
(Comparative Example 2)
In Example 1, the coating amount of the resin composition for forming an adhesive layer in Formulation 2 was changed to 100 g / m 2 and the thickness of the adhesive layer was changed to 55 μm. The laminated fabric of Example 2 was obtained.
(比較例3)
実施例1において、処方1の防水膜形成用樹脂組成物の塗布量を20g/m2に変更し、防水膜の厚みを5μmとした以外は、実施例1と同様の手法により、比較例3の積層布帛を得た。
(Comparative Example 3)
In Example 1, Comparative Example 3 was carried out in the same manner as in Example 1 except that the coating amount of the resin composition for forming a waterproof film in Formula 1 was changed to 20 g / m 2 and the thickness of the waterproof film was changed to 5 μm. A laminated fabric was obtained.
(比較例4)
実施例1において、処方1の防水膜形成用樹脂組成物の塗布量を110g/m2に変更し、防水膜の厚みを25μmとした以外は、実施例1と同様の手法により、比較例4の積層布帛を得た。
(Comparative Example 4)
In Example 1, Comparative Example 4 was carried out in the same manner as in Example 1 except that the coating amount of the resin composition for forming a waterproof film in Formulation 1 was changed to 110 g / m 2 and the thickness of the waterproof film was 25 μm. A laminated fabric was obtained.
(比較例5)
実施例1において、処方1の防水膜形成用樹脂組成物においてMR−7GC(架橋アクリル微粒子)を用いずに防水膜を形成しようとした。しかし、タック感が強過ぎて巻き取れなかったため、その後の工程に付することができず、積層布帛を得ることができなかった。
(Comparative Example 5)
In Example 1, an attempt was made to form a waterproof film without using MR-7GC (crosslinked acrylic fine particles) in the resin composition for forming a waterproof film of Formulation 1. However, the tackiness was so strong that it could not be wound, so that it could not be subjected to the subsequent steps, and a laminated fabric could not be obtained.
(比較例6)
実施例1において、処方1の防水膜形成用樹脂組成物におけるMR−7GC(架橋アクリル微粒子)の含有量を10質量部に変更し、防水膜(ポリカーボネート系ポリウレタン樹脂100質量部に対して架橋アクリル微粒子を33質量部含有)形成した以外は、実施例1と同様の手法により、比較例6の積層布帛を得た。
(Comparative Example 6)
In Example 1, the content of MR-7GC (crosslinked acrylic fine particles) in the resin composition for forming a waterproof film of Formulation 1 was changed to 10 parts by mass, and the waterproof film (crosslinked acrylic with respect to 100 parts by mass of the polycarbonate polyurethane resin) was used. A laminated fabric of Comparative Example 6 was obtained in the same manner as in Example 1 except that 33 parts by mass of fine particles were formed.
(比較例7)
実施例2において、保護膜を形成しなかった以外は実施例2と同様の手法により、比較例7の積層布帛を得た。
(Comparative Example 7)
A laminated fabric of Comparative Example 7 was obtained in the same manner as in Example 2 except that the protective film was not formed in Example 2.
(比較例8)
処方6の保護膜形成用樹脂組成物において、Fluon L173JE(耐摩耗向上剤)の含有量を2質量部に変更し、保護膜(ポリカーボネート系ポリウレタン樹脂100質量部に対して耐摩耗向上剤を7質量部含有)を形成した以外は、実施例2と同様の手法により、比較例8の積層布帛を得た。
(Comparative Example 8)
In the resin composition for forming a protective film of Formula 6, the content of Fluon L173JE (antiwear improver) was changed to 2 parts by mass, and the antiwear agent was added to 100 parts by mass of the protective film (polycarbonate polyurethane resin). A laminated fabric of Comparative Example 8 was obtained in the same manner as in Example 2 except that (part by mass) was formed.
(比較例9)
処方6の保護膜形成用樹脂組成物において、Fluon L173JEの量を12質量部に変更し、保護膜(ポリカーボネート系ポリウレタン樹脂100質量部に対して耐摩耗向上剤を40質量部含有)を形成した以外は、実施例2と同様の方法により、比較例9の積層布帛を得た。
(Comparative Example 9)
In the protective film-forming resin composition of the prescription 6, the amount of Fluon L173JE was changed to 12 parts by mass to form a protective film (containing 40 parts by mass of an antiwear agent for 100 parts by mass of the polycarbonate-based polyurethane resin). A laminated fabric of Comparative Example 9 was obtained in the same manner as in Example 2 except that.
(比較例10)
処方2の接着剤層形成用樹脂組成物において、U−4000(イソシアネート系硬化剤)を含有させなかった以外は、実施例1と同様の手法により、比較例10の積層布帛を得た。
(Comparative Example 10)
A laminated fabric of Comparative Example 10 was obtained in the same manner as in Example 1 except that U-4000 (isocyanate-based curing agent) was not contained in the resin composition for forming an adhesive layer of Formulation 2.
