US20120322328A1 - Moisture-permeable waterproof fabric - Google Patents
Moisture-permeable waterproof fabric Download PDFInfo
- Publication number
- US20120322328A1 US20120322328A1 US13/580,278 US201113580278A US2012322328A1 US 20120322328 A1 US20120322328 A1 US 20120322328A1 US 201113580278 A US201113580278 A US 201113580278A US 2012322328 A1 US2012322328 A1 US 2012322328A1
- Authority
- US
- United States
- Prior art keywords
- moisture
- polyurethane resin
- sebacic acid
- plant
- polyol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 239000004744 fabric Substances 0.000 title claims abstract description 53
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 claims abstract description 125
- 229920005749 polyurethane resin Polymers 0.000 claims abstract description 98
- 229920005862 polyol Polymers 0.000 claims abstract description 84
- 150000003077 polyols Chemical class 0.000 claims abstract description 84
- 229920005989 resin Polymers 0.000 claims abstract description 44
- 239000011347 resin Substances 0.000 claims abstract description 44
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 35
- 230000035699 permeability Effects 0.000 claims abstract description 34
- 238000000034 method Methods 0.000 claims description 32
- 239000012948 isocyanate Substances 0.000 claims description 26
- 150000002513 isocyanates Chemical class 0.000 claims description 26
- 150000002009 diols Chemical class 0.000 claims description 19
- 239000004970 Chain extender Substances 0.000 claims description 7
- 238000006243 chemical reaction Methods 0.000 claims description 5
- 239000003208 petroleum Substances 0.000 abstract description 11
- 239000000463 material Substances 0.000 abstract description 9
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 54
- 239000000243 solution Substances 0.000 description 31
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 26
- 239000000203 mixture Substances 0.000 description 17
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 16
- 230000003578 releasing effect Effects 0.000 description 16
- 239000004359 castor oil Substances 0.000 description 14
- 235000019438 castor oil Nutrition 0.000 description 14
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 14
- 238000000576 coating method Methods 0.000 description 13
- 239000000377 silicon dioxide Substances 0.000 description 13
- 239000011248 coating agent Substances 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 12
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 10
- 239000003795 chemical substances by application Substances 0.000 description 10
- 238000011156 evaluation Methods 0.000 description 9
- 229920002635 polyurethane Polymers 0.000 description 9
- 239000004814 polyurethane Substances 0.000 description 9
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 8
- 238000001035 drying Methods 0.000 description 8
- 238000007654 immersion Methods 0.000 description 8
- 239000012299 nitrogen atmosphere Substances 0.000 description 8
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 7
- 239000004677 Nylon Substances 0.000 description 7
- 230000007613 environmental effect Effects 0.000 description 7
- 229920001778 nylon Polymers 0.000 description 7
- 239000005871 repellent Substances 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- 239000007858 starting material Substances 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- 230000002209 hydrophobic effect Effects 0.000 description 6
- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical compound CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000000758 substrate Substances 0.000 description 5
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- 239000002202 Polyethylene glycol Substances 0.000 description 4
- 239000001361 adipic acid Substances 0.000 description 4
- 235000011037 adipic acid Nutrition 0.000 description 4
- 230000015271 coagulation Effects 0.000 description 4
- 238000005345 coagulation Methods 0.000 description 4
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 229920001223 polyethylene glycol Polymers 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 229920005672 polyolefin resin Polymers 0.000 description 3
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 238000003475 lamination Methods 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- 239000003495 polar organic solvent Substances 0.000 description 2
- 239000002798 polar solvent Substances 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920005906 polyester polyol Polymers 0.000 description 2
- WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 description 2
- 229960003656 ricinoleic acid Drugs 0.000 description 2
- FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 description 1
- 229940015975 1,2-hexanediol Drugs 0.000 description 1
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-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
- ZEMPKEQAKRGZGQ-AAKVHIHISA-N CCCCCCC(O)C/C=C\CCCCCCCC(=O)OCC(COC(=O)CCCCCCC/C=C\CC(O)CCCCCC)OC(=O)CCCCCCC/C=C\CC(O)CCCCCC Chemical compound CCCCCCC(O)C/C=C\CCCCCCCC(=O)OCC(COC(=O)CCCCCCC/C=C\CC(O)CCCCCC)OC(=O)CCCCCCC/C=C\CC(O)CCCCCC ZEMPKEQAKRGZGQ-AAKVHIHISA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-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
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- FHKSXSQHXQEMOK-UHFFFAOYSA-N hexane-1,2-diol Chemical compound CCCCC(O)CO FHKSXSQHXQEMOK-UHFFFAOYSA-N 0.000 description 1
- 239000012943 hotmelt Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-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
- 239000000314 lubricant Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- AYLRODJJLADBOB-QMMMGPOBSA-N methyl (2s)-2,6-diisocyanatohexanoate Chemical compound COC(=O)[C@@H](N=C=O)CCCCN=C=O AYLRODJJLADBOB-QMMMGPOBSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- FVXBCDWMKCEPCL-UHFFFAOYSA-N nonane-1,1-diol Chemical compound CCCCCCCCC(O)O FVXBCDWMKCEPCL-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000006353 oxyethylene group Chemical group 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000011846 petroleum-based material Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000747 poly(lactic acid) Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 239000004626 polylactic acid Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
- C08G18/76—Polyisocyanates or polyisothiocyanates cyclic aromatic
- C08G18/7657—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings
- C08G18/7664—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups
- C08G18/7671—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups containing only one alkylene bisphenyl group
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
- C08G18/4202—Two or more polyesters of different physical or chemical nature
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
- C08G18/4236—Polycondensates having carboxylic or carbonic ester groups in the main chain containing only aliphatic groups
- C08G18/4238—Polycondensates having carboxylic or carbonic ester groups in the main chain containing only aliphatic groups derived from dicarboxylic acids and dialcohols
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
- C08G18/78—Nitrogen
- C08G18/79—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates
- C08G18/791—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups
- C08G18/792—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups formed by oligomerisation of aliphatic and/or cycloaliphatic isocyanates or isothiocyanates
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
- C09D175/06—Polyurethanes from polyesters
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/77—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with silicon or compounds thereof
- D06M11/79—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with silicon or compounds thereof with silicon dioxide, silicic acids or their salts
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/564—Polyureas, polyurethanes or other polymers having ureide or urethane links; Precondensation products forming them
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
- D06M2200/10—Repellency against liquids
- D06M2200/12—Hydrophobic properties
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/20—Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
- Y10T442/2139—Coating or impregnation specified as porous or permeable to a specific substance [e.g., water vapor, air, etc.]
Definitions
- the present invention relates to a moisture-permeable waterproof fabric, particularly a moisture-permeable waterproof fabric which comprises a plant-based component and has equivalent or superior performance as compared to conventional petroleum-based polyurethane resins.
- polyurethane resins are widely employed for their excellent mechanical characteristics, and porous films of polyurethane resins prepared by a wet coagulation system and non-porous films of polyurethane resins having a hydrophilic group are utilized.
- the water pressure resistance (JIS L 1092 A method) of the wet-type porous film structure disclosed in the above-described Patent Literature is about 1,600 mmH 2 O and the water resistance is thus not sufficient from the standpoint of practical waterproofing.
- polylactic resins generally lack toughness, so that they become fragile and lack flexibility especially when they are made into a porous film. Thus, it is difficult to use a polylactic resin in apparel applications and the like.
- a polyol such as a castor oil or a modified castor oil, which is a plant-based component
- a polyol such as a castor oil or a modified castor oil, which is a plant-based component
- Unexamined Japanese Patent Application Kokai Publication No. 2009-149876 discloses a moisture-permeable polyurethane resin comprising a plant-based polymeric diol component produced from castor oil.