実施例及び比較例で得られた積層布帛について、以下の方法による連続処理を行い、各々の物性を測定又は評価した。
[工業洗濯]
工業洗濯機(株式会社大栄科学精器製作所製、型式;WS−1SE)を用いて、標準的な1回分の洗濯条件「73℃×20分間」を下記条件に変更し、10回分の洗濯とした。
浴比;1:40(1.5kg:60L)
洗剤;ピュア−石鹸(株式会社不動化学製)1g/L、苛性ソーダ0.08g/Lを添加し、pH値を10に調整したものを用いた。
工程;洗い(73℃×200分間)→湯洗(40℃×30分間)→オーバーフローすすぎ(常温×15分間)→脱水→タンブル乾燥(60℃×20分間)
About the laminated fabric obtained by the Example and the comparative example, the continuous process by the following method was performed and each physical property was measured or evaluated.
[Industrial laundry]
Using an industrial washing machine (manufactured by Daiei Kagaku Seiki Seisakusho Co., Ltd., model: WS-1SE), the standard washing conditions for one wash “73 ° C. × 20 minutes” were changed to the following conditions, did.
Bath ratio; 1:40 (1.5 kg: 60 L)
Detergent: Pure soap (manufactured by Fudo Chemical Co., Ltd.) 1 g / L, caustic soda 0.08 g / L were added, and the pH value was adjusted to 10.
Process: Washing (73 ° C. × 200 minutes) → Washing water (40 ° C. × 30 minutes) → Overflow rinsing (normal temperature × 15 minutes) → Dehydration → Tumble drying (60 ° C. × 20 minutes)
[湿熱滅菌処理]
高圧蒸気滅菌器(株式会社平山製作所製、「HV50型」)を用いて、標準的な1回分の滅菌条件「135℃×8分間」を「135℃×80分間」に変更し、10回分の湿熱滅菌処理とした。
[Moist heat sterilization]
Using a high-pressure steam sterilizer (“HV50 type” manufactured by Hirayama Seisakusho Co., Ltd.), the standard one-time sterilization condition “135 ° C. × 8 minutes” is changed to “135 ° C. × 80 minutes”, and 10 times Wet heat-sterilization treatment.
[連続処理]
前記工業洗濯10回分と前記湿熱滅菌処理10回分との連続処理を、1サイクル(10回分)として処理を行った。
[Continuous processing]
The treatment was carried out with a continuous treatment of 10 times of the industrial washing and 10 times of the wet heat sterilization treatment as one cycle (10 times).
(1)耐水圧(防水性の耐久性)
JIS L 1092(高水圧法)に基づいて測定した。なお、防水性の耐久性評価を、10サイクル処理後の耐水圧の値により行った。
(1) Water pressure resistance (waterproof durability)
It measured based on JIS L 1092 (high water pressure method). In addition, waterproof durability evaluation was performed by the value of the water pressure resistance after 10 cycle processing.
(2)耐摩耗性
JIS L 0849に従って評価した。試験片を幅15cmかつ長さ30cmの大きさに切り出し、摩擦試験機2型の試験片台上に平行に取り付け、4辺をガムテープで固定した。擦子先端に綿布(JIS L 0803規定の3号綿布)を装着して、1.96Nの力で保護膜表面を500回摩耗し、下記基準に基づいて目視評価した。
◎:摩耗損傷がほとんど目立たない。
○:摩耗損傷が少し目立つ。
△:摩耗損傷しているものの、大きく目立つ損傷は認められない。
△−×:損傷が目立つ。
×:摩耗損傷が大きく、膜に穴があくほどの損傷が認められる。
(2) Abrasion resistance It evaluated according to JISL0849. The test piece was cut into a size of 15 cm in width and 30 cm in length, and mounted in parallel on a test piece base of a friction tester type 2, and four sides were fixed with gummed tape. A cotton cloth (No. 3 cotton cloth defined in JIS L 0803) was attached to the tip of the scraper, and the surface of the protective film was worn 500 times with a force of 1.96 N, and visually evaluated based on the following criteria.
A: Wear damage is hardly noticeable.
○: Abrasion damage is slightly noticeable.
(Triangle | delta): Although abrasion damage is carried out, the conspicuous damage is not recognized.
Δ-x: Damage is conspicuous.
X: Abrasion damage is large and damage to the extent that the film has a hole is recognized.
(3)風合い
得られた積層布帛に対しハンドリングにて、下記基準に基づいて評価した。
◎:ラミネート商品でありながら風合いが極めて良好である。
○:ラミネート商品でありながら風合いが良好である。
△:ラミネート商品として風合いが普通である。
△-×:ラミネート商品としてやや硬い。
×:ラミネート商品としては硬く、明らかに風合いに劣っている
(3) Texture The obtained laminated fabric was evaluated by handling based on the following criteria.