- this plant-based polymeric diol component in combination with a polymeric diol component containing an oxyethylene group which is a hydrophilic group, the resulting polyurethane resin is imparted with hydrophilicity in order to improve the moisture permeability.
- the hydrophilic polyurethane resin is not porous, so that there is a problem in that it is difficult to attain sufficient moisture permeability (JIS L-1099 A-1 method).
- castor oil is a composition mainly composed of fatty acid triglyceride and the principal component of the constituent fatty acid is ricinoleic acid; therefore, castor oil has about 2.7 hydroxyl groups per molecule. Yet, when a polyol having more than 2 hydroxyl groups per molecule is used, since a branched structure or a cross-linked structure is formed, the resulting polyurethane resin becomes overly hardened, so that a resin film satisfying practically appropriate flexibility (texture) cannot be obtained.
- dicarboxylic acid-based diols such as sebacic acid are known.
- a polyurethane resin produced by using a dicarboxylic acid-based diol for example, Unexamined Japanese Patent Application Kokai Publication No. H07-88833 discloses a moisture-permeable porous sheet material prepared by a wet coagulation system and JP 4329046B discloses a moisture curable-type hot melt film.
- the former does not have a practically sufficient level of moisture permeability and waterproof property; therefore, it has a problem of being not suitable as an outdoor sporting wear material where high moisture permeability and water-resistance are required.
- the latter is not suitable for mass production because of the complicated production process thereof and also has a problem in that, since the polyurethane resin has hydrophilic groups, the film has high water-swellability, which potentially causes a marked decrease in the strength upon contact with water or the like. Moreover, expression of moisture permeability, waterproof property, mechanical strength and the like in a polyurethane resin by these techniques is largely dependent on the components and additives constituting the polyurethane resin other than sebacic acid; therefore, there is a limitation in terms of designable structure.
- An object of the present invention is to solve the above-described problems, in particular, to provide a moisture-permeable waterproof fabric which comprises a plant-based component contributing to a reduction in environmental load and exhibits equivalent or superior performance as compared to a case where a conventional petroleum-based polyurethane resin is used.
- the present inventors intensively studied to discover that the above-described problems can be solved by using, as a starting material of a polyurethane resin, a sebacic acid-based polyol-component which is produced from sebacic acid obtained from castor oil or the like as a plant-based component, thereby completing the present invention.
- the present invention relates to a moisture-permeable waterproof fabric which comprises, on at least one surface thereof, a porous resin film composed of a polyurethane resin containing 5 to 80% by weight of a sebacic acid-based polyol component produced from a plant-based sebacic acid, wherein the moisture permeability measured by the JIS L1099 A-1 method and the moisture permeability measured by the JIS L1099 B-1 method are both not less than 5,000 g/m 2 ⁇ 24 h and the water pressure resistance measured by the JIS L-1092 B method (high water pressure method) is not lower than 5,000 mmH 2 O.
- the above-described polyurethane resin is produced from at least a polyol component, an isocyanate component and a chain extender component and the molar ratio of the polyol component and the isocyanate component, polyol/isocyanate, is preferably between 1/6 and 1/2.
- the above-described sebacic acid-based polyol-component is preferably an ⁇ , ⁇ -diol which is produced by a reaction of a plant-based sebacic acid and a diol and has a number average molecular weight of 500 to 5,000.
- the toughness which is a problem of using a plant-based resin such as polylactic acid resin, can be improved and an equivalent toughness as that of a polyurethane resin comprising a petroleum-based component can be attained.
- a moisture permeability and waterproof performance equivalent or superior to a moisture-permeable waterproof fabric produced from a polyurethane resin comprising an existing petroleum-based component can be provided.
- the moisture-permeable waterproof fabric of the present invention can contribute to a reduction in environmental load.
- the moisture-permeable waterproof fabric according to the present invention is characterized in that it comprises, on at least one surface thereof, a porous resin film composed of a polyurethane resin containing 5 to 80% by weight of a sebacic acid-based polyol component produced from a plant-based sebacic acid and that the moisture permeability measured by the JIS L1099 A-1 method and the moisture permeability measured by the JIS L1099 B-1 method are both not less than 5,000 g/m 2 ⁇ 24 h and the water pressure resistance measured by the JIS L-1092 B method (high water pressure method) is not lower than 5,000 mmH 2 O.
- the sebacic acid used in the present invention is, for example, a C 10 linear saturated dibasic acid obtained by a cleavage reaction of a vegetable oil such as castor oil by a caustic alkali.
- a vegetable oil such as castor oil by a caustic alkali.
- those commercially available castor oil-based polyols are produced from ricinoleic acid obtained by saponification decomposition of castor oil and are, therefore, different from those polyols produced from sebacic acid.
- the material oil of the plant-based sebacic acid is not particularly restricted to castor oil.
- Castor oil is a compound mainly having the structure represented by the following formula 1.
- sebacic acid is a dicarboxylic acid having the structure represented by the following formula 2.
- Sebacic acid-based polyols are, as an alternative to polyester polyols and the like, used as a starting material of urethane used as an adhesive or a paint; however, in the present invention, it was discovered that a polyurethane resin produced by using sebacic acid as a starting material has high permeability and waterproof property as well as excellent toughness and such polyurethane resin was used as a principal material of a resin film of a moisture-permeable waterproof fabric.
- the sebacic acid-based polyol used in the present invention is preferably a sebacic acid-based polyester diol obtained by a reaction of a plant-based sebacic acid and a diol.
- the upper limit of the number of carbon atoms in the diol is not particularly restricted; however, the number average molecular weight of the resulting sebacic acid-based polyol is in the range of preferably 500 to 5,000, more preferably 1,000 to 3,000. When the number average molecular weight is smaller than 500, the resulting polyurethane resin tends to be too hard, while when it is greater than 5,000, the resulting polyurethane resin tends to be too soft.
- diol to be reacted with sebacic acid examples include diols such as ethylene glycol, propanediol, hexanediol, nonanediol, neopentyl glycol and polyethylene glycol (PEG). These diols may be used individually, or two or more thereof may be used in combination as required.
- a plant-based component be used also in the diol per se to be reacted with sebacic acid.
- the plant-based percentage of the polyol component is 100%.
- the amount of the plant-based component(s) contained in the polyurethane resin is preferably 5 to 80% by weight, more preferably 6 to 75% by weight.
- the amount of the plant-based component(s) is less than 5% by weight, the environmental load-reducing effect tends to be small, while when the amount is greater than 80% by weight, a polyurethane resin having sufficiently satisfactory moisture permeability, waterproof property, mechanical strength and the like may not be obtained and it may become difficult to obtain a porous resin film.
- the content of the sebacic acid-based polyol component obtained from a plant-based sebacic acid in a polyurethane-forming material is 5 to 80% by weight, preferably 6 to 75% by weight.
- the percentage of the above-described polyol component is preferably greater from the standpoint of environmental load; however, when it is greater than 80% by weight, it may become difficult to form a film or obtain a porous resin film, so that a polyurethane resin having sufficiently satisfactory moisture permeability, waterproof property, mechanical strength and the like may not be obtained.
- the amount of the above-described polyol component is less than 5% by weight, the plant-based percentage of the resulting polyurethane resin is reduced; therefore, such an amount is not preferred from the standpoint of reducing environmental load.
- a polyol composed of an aliphatic dicarboxylic acid which is normally used in the production of polyurethane
- a polyol composed of a C 4 to C 12 dicarboxylic acid is commonly employed; however, since sebacic acid contains a greater number of carbon atoms as compared to adipic acid and the like commonly used as a starting material of a polyurethane resin, a polyurethane resin produced from a sebacic acid-based polyol can be expected to have an improved waterproof property.
- a polyurethane resin produced from the above-described polyol can be expected to have a good balance of the hydrophobicity and the mechanical strength, as well as an improved moisture permeability because of the porous film-forming property.
- the amount of the above-described polyol component is less than 5% by weight, these effects may not be sufficiently attained; therefore, such an amount is not preferred.
- composition percentage of the sebacic acid-based polyol component used herein relates to the percentage of all sebacic acid-based polyols produced from a plant-based sebacic acid, irrespective of the type thereof.
- the polyol component of polyurethane resin used in the present invention one produced from a dicarboxylic acid other than sebacic acid may also be used in combination.
- the dicarboxylic acid other than sebacic acid include dicarboxylic acids such as adipic acid, succinic acid, terephthalic acid and isophthalic acid that are derived from petroleum.
- the amount of these carboxylic acids to be used is preferably small in order not to reduce the plant-based percentage; however, it is set as appropriate with consideration of the above-described composition percentage and the later-described molar ratio of the polyol component and the isocyanate component.
- dihydric polyol in addition to the above-described plant-based polyol, other dihydric polyol may also be used in combination.
- specific examples thereof include petroleum-based dihydric polyols such as polyester polyols, polyether polyols, polycarbonate polyols, polyamide-based polyols, silicone-based polyols and fluorine-based polyols.
- these dihydric polyols are preferably added in the smallest amount possible.
- the molar ratio of the polyol component and the isocyanate component, polyol/isocyanate is preferably between 1/6 and 1/2, more preferably between 1/5.5 and 1/2.5.
- the amount of the isocyanate component is excessive, it tends to be difficult to control the reaction, while when the amount of the polyol component is excessive, it tends to be difficult to obtain a porous resin film.
- the NCO/OH equivalent ratio of the isocyanate component, polyol component and chain extender component is usually 0.95 to 1.15, preferably substantially 1.
- the NCO/OH equivalent ratio is not in this range, a polyurethane resin having a high molecular weight cannot be obtained, so that it tends to be difficult to produce a moisture-permeable waterproof fabric having useful performance.
- the number average molecular weight of the polyurethane resin used in the present invention is preferably between 50,000 and 500,000.
- a resin or resin solution suitable for coating and the like in the formation of a resin film cannot be obtained and it tends to be difficult to obtain a resin film which exhibits practical moisture permeability and water-resistance.
- a conventional prepolymer method can be employed as a method for obtaining a polyurethane resin.
- a method in which a prepolymer is prepared by allowing the above-described polyol and isocyanate to react in a solvent inert to isocyanate group for example, a polar organic solvent such as dimethylformamide (DMF) or dimethyl sulfoxide (DMSO) or a non-polar organic solvent such as methyl ethyl ketone (MEK), toluene or xylene, and then the thus obtained prepolymer is allowed to react with a chain extender such as a diol to increase the degree of polymerization
- a chain extender such as a diol
- the isocyanate component used in the present invention is not particularly restricted; however, examples thereof include diisocyanates represented by aromatic diisocyanates such as xylene diisocyanate, 4,4′-diphenylmethane diisocyanate (MDI) and 2,4- and/or 2,6-tolylene diisocyanate; aliphatic diisocyanates such as hexamethylene diisocyanate and lysine diisocyanate; and alicyclic diisocyanates such as tetramethylene diisocyanate, isophorone diisocyanate and hydrogenated MDI. These isocyanates may be used individually, or two or more thereof may be used in combination as required.
- aromatic diisocyanates such as xylene diisocyanate, 4,4′-diphenylmethane diisocyanate (MDI) and 2,4- and/or 2,6-tolylene diisocyanate
- aliphatic diisocyanates such as hexam
- the chain extender component is not particularly restricted; however, generally, a diol having a relatively low molecular weight is employed.
- diol examples include ethylene glycol, diethylene glycol, propanediol, butanediol, hexanediol and polyethylene glycol (PEG) that are derived from petroleum; and 1,3-propanediol and 1,2-hexanediol that are derived from a plant. These diols may be used individually, or two or more thereof may be used in combination as required.
- a diamine and/or the like may also be used as required.
- the chain extender is generally used primarily for controlling the molecular weight and physical properties of the resulting film in the synthesis of a resin used as a moisture-permeable waterproof film.
- the above-described polyurethane resin may be used by diluting it with an organic solvent or the like as required. Further, to the above-described polyurethane resin, an antioxidant, a stabilizer such as a light resistance-improving agent, an inorganic filler, a non-solvent, a lubricant, a water repellant, a pigment, other additive(s) and/or a function-imparting agent may also be added as appropriate.
- an antioxidant such as a light resistance-improving agent, an inorganic filler, a non-solvent, a lubricant, a water repellant, a pigment, other additive(s) and/or a function-imparting agent may also be added as appropriate.
- the moisture-permeable waterproof fabric according to the present invention comprises the above-described polyurethane resin on at least one surface thereof and within the moisture-permeable waterproof fabric, the moisture permeability measured by the JIS L1099 A-1 method and the moisture permeability measured by the JIS L1099 B-1 method are both not less than 5,000 g/m 2 ⁇ 24 h and the water pressure resistance measured by the JIS L1092 B method (high water pressure method) is not lower than 5,000 mmH 2 O.
- the moisture permeability is preferably not less than 6,000 g/m 2 ⁇ 24 h and the water pressure resistance is more preferably not lower than 6,000 mmH 2 O.
- the A-1 moisture permeability and the B-1 moisture permeability are less than 5,000 g/m 2 ⁇ 24 h, comfortable moisture permeating feel cannot be attained when the fabric is actually used, causing a stuffy feel.
- the water pressure resistance is lower than 5,000 mmH 2 O, practical waterproof property cannot be attained.
- the moisture permeabilities and the water pressure resistance are preferably greater.
- the above-described polyurethane resin is applied such that the thickness of the resulting resin film after drying becomes preferably 5 to 100 ⁇ m, more preferably 10 to 80 ⁇ m.
- the resin film thickness is less than 5 ⁇ m, practical waterproof property tends not to be attained, while when the resin film is thicker than 100 ⁇ m, practical moisture permeability tends not to be attained.
- the moisture-permeable waterproof fabric according to the present invention has excellent toughness; therefore, it is suitable as a fabricing material, particularly as a material for sporting wear and outdoor fabricing.
- the resin film formed on the moisture-permeable waterproof fabric of the present invention is a porous film.
- resin film is non-porous, a resin film exhibiting sufficient moisture permeability cannot be obtained.
- the fabric used in the present invention is not particularly restricted; however, examples thereof include fabrics made of polyamide fiber, polyester fiber and/or the like. Further, the mode of the fabric is also not particularly restricted and, for example, a woven fabric or a knitted fabric may be employed as appropriate.
- the moisture-permeable waterproof fabric according to the present invention can be produced by a method in which a polyurethane resin solution containing the above-described polyurethane resin as a major component is coated on at least one side of a fabric by a coating method.
- a coating method examples include those in which a fabric is directly coated using a knife coater, comma coater, roll coater, die coater, lip coater or the like.
- the moisture-permeable waterproof fabric according to the present invention can also be produced by a lamination method in which separately formed resin films are laminated on a fabric.
- lamination methods include a method in which, after coating the above-described polyurethane resin solution on a mold-releasing substrate, resin films obtained by immersion and coagulation in water or the like are laminated on one side of a fabric via an adhesive or the like.
- mold-releasing substrate is not particularly restricted and examples thereof include films made of a resin itself having releasing property for polyurethane resin (such as an olefin resin or silicon resin: hereinafter, referred to as “mold-releasing agent”); mold-releasing papers in which a mold-releasing layer composed of a mold-releasing agent is laminated on a substrate such as a paper, fabric or film; mold-releasing fabrics; and mold-releasing films.