A: Although it is a laminate product, the texture is extremely good.
○: The texture is good while being a laminated product.
Δ: The texture is normal as a laminate product.
Δ- ×: Slightly hard as a laminate product.
×: Hard as a laminated product, clearly inferior in texture
(4)外観品位
得られた積層布帛の保護膜面の外観を、下記基準に基づいて評価した。
○:外観品位が極めて良好。
△:外観品位が良好。
×:塗布筋が目立つ。
(4) Appearance quality The appearance of the protective film surface of the obtained laminated fabric was evaluated based on the following criteria.
○: Appearance quality is very good.
Δ: Appearance quality is good.
X: Application | coating stripe is conspicuous.
(5)連続処理後の剥離状況(耐剥離性)
10サイクル(10Cとも表記する)の連続処理を行い、下記基準に基づき目視判定し、耐剥離性の評価とした。
◎:剥離なし。
○:部分的に少し剥離した。
△:部分的に剥離した。
△−×:ほぼ全面剥離した。
×:全面剥離した。
(5) Peeling status after continuous treatment (peeling resistance)
A continuous treatment of 10 cycles (also referred to as 10C) was performed, and visual judgment was made based on the following criteria to evaluate peeling resistance.
A: No peeling.
○: Partially peeled off.
Δ: Partially peeled off.
Δ-x: almost peeled off.
X: The entire surface was peeled off.
(6)人工血液バリア性
ASTM F 1670−08B法に基づいて評価した。本発明においては10サイクル後の判定が合格であれば実用に十分耐え得るものであり、好ましいと評価した。
(6) Artificial blood barrier property It evaluated based on ASTMF1670-08B method. In the present invention, if the judgment after 10 cycles is acceptable, it can be sufficiently put into practical use and evaluated as preferable.
(7)ウイルスバリア性
ASTM F 1671−07B法に基づいて評価した。本発明においては、10サイクル後の判定が合格であれば実用に十分耐え得るものであり、好ましいと評価した。
(7) Virus barrier property It evaluated based on ASTMF1671-07B method. In the present invention, if the determination after 10 cycles is acceptable, it can be sufficiently put into practical use and evaluated as preferable.
表1から明らかなように、実施例1〜4で得られた本発明の積層布帛は、防水性、耐摩耗性、耐剥離性、風合い、外観品位、及び血液・ウイルスバリア性の耐久性の全てにおいて良好であった。特に、実施例2及び実施例3の積層布帛は、基布、防水膜及び接着剤層の厚みをより薄くしたため特に風合いに極めて優れていた。実施例3及び4の積層布帛は、保護膜を厚くし、さらに耐磨耗性向上剤としてポリテトラフルオロエチレン微粒子を用いたため耐摩耗性に顕著に優れていた。 As is apparent from Table 1, the laminated fabrics of the present invention obtained in Examples 1 to 4 have waterproofness, abrasion resistance, peel resistance, texture, appearance quality, and blood / virus barrier durability. All were good. In particular, the laminated fabrics of Example 2 and Example 3 were extremely excellent in texture because the thickness of the base fabric, waterproof membrane and adhesive layer was made thinner. The laminated fabrics of Examples 3 and 4 were remarkably excellent in abrasion resistance because the protective film was thickened and polytetrafluoroethylene fine particles were used as an abrasion resistance improver.
比較例1の積層布帛は、接着剤層の厚みが過小であったため、6C目の工業洗濯中に全剥離した。比較例2の積層布帛は、接着剤層の厚みが過大であったために耐久性に劣り、10C後の工業洗濯及び湿熱滅菌処理後のウイルスバリア性に劣り、さらに風合いにも劣っていた。 The laminated fabric of Comparative Example 1 was completely peeled off during the 6C industrial washing because the thickness of the adhesive layer was too small. The laminated fabric of Comparative Example 2 was inferior in durability because of the excessive thickness of the adhesive layer, inferior in virus barrier properties after industrial washing and wet heat sterilization after 10 C, and inferior in texture.
比較例3の積層布帛は、防水膜の厚みが過小であったために防水性に劣り、さらに10C後の工業洗濯及び湿熱滅菌処理後の血液・ウイルスバリア性にも劣っていた。比較例4の積層布帛は、防水膜の厚みが過大であったために耐久性に劣り、10C後の工業洗濯及び湿熱滅菌処理後のウイルスバリア性に劣り、風合いにも劣っていた。 The laminated fabric of Comparative Example 3 was inferior in waterproofness because the waterproof membrane was too thin, and was also inferior in blood / virus barrier properties after industrial washing and wet heat sterilization after 10C. The laminated fabric of Comparative Example 4 was inferior in durability due to the excessive thickness of the waterproof membrane, inferior in virus barrier properties after industrial washing and wet heat sterilization after 10C, and inferior in texture.