- a resin itself having releasing property for polyurethane resin such as an olefin resin or silicon resin: hereinafter, referred to as “mold-releasing agent”
- mold-releasing papers in which a mold-releasing layer composed of a mold-releasing agent is laminated on a substrate such as a paper, fabric or film
- mold-releasing fabrics mold-releasing fabrics
- mold-releasing films Preferred thereamong from the standpoint of the mold-releasing property are olefin resin films and mold-releasing films in which a mold-releasing layer composed of an olefin resin is laminated on
- the mold-releasing substrate may have an irregular configuration as well and by using such a mold-releasing substrate, a resin film having an irregularly configured surface can be formed, so that not only blocking between film surfaces can be prevented, but also a moisture-permeable waterproof fabric with a pleasant texture can be obtained.
- the conditions of coating film formation may be, for example, those of a wet coagulation system; however, they are not particularly restricted. Specific examples of the conditions include those of a method in which a polyurethane resin solution prepared by dissolving the above-described polyurethane resin in a water-soluble polar solvent such as DMF is coated on a fabric and coagulated in water or an aqueous solution containing a polar solvent to form a porous film.
- the resulting polyurethane resins and moisture-permeable waterproof fabrics were subjected to the following performance evaluations.
- test sample A resin solution adjusted to have a polyurethane resin concentration of 15% was applied to a mold-releasing paper to a thickness of 150 ⁇ m and the resultant was dried for 3 minutes using an air-circulating dryer at 120° C. and then allowed to cool. The resulting coating film was removed from the mold-releasing paper to obtain a coating film of 20 ⁇ m in thickness.
- Tensile strength measurement method In accordance with JIS L 1096, a test piece of 25 mm in width was stretched at a grip distance of 50 mm and a tensile rate of 150 mm/min to measure the stress value, breaking strength and elongation at break when the test piece was stretched at 100%.
- JIS L 1096 JIS L 1096
- a test piece of 25 mm in width was stretched at a grip distance of 50 mm and a tensile rate of 150 mm/min to measure the stress value, breaking strength and elongation at break when the test piece was stretched at 100%.
- an autograph AG-IS manufactured by Shimadzu Corporation was employed.
- the polyurethane resins used in Examples 1 and 2 which were produced by using a 100% plant-based sebacic acid-based polyol as a starting material, exhibited equivalent or superior toughness (stress value, breaking strength and elongation at break when stretched at 100%) as compared to the polyurethane resin of Comparative Example 3 produced by using a petroleum-based material and the moisture permeability and waterproof property of the resulting fabrics were also comparable and good.
- a plant-based percentage was attained at a certain level or greater and the fabrics exhibited good moisture permeability, waterproof property and toughness; therefore, a moisture-permeable waterproof fabric intended in the present invention was obtained.
- Comparative Example 1 since the polyol/isocyanate equivalent ratio of the polyurethane resin was large at 1/1.2, a porous film intended in the present invention was not obtained and the resulting fabric had low moisture permeability and a low water-resistance property. It is noted here that the obtained polyurethane resin coating film was in the form of an adhesive, so that the tensile strength thereof could not be measured.
- the polyurethane resin of Comparative Example 2 had a small polyol/isocyanate equivalent ratio of 1/60; therefore, it was difficult to control the reaction and a resin solution suitable for coating could not be obtained.
- Comparative Example 4 since a polyol produced from recinoleic acid which is generally commercially available as a castor oil-based polyol was used, the toughness was comparable; however, the moisture permeability and waterproof performance intended in the present invention could not be attained despite that the polyurethane resin film was porous.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Polyurethanes Or Polyureas (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Disclosed is a moisture-permeable waterproof fabric which is produced by using a plant-based material and has equivalent or superior performance as compared to conventional petroleum-based polyurethane resins. The moisture-permeable waterproof fabric comprises, on at least one surface thereof, a porous resin film composed of a polyurethane resin containing 5 to 80% by weight of a sebacic acid-based polyol component produced from a plant-based sebacic acid, and has an A-1 moisture permeability and a B-1 moisture permeably both of which are not less than 5,000 g/m2·24 h and a water pressure resistance of not lower than 5,000 mmH2O.
Description
- The present invention relates to a moisture-permeable waterproof fabric, particularly a moisture-permeable waterproof fabric which comprises a plant-based component and has equivalent or superior performance as compared to conventional petroleum-based polyurethane resins.
- Conventionally, as a material used in a moisture-permeable waterproof fabric, polyurethane resins are widely employed for their excellent mechanical characteristics, and porous films of polyurethane resins prepared by a wet coagulation system and non-porous films of polyurethane resins having a hydrophilic group are utilized.
- Further, in recent years, from the standpoint of reducing environmental load, moisture-permeable waterproof fabrics in which a resin comprising a plant-based component is used have been developed and as such a resin, polylactic resins are widely known. For example, Unexamined Japanese Patent Application Kokai Publication No. 2002-20530 discloses a wet-type porous film structure in which a polylactic resin is used as a plant-based component.
- However, the water pressure resistance (JIS L 1092 A method) of the wet-type porous film structure disclosed in the above-described Patent Literature is about 1,600 mmH2O and the water resistance is thus not sufficient from the standpoint of practical waterproofing.
- In addition, polylactic resins generally lack toughness, so that they become fragile and lack flexibility especially when they are made into a porous film. Thus, it is difficult to use a polylactic resin in apparel applications and the like.
- Further, it is known to utilize a polyol such as a castor oil or a modified castor oil, which is a plant-based component, as a starting material of a polyurethane resin. For example, Unexamined Japanese Patent Application Kokai Publication No. 2009-149876 discloses a moisture-permeable polyurethane resin comprising a plant-based polymeric diol component produced from castor oil. Here, by using this plant-based polymeric diol component in combination with a polymeric diol component containing an oxyethylene group which is a hydrophilic group, the resulting polyurethane resin is imparted with hydrophilicity in order to improve the moisture permeability. However, the hydrophilic polyurethane resin is not porous, so that there is a problem in that it is difficult to attain sufficient moisture permeability (JIS L-1099 A-1 method).
- Further, castor oil is a composition mainly composed of fatty acid triglyceride and the principal component of the constituent fatty acid is ricinoleic acid; therefore, castor oil has about 2.7 hydroxyl groups per molecule. Yet, when a polyol having more than 2 hydroxyl groups per molecule is used, since a branched structure or a cross-linked structure is formed, the resulting polyurethane resin becomes overly hardened, so that a resin film satisfying practically appropriate flexibility (texture) cannot be obtained. Moreover, when the viscosity becomes excessively high due to an increase in the formation of branched structure or cross-linked structure, there arises a problem that a resin or a resin solution suitable for coating or the like in the formation of a resin film cannot be obtained.
- Further, as other plant-based polyol used as a starting material of a polyurethane resin, dicarboxylic acid-based diols such as sebacic acid are known. As a polyurethane resin produced by using a dicarboxylic acid-based diol, for example, Unexamined Japanese Patent Application Kokai Publication No. H07-88833 discloses a moisture-permeable porous sheet material prepared by a wet coagulation system and JP 4329046B discloses a moisture curable-type hot melt film. However, the former does not have a practically sufficient level of moisture permeability and waterproof property; therefore, it has a problem of being not suitable as an outdoor sporting wear material where high moisture permeability and water-resistance are required. Further, the latter is not suitable for mass production because of the complicated production process thereof and also has a problem in that, since the polyurethane resin has hydrophilic groups, the film has high water-swellability, which potentially causes a marked decrease in the strength upon contact with water or the like. Moreover, expression of moisture permeability, waterproof property, mechanical strength and the like in a polyurethane resin by these techniques is largely dependent on the components and additives constituting the polyurethane resin other than sebacic acid; therefore, there is a limitation in terms of designable structure.
- That is, with respect to moisture-permeable waterproof fabrics utilizing a porous film, those having a porous resin film composed of a petroleum-based component are still the mainstream and at present, no practical moisture-permeable waterproof fabric having a porous film composed of a plant-based component is available on the market.
- An object of the present invention is to solve the above-described problems, in particular, to provide a moisture-permeable waterproof fabric which comprises a plant-based component contributing to a reduction in environmental load and exhibits equivalent or superior performance as compared to a case where a conventional petroleum-based polyurethane resin is used.
- The present inventors intensively studied to discover that the above-described problems can be solved by using, as a starting material of a polyurethane resin, a sebacic acid-based polyol-component which is produced from sebacic acid obtained from castor oil or the like as a plant-based component, thereby completing the present invention.
- That is, the present invention relates to a moisture-permeable waterproof fabric which comprises, on at least one surface thereof, a porous resin film composed of a polyurethane resin containing 5 to 80% by weight of a sebacic acid-based polyol component produced from a plant-based sebacic acid, wherein the moisture permeability measured by the JIS L1099 A-1 method and the moisture permeability measured by the JIS L1099 B-1 method are both not less than 5,000 g/m2·24 h and the water pressure resistance measured by the JIS L-1092 B method (high water pressure method) is not lower than 5,000 mmH2O.
- The above-described polyurethane resin is produced from at least a polyol component, an isocyanate component and a chain extender component and the molar ratio of the polyol component and the isocyanate component, polyol/isocyanate, is preferably between 1/6 and 1/2.
- The above-described sebacic acid-based polyol-component is preferably an α,ω-diol which is produced by a reaction of a plant-based sebacic acid and a diol and has a number average molecular weight of 500 to 5,000.
- According to the present invention, by mainly using a plant-based sebacic acid-based polyol component as a polyol component of a polyurethane resin, the toughness, which is a problem of using a plant-based resin such as polylactic acid resin, can be improved and an equivalent toughness as that of a polyurethane resin comprising a petroleum-based component can be attained. Further, a moisture permeability and waterproof performance equivalent or superior to a moisture-permeable waterproof fabric produced from a polyurethane resin comprising an existing petroleum-based component can be provided. Moreover, because of the use of a plant-based component, the moisture-permeable waterproof fabric of the present invention can contribute to a reduction in environmental load.
- The moisture-permeable waterproof fabric according to the present invention is characterized in that it comprises, on at least one surface thereof, a porous resin film composed of a polyurethane resin containing 5 to 80% by weight of a sebacic acid-based polyol component produced from a plant-based sebacic acid and that the moisture permeability measured by the JIS L1099 A-1 method and the moisture permeability measured by the JIS L1099 B-1 method are both not less than 5,000 g/m2·24 h and the water pressure resistance measured by the JIS L-1092 B method (high water pressure method) is not lower than 5,000 mmH2O.
- The sebacic acid used in the present invention is, for example, a C10 linear saturated dibasic acid obtained by a cleavage reaction of a vegetable oil such as castor oil by a caustic alkali. Generally, those commercially available castor oil-based polyols are produced from ricinoleic acid obtained by saponification decomposition of castor oil and are, therefore, different from those polyols produced from sebacic acid. Here, the material oil of the plant-based sebacic acid is not particularly restricted to castor oil.
- Castor oil is a compound mainly having the structure represented by the following formula 1.
-
- Further, sebacic acid is a dicarboxylic acid having the structure represented by the following formula 2.
-
HOOC(CH2)8COOH [formula 2] - Sebacic acid-based polyols are, as an alternative to polyester polyols and the like, used as a starting material of urethane used as an adhesive or a paint; however, in the present invention, it was discovered that a polyurethane resin produced by using sebacic acid as a starting material has high permeability and waterproof property as well as excellent toughness and such polyurethane resin was used as a principal material of a resin film of a moisture-permeable waterproof fabric.
- The sebacic acid-based polyol used in the present invention is preferably a sebacic acid-based polyester diol obtained by a reaction of a plant-based sebacic acid and a diol. Further, the upper limit of the number of carbon atoms in the diol is not particularly restricted; however, the number average molecular weight of the resulting sebacic acid-based polyol is in the range of preferably 500 to 5,000, more preferably 1,000 to 3,000. When the number average molecular weight is smaller than 500, the resulting polyurethane resin tends to be too hard, while when it is greater than 5,000, the resulting polyurethane resin tends to be too soft.
- Examples of the diol to be reacted with sebacic acid include diols such as ethylene glycol, propanediol, hexanediol, nonanediol, neopentyl glycol and polyethylene glycol (PEG). These diols may be used individually, or two or more thereof may be used in combination as required.
- Thereamong, from the standpoint of environmental load, it is preferred that a plant-based component be used also in the diol per se to be reacted with sebacic acid. In cases where the sebacic acid-based polyol is produced from a plant-based sebacic acid and a plant-based diol, the plant-based percentage of the polyol component is 100%. In this manner, when the plant-based percentage is calculated with consideration of the constituents of the sebacic acid-based polyol, the amount of the plant-based component(s) contained in the polyurethane resin is preferably 5 to 80% by weight, more preferably 6 to 75% by weight. When the amount of the plant-based component(s) is less than 5% by weight, the environmental load-reducing effect tends to be small, while when the amount is greater than 80% by weight, a polyurethane resin having sufficiently satisfactory moisture permeability, waterproof property, mechanical strength and the like may not be obtained and it may become difficult to obtain a porous resin film.
- In the polyurethane resin used in the present invention, the content of the sebacic acid-based polyol component obtained from a plant-based sebacic acid in a polyurethane-forming material is 5 to 80% by weight, preferably 6 to 75% by weight. The percentage of the above-described polyol component is preferably greater from the standpoint of environmental load; however, when it is greater than 80% by weight, it may become difficult to form a film or obtain a porous resin film, so that a polyurethane resin having sufficiently satisfactory moisture permeability, waterproof property, mechanical strength and the like may not be obtained. Further, when the amount of the above-described polyol component is less than 5% by weight, the plant-based percentage of the resulting polyurethane resin is reduced; therefore, such an amount is not preferred from the standpoint of reducing environmental load.
- Further, as a polyol composed of an aliphatic dicarboxylic acid, which is normally used in the production of polyurethane, a polyol composed of a C4 to C12 dicarboxylic acid is commonly employed; however, since sebacic acid contains a greater number of carbon atoms as compared to adipic acid and the like commonly used as a starting material of a polyurethane resin, a polyurethane resin produced from a sebacic acid-based polyol can be expected to have an improved waterproof property. Thereamong, a polyurethane resin produced from the above-described polyol can be expected to have a good balance of the hydrophobicity and the mechanical strength, as well as an improved moisture permeability because of the porous film-forming property. When the amount of the above-described polyol component is less than 5% by weight, these effects may not be sufficiently attained; therefore, such an amount is not preferred.
- It is noted here that the “composition percentage of the sebacic acid-based polyol component” used herein relates to the percentage of all sebacic acid-based polyols produced from a plant-based sebacic acid, irrespective of the type thereof.
- As the polyol component of polyurethane resin used in the present invention, one produced from a dicarboxylic acid other than sebacic acid may also be used in combination. Examples of the dicarboxylic acid other than sebacic acid include dicarboxylic acids such as adipic acid, succinic acid, terephthalic acid and isophthalic acid that are derived from petroleum. The amount of these carboxylic acids to be used is preferably small in order not to reduce the plant-based percentage; however, it is set as appropriate with consideration of the above-described composition percentage and the later-described molar ratio of the polyol component and the isocyanate component.
- Further, as required, in addition to the above-described plant-based polyol, other dihydric polyol may also be used in combination. Specific examples thereof include petroleum-based dihydric polyols such as polyester polyols, polyether polyols, polycarbonate polyols, polyamide-based polyols, silicone-based polyols and fluorine-based polyols. In order not to reduce the plant-based percentage, these dihydric polyols are preferably added in the smallest amount possible.