比較例6の積層布帛は、防水膜における架橋アクリル微粒子の含有量が過多であったために、高耐水圧が達成されているものの、凝集物が発生したことで膜破損が発生し、10C後の工業洗濯及び湿熱滅菌処理後のウイルスバリア性に劣り、さらに風合いにも劣っていた。 In the laminated fabric of Comparative Example 6, since the content of the crosslinked acrylic fine particles in the waterproof membrane was excessive, high water pressure resistance was achieved, but membrane breakage occurred due to the occurrence of aggregates, and after 10C The virus barrier property after industrial washing and wet heat sterilization was inferior, and the texture was also inferior.
比較例7の積層布帛は、保護膜が形成されていなかったために、防水性、耐摩耗性、耐剥離性、耐久性に劣り、10C後の工業洗濯及び湿熱滅菌処理後の人工血液・ウイルスバリア性が不合格であった。比較例8の積層布帛は、保護膜における耐摩耗向上剤の含有量が過少であったため耐摩耗性に劣り、さらに10C後の工業洗濯及び湿熱滅菌処理後の人工血液・ウイルスバリア性が不合格であり、加えてタッチ感にも乏しかった。 Since the laminated fabric of Comparative Example 7 was not formed with a protective film, it was inferior in waterproofness, abrasion resistance, peel resistance and durability, and artificial blood / virus barrier after industrial washing and wet heat sterilization after 10C Sex was rejected. The laminated fabric of Comparative Example 8 was inferior in wear resistance because the content of the antiwear improver in the protective film was too small, and also failed in artificial blood / virus barrier properties after 10C industrial washing and wet heat sterilization treatment In addition, the touch was poor.
比較例9の積層布帛は、10C後の工業洗濯及び湿熱滅菌処理後の人工血液・ウイルスバリア性は合格であったが、保護膜における耐摩耗向上剤の含有量が過多であったために外観品位、及び風合いに劣るものであった。 The laminated fabric of Comparative Example 9 passed the artificial laundry / virus barrier property after industrial washing and wet heat sterilization after 10 C, but the appearance quality was high because the content of the anti-wear improver in the protective film was excessive. , And the texture was inferior.
比較例10の積層布帛、接着剤層に含まれる接着剤が硬化型ではなかったために耐久性に劣り、2C目の工業洗濯処理中に剥離してしまい、その後の評価に付することができなかった。 Since the adhesive contained in the laminated fabric and the adhesive layer of Comparative Example 10 was not curable, it was inferior in durability and peeled off during the 2C industrial washing process, and could not be subjected to subsequent evaluation. It was.
1 血液・ウイルスバリア性積層布帛
2 基布
3 接着剤層
4 防水膜
5 保護膜
1 Blood / Virus Barrier Laminated Fabric 2 Base Fabric 3 Adhesive Layer 4 Waterproof Film 5 Protective Film
Claims (6)
前記接着剤層はポリカーボネート系ポリウレタン樹脂を主成分として含有する硬化型接着剤を含み、かつ厚みが15〜50μmであり、
前記防水膜はポリカーボネート系ポリウレタン樹脂100質量部、及び架橋アクリル微粒子3〜30質量部を含有し、かつ厚みが7〜20μmであり、
前記保護膜はポリカーボネート系ポリウレタン樹脂100質量部、及び耐摩耗性向上剤8〜35質量部を含有することを特徴とする、血液・ウイルスバリア性積層布帛。 A blood / virus barrier laminate fabric in which an adhesive layer, a waterproof membrane and a protective membrane are laminated in this order on one side of a base fabric containing a polyester-based synthetic fiber,
The adhesive layer includes a curable adhesive containing a polycarbonate-based polyurethane resin as a main component, and has a thickness of 15 to 50 μm.
The waterproof membrane contains 100 parts by weight of a polycarbonate-based polyurethane resin and 3 to 30 parts by weight of crosslinked acrylic fine particles, and has a thickness of 7 to 20 μm.
The protective film contains 100 parts by mass of a polycarbonate-based polyurethane resin and 8 to 35 parts by mass of an abrasion resistance improver, and is a blood / virus barrier laminate fabric.
前記基布と前記防水膜とを、前記接着剤層で貼りあわせた後、前記防水膜上に前記保護膜を形成することを特徴とする、血液・ウイルスバリア性積層布帛の製造方法。
A method for producing the blood / virus barrier laminate fabric according to any one of claims 1 to 5,
A method for producing a blood / virus barrier laminate fabric, comprising: bonding the base fabric and the waterproof membrane together with the adhesive layer; and forming the protective film on the waterproof membrane.
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