- In cases where the above-described polyurethane resin is composed of a polyol component, an isocyanate component and a chain extender component, the molar ratio of the polyol component and the isocyanate component, polyol/isocyanate, is preferably between 1/6 and 1/2, more preferably between 1/5.5 and 1/2.5. When the amount of the isocyanate component is excessive, it tends to be difficult to control the reaction, while when the amount of the polyol component is excessive, it tends to be difficult to obtain a porous resin film.
- Here, the NCO/OH equivalent ratio of the isocyanate component, polyol component and chain extender component is usually 0.95 to 1.15, preferably substantially 1. When the NCO/OH equivalent ratio is not in this range, a polyurethane resin having a high molecular weight cannot be obtained, so that it tends to be difficult to produce a moisture-permeable waterproof fabric having useful performance.
- The number average molecular weight of the polyurethane resin used in the present invention is preferably between 50,000 and 500,000. When the number average molecular weight of the above-described polyurethane resin is not in the above-described range, a resin or resin solution suitable for coating and the like in the formation of a resin film cannot be obtained and it tends to be difficult to obtain a resin film which exhibits practical moisture permeability and water-resistance.
- As a method for obtaining a polyurethane resin, a conventional prepolymer method can be employed. Specifically, a method in which a prepolymer is prepared by allowing the above-described polyol and isocyanate to react in a solvent inert to isocyanate group, for example, a polar organic solvent such as dimethylformamide (DMF) or dimethyl sulfoxide (DMSO) or a non-polar organic solvent such as methyl ethyl ketone (MEK), toluene or xylene, and then the thus obtained prepolymer is allowed to react with a chain extender such as a diol to increase the degree of polymerization can be employed. It is noted here, however, that the production method of the polyurethane resin used in the present invention is not restricted to this method.
- The isocyanate component used in the present invention is not particularly restricted; however, examples thereof include diisocyanates represented by aromatic diisocyanates such as xylene diisocyanate, 4,4′-diphenylmethane diisocyanate (MDI) and 2,4- and/or 2,6-tolylene diisocyanate; aliphatic diisocyanates such as hexamethylene diisocyanate and lysine diisocyanate; and alicyclic diisocyanates such as tetramethylene diisocyanate, isophorone diisocyanate and hydrogenated MDI. These isocyanates may be used individually, or two or more thereof may be used in combination as required.
- Further, the chain extender component is not particularly restricted; however, generally, a diol having a relatively low molecular weight is employed. Examples of such diol include ethylene glycol, diethylene glycol, propanediol, butanediol, hexanediol and polyethylene glycol (PEG) that are derived from petroleum; and 1,3-propanediol and 1,2-hexanediol that are derived from a plant. These diols may be used individually, or two or more thereof may be used in combination as required. In addition, a diamine and/or the like may also be used as required. The chain extender is generally used primarily for controlling the molecular weight and physical properties of the resulting film in the synthesis of a resin used as a moisture-permeable waterproof film.
- The above-described polyurethane resin may be used by diluting it with an organic solvent or the like as required. Further, to the above-described polyurethane resin, an antioxidant, a stabilizer such as a light resistance-improving agent, an inorganic filler, a non-solvent, a lubricant, a water repellant, a pigment, other additive(s) and/or a function-imparting agent may also be added as appropriate.
- The moisture-permeable waterproof fabric according to the present invention comprises the above-described polyurethane resin on at least one surface thereof and within the moisture-permeable waterproof fabric, the moisture permeability measured by the JIS L1099 A-1 method and the moisture permeability measured by the JIS L1099 B-1 method are both not less than 5,000 g/m2·24 h and the water pressure resistance measured by the JIS L1092 B method (high water pressure method) is not lower than 5,000 mmH2O. The moisture permeability is preferably not less than 6,000 g/m2·24 h and the water pressure resistance is more preferably not lower than 6,000 mmH2O. When the A-1 moisture permeability and the B-1 moisture permeability are less than 5,000 g/m2·24 h, comfortable moisture permeating feel cannot be attained when the fabric is actually used, causing a stuffy feel. In cases where the water pressure resistance is lower than 5,000 mmH2O, practical waterproof property cannot be attained. The moisture permeabilities and the water pressure resistance are preferably greater.
- The above-described polyurethane resin is applied such that the thickness of the resulting resin film after drying becomes preferably 5 to 100 μm, more preferably 10 to 80 μm. When the resin film thickness is less than 5 μm, practical waterproof property tends not to be attained, while when the resin film is thicker than 100 μm, practical moisture permeability tends not to be attained.
- The moisture-permeable waterproof fabric according to the present invention has excellent toughness; therefore, it is suitable as a fabricing material, particularly as a material for sporting wear and outdoor fabricing.
- Further, the resin film formed on the moisture-permeable waterproof fabric of the present invention is a porous film. When resin film is non-porous, a resin film exhibiting sufficient moisture permeability cannot be obtained.
- The fabric used in the present invention is not particularly restricted; however, examples thereof include fabrics made of polyamide fiber, polyester fiber and/or the like. Further, the mode of the fabric is also not particularly restricted and, for example, a woven fabric or a knitted fabric may be employed as appropriate.
- The moisture-permeable waterproof fabric according to the present invention can be produced by a method in which a polyurethane resin solution containing the above-described polyurethane resin as a major component is coated on at least one side of a fabric by a coating method. Examples of the method include those in which a fabric is directly coated using a knife coater, comma coater, roll coater, die coater, lip coater or the like.
- Further, the moisture-permeable waterproof fabric according to the present invention can also be produced by a lamination method in which separately formed resin films are laminated on a fabric. Examples of such lamination methods include a method in which, after coating the above-described polyurethane resin solution on a mold-releasing substrate, resin films obtained by immersion and coagulation in water or the like are laminated on one side of a fabric via an adhesive or the like.
- The above-described mold-releasing substrate is not particularly restricted and examples thereof include films made of a resin itself having releasing property for polyurethane resin (such as an olefin resin or silicon resin: hereinafter, referred to as “mold-releasing agent”); mold-releasing papers in which a mold-releasing layer composed of a mold-releasing agent is laminated on a substrate such as a paper, fabric or film; mold-releasing fabrics; and mold-releasing films. Preferred thereamong from the standpoint of the mold-releasing property are olefin resin films and mold-releasing films in which a mold-releasing layer composed of an olefin resin is laminated on a polyester resin film. The mold-releasing substrate may have an irregular configuration as well and by using such a mold-releasing substrate, a resin film having an irregularly configured surface can be formed, so that not only blocking between film surfaces can be prevented, but also a moisture-permeable waterproof fabric with a pleasant texture can be obtained.
- The conditions of coating film formation may be, for example, those of a wet coagulation system; however, they are not particularly restricted. Specific examples of the conditions include those of a method in which a polyurethane resin solution prepared by dissolving the above-described polyurethane resin in a water-soluble polar solvent such as DMF is coated on a fabric and coagulated in water or an aqueous solution containing a polar solvent to form a porous film.
- The present invention will now be described more concretely by way of examples thereof; however, the present invention is not restricted to the following examples. In the following examples, unless otherwise specified, “%” and “part” are by weight.
- The resulting polyurethane resins and moisture-permeable waterproof fabrics were subjected to the following performance evaluations.
- Preparation of test sample: A resin solution adjusted to have a polyurethane resin concentration of 15% was applied to a mold-releasing paper to a thickness of 150 μm and the resultant was dried for 3 minutes using an air-circulating dryer at 120° C. and then allowed to cool. The resulting coating film was removed from the mold-releasing paper to obtain a coating film of 20 μm in thickness.
- Tensile strength measurement method: In accordance with JIS L 1096, a test piece of 25 mm in width was stretched at a grip distance of 50 mm and a tensile rate of 150 mm/min to measure the stress value, breaking strength and elongation at break when the test piece was stretched at 100%. For the measurement, an autograph AG-IS manufactured by Shimadzu Corporation was employed.
- In accordance with the JIS L-1099 A-1 and B-1 methods, the moisture permeability of moisture-permeable waterproof fabric was measured.
- In accordance with the JIS L-1092 B method (high water pressure method), the water pressure resistance of moisture-permeable waterproof fabric was measured.
- Under a dry nitrogen atmosphere, 50 g of a plant-based sebacic acid-based polyol 1 (HS2P-103S manufactured by HOKOKU Co., Ltd.; number average molecular weight: 1,000, components: sebacic acid/propanediol, plant-based percentage: 100%) was dissolved in 393 g of DMF. To the thus obtained solution, 63 g of MDI (polyol/isocyanate molar ratio: 1/5) was added, and the resultant was allowed to react at 70° C. for 2 hours to obtain a prepolymer. Then, 18 g of 1,4-butanediol was added and allowed to react at 60° C. for 3 hours to obtain a polyurethane resin 25% solution 1 (number average molecular weight: 135,200) containing 38% of a sebacic acid-based polyol component (solid content percentage).
- Thereafter, 100 parts of the thus obtained plant-based polyurethane resin 25% solution 1, 20 parts of DMF, 6 parts of a hydrophobic silica (NIPSIL SS-50 manufactured by Tosoh Silica Corporation) and 1 part of a curing agent (CORONATE HX manufactured by Nippon Polyurethane Industry Co., Ltd.) were mixed with stirring to obtain a polyurethane resin mixture.
- Then, to nylon taffeta subjected to a water-repellent treatment in advance, the thus obtained polyurethane resin mixture was applied using a roll-on knife coater to a thickness after drying of 40 μm and coagulated in water for 2 minutes. Further, the resultant was washed by immersion in warm water at 50° C. for 3 minutes and dried at 150° C. for 1 minute to obtain a moisture-permeable waterproof fabric having a polyurethane resin film. The evaluation results are shown in Table 1.
- Under a dry nitrogen atmosphere, 50 g of a plant-based sebacic acid-based polyol 2 (HS2P-203S manufactured by HOKOKU Co., Ltd.; number average molecular weight: 2,000, components: sebacic acid/propanediol, plant-based percentage: 100%) was dissolved in 270 g of DMF. To the thus obtained solution, 31 g of MDI (polyol/isocyanate equivalent ratio: 1/5) was added, and the resultant was allowed to react at 70° C. for 2 hours to obtain a prepolymer. Then, 9.0 g of 1,4-butanediol was added and allowed to react at 60° C. for 3 hours to obtain a polyurethane resin 25% solution 2 (number average molecular weight: 123,200) containing 56% of a sebacic acid-based polyol component (solid content percentage).
- Thereafter, 100 parts of the thus obtained plant-based polyurethane resin 25% solution 2, 20 parts of DMF, 6 parts of a hydrophobic silica (NIPSIL SS-50 manufactured by Tosoh Silica Corporation) and 1 part of a curing agent (CORONATE FIX manufactured by Nippon Polyurethane Industry Co., Ltd.) were mixed by stirring to obtain a polyurethane resin mixture.
- Then, to nylon taffeta subjected to a water-repellent treatment in advance, the thus obtained polyurethane resin mixture was applied using a roll-on knife coater to a thickness after drying of 40 μm and coagulated in water for 2 minutes. Further, the resultant was washed by immersion in warm water at 50° C. for 3 minutes and dried at 150° C. for 1 minute to obtain a moisture-permeable waterproof fabric having a polyurethane resin film. The evaluation results are shown in Table 1.
- Under a dry nitrogen atmosphere, 50 g of a plant-based sebacic acid-based polyol 3 (HS2H-2005 manufactured by HOKOKU Co., Ltd.; number average molecular weight: 2,000, components: sebacic acid/hexanediol, plant-based percentage: 60%) was dissolved in 220 g of DMF. To the thus obtained solution, 19 g of MDI (polyol/isocyanate equivalent ratio: 1/3) was added, and the resultant was allowed to react at 70° C. for 2 hours to obtain a prepolymer. Then, 4.5 g of 1,4-butanediol was added and allowed to react at 60° C. for 3 hours to obtain a polyurethane resin 25% solution 3 (number average molecular weight: 139,600) containing 68% of a sebacic acid-based polyol component (solid content percentage).
- Thereafter, 100 parts of the thus obtained plant-based polyurethane resin 25% solution 3, 20 parts of DMF, 6 parts of a hydrophobic silica (NIPSIL SS-50 manufactured by Tosoh Silica Corporation) and 1 part of a curing agent (CORONATE FIX manufactured by Nippon Polyurethane Industry Co., Ltd.) were mixed with stirring to obtain a polyurethane resin mixture.
- Then, to nylon taffeta subjected to a water-repellent treatment in advance, the thus obtained polyurethane resin mixture was applied using a roll-on knife coater to a thickness after drying of 40 μm and coagulated in water for 2 minutes. Further, the resultant was washed by immersion in warm water at 50° C. for 3 minutes and dried at 150° C. for 1 minute to obtain a moisture-permeable waterproof fabric having a polyurethane resin film. The evaluation results are shown in Table 1.
- Under a dry nitrogen atmosphere, 20 g of a plant-based sebacic acid-based polyol 1 (HS2P-1035 manufactured by HOKOKU Co., Ltd.; number average molecular weight: 1,000, components: sebacic acid/propanediol, plant-based percentage: 100%) and 60 g of an adipic acid-based polyol (P-2010 manufactured by KURARAY Co., Ltd.; number average molecular weight: 2,000) were dissolved in 482 g of DMF. To the thus obtained solution, 63 g of MDI (polyol/isocyanate equivalent ratio: 1/5) was added, and the resultant was allowed to react at 70° C. for 2 hours to obtain a prepolymer. Then, 18 g of 1,4-butanediol was added and allowed to react at 60° C. for 3 hours to obtain a polyurethane resin 25% solution 4 (number average molecular weight: 140,100) containing 12% of a sebacic acid-based polyol component (solid content percentage).
- Thereafter, 100 parts of the thus obtained plant-based polyurethane resin 25% solution 4, 20 parts of DMF, 6 parts of NIPSIL SS-50 (manufactured by Tosoh Silica Corporation) and 1 part of CORONATE HX (manufactured by Nippon Polyurethane Industry Co., Ltd.) were mixed with stirring to obtain a polyurethane resin mixture.
- Then, to nylon taffeta subjected to a water-repellent treatment in advance, the thus obtained polyurethane resin mixture was applied using a roll-on knife coater to a thickness after drying of 40 μm and coagulated in water for 2 minutes. Further, the resultant was washed by immersion in warm water at 50° C. for 3 minutes and dried at 150° C. for 1 minute to obtain a moisture-permeable waterproof fabric having a polyurethane resin film. The evaluation results are shown in Table 1.
- Under a dry nitrogen atmosphere, 50 g of a plant-based sebacic acid-based polyol 3 (HS2H-2005 manufactured by HOKOKU Co., Ltd.; number average molecular weight: 2,000, components: sebacic acid/hexanediol, plant-based percentage: 60%) was dissolved in 174 g of DMF. To the thus obtained solution, 7.5 g of MDI (polyol/isocyanate equivalent ratio: 1/1.2) was added, and the resultant was allowed to react at 70° C. for 2 hours to obtain a prepolymer. Then, 0.45 g of 1,4-butanediol was added and allowed to react at 60° C. for 3 hours to obtain a polyurethane resin 25% solution 5 (number average molecular weight: 60,400) containing 86% of a sebacic acid-based polyol component (solid content percentage).
- Thereafter, 100 parts of the thus obtained plant-based polyurethane resin 25% solution 5, 20 parts of DMF, 6 parts of a hydrophobic silica (NIPSIL SS-50 manufactured by Tosoh Silica Corporation) and 1 part of a curing agent (CORONATE FIX manufactured by Nippon Polyurethane Industry Co., Ltd.) were mixed by stirring to obtain a polyurethane resin mixture.
- Then, to a nylon taffeta subjected to a water-repellent treatment in advance, the thus obtained polyurethane resin mixture was applied using a roll-on knife coater to a thickness after drying of 40 μm and coagulated in water for 2 minutes. Further, the resultant was washed by immersion in warm water at 50° C. for 3 minutes and dried at 150° C. for 1 minute to obtain a moisture-permeable waterproof fabric having a polyurethane resin film. The evaluation results are shown in Table 1.
- Under a dry nitrogen atmosphere, 20 g of a plant-based sebacic acid-based polyol 1 (HS2P-103S manufactured by HOKOKU Co., Ltd.; number average molecular weight: 1,000, components: sebacic acid/propanediol, plant-based percentage: 100%) was dissolved in 1,280 g of DMF. To the thus obtained solution, 300 g of MDI (polyol/isocyanate equivalent ratio: 1/60) was added, and the resultant was allowed to react at 70° C. for 2 hours to obtain a prepolymer. Then, when 106 g of 1,4-butanediol was added, gelation of the resin solution occurred, so that a resin solution suitable for coating was not obtained (sebacic acid-based polyol component: 4.7% (solid content percentage)). The evaluation results are shown in Table 1.
- Under a dry nitrogen atmosphere, 50 g of an adipic acid-based polyol (P-2010 manufactured by KURARAY Co., Ltd.; number average molecular weight: 2,000) was dissolved in 270 g of DMF. To the thus obtained solution, 31 g of MDI (polyol/isocyanate equivalent ratio: 1/5) was added, and the resultant was allowed to react at 70° C. for 2 hours to obtain a prepolymer. Then, 9.0 g of 1,4-butanediol was added and allowed to react at 60° C. for 3 hours to obtain a polyurethane resin 25% solution (number average molecular weight: 130,700,) containing no sebacic acid-based polyol component (petroleum-based percentage: 100%).
- Thereafter, 100 parts of the thus obtained petroleum-based polyurethane resin 25% solution, 20 parts of DMF, 6 parts of a hydrophobic silica (NIPSIL SS-50 manufactured by Tosoh Silica Corporation) and 1 part of a curing agent (CORONATE FIX manufactured by Nippon Polyurethane Industry Co., Ltd.) were mixed by stirring to obtain a polyurethane resin mixture.
- Then, to nylon taffeta subjected to a water-repellent treatment in advance, the thus obtained polyurethane resin mixture was applied using a roll-on knife coater to a thickness after drying of 40 μm and coagulated in water for 2 minutes. Further, the resultant was washed by immersion in warm water at 50° C. for 3 minutes and dried at 150° C. for 1 minute to obtain a moisture-permeable waterproof fabric having a polyurethane resin film. The evaluation results are shown in Table 1.
- Under a dry nitrogen atmosphere, 50 g of a castor oil-based polyol (PH-5001 manufactured by Itoh Oil Chemicals Co., Ltd.; number average molecular weight: 2,500) was dissolved in 247 g of DMF. To the thus obtained solution, 25 g of MDI (polyol/isocyanate equivalent percentage: 1/5) was added, and the resultant was allowed to react at 70° C. for 2 hours to obtain a prepolymer. Then, 7.2 g of 1,4-butanediol was added and allowed to react at 60° C. for 3 hours to obtain a polyurethane resin 25% solution 6 (number average molecular weight: 141,000) containing 61% of a castor oil-based polyol component (solid content percentage).
- Thereafter, 100 parts of the thus obtained plant-based polyurethane resin 25% solution 6, 20 parts of DMF, 6 parts of a hydrophobic silica (NIPSIL SS-50 manufactured by Tosoh Silica Corporation) and 1 part of a curing agent (CORONATE HX manufactured by Nippon Polyurethane Industry Co., Ltd.) were mixed by stirring to obtain a polyurethane resin mixture.
- Then, to a nylon taffeta subjected to a water-repellent treatment in advance, the thus obtained polyurethane resin mixture was applied using a roll-on knife coater to a thickness after drying of 40 μm and coagulated in water for 2 minutes. Further, the resultant was washed by immersion in warm water at 50° C. for 3 minutes and dried at 150° C. for 1 minute to obtain a moisture-permeable waterproof fabric having a polyurethane resin film. The evaluation results are shown in Table 1.
-
TABLE 1 Comparative Comparative Comparative Comparative Example 1 Example 2 Example 3 Example 4 Example 1 Example 2 Example 3 Example 4 Polyurethane Polyol/isocyanate 1/5 1/5 1/3 1/5 1/1.2 1/60 1/5 1/5 resin equivalent ratio Content of plant based 38 56 68 12 86 4.7 0.0 0.0 sebacic acid based polyol (%) 100% stress of coating film 14.5 6.45 7.20 8.51 — — 5.86 4.38 (MPa) Breaking strength of 28.5 20.5 30.0 27.8 — — 27.3 22.9 coating film (MPa) Elongation at break of 250 364 310 264 — — 280 304.6 coating film (%) Resin film of Content of plant based 30 44 53 9.7 67 — 0.0 0.0 moisture- sebacic acid based polyol permeable (%) waterproof 1 moisture permeability 10,200 7,500 10,500 8,100 2,900 — 7,700 4,300 fabric (g/m2 · 24 h) 1 moisture permeability 10,400 7,100 12,800 6,600 2,400 — 6,500 3,700 (g/m2 · 24 h) (mm H2O) 11,000 7,500 11,700 7,700 3,800 — 7,000 4,500 Cross sectional structure porous porous porous porous non porous — porous porous of resin film - The polyurethane resins used in Examples 1 and 2, which were produced by using a 100% plant-based sebacic acid-based polyol as a starting material, exhibited equivalent or superior toughness (stress value, breaking strength and elongation at break when stretched at 100%) as compared to the polyurethane resin of Comparative Example 3 produced by using a petroleum-based material and the moisture permeability and waterproof property of the resulting fabrics were also comparable and good. In Examples 3 and 4 as well, a plant-based percentage was attained at a certain level or greater and the fabrics exhibited good moisture permeability, waterproof property and toughness; therefore, a moisture-permeable waterproof fabric intended in the present invention was obtained.
- On the other hand, in Comparative Example 1, since the polyol/isocyanate equivalent ratio of the polyurethane resin was large at 1/1.2, a porous film intended in the present invention was not obtained and the resulting fabric had low moisture permeability and a low water-resistance property. It is noted here that the obtained polyurethane resin coating film was in the form of an adhesive, so that the tensile strength thereof could not be measured.
- Further, the polyurethane resin of Comparative Example 2 had a small polyol/isocyanate equivalent ratio of 1/60; therefore, it was difficult to control the reaction and a resin solution suitable for coating could not be obtained.
- In Comparative Example 4, since a polyol produced from recinoleic acid which is generally commercially available as a castor oil-based polyol was used, the toughness was comparable; however, the moisture permeability and waterproof performance intended in the present invention could not be attained despite that the polyurethane resin film was porous.
Claims (3)
1. A moisture-permeable waterproof fabric, characterized by comprising, on at least one surface thereof, a porous resin film composed of a polyurethane resin containing 5 to 80% by weight of a sebacic acid-based polyol component produced from a plant-based sebacic acid, wherein the moisture permeability measured by JIS L1099 A-1 method and the moisture permeability measured by JIS L1099 B-1 method are both not less than 5,000 g/m2·24 h and the water pressure resistance measured by JIS L-1092 B method (high water pressure method) is not lower than 5,000 mmH2O.
2. The moisture-permeable waterproof fabric according to claim 1 , wherein said polyurethane resin comprises at least a polyol component, an isocyanate component and a chain extender component and the molar ratio of said polyol component and said isocyanate component, polyol/isocyanate, is between 1/6 and 1/2.
3. The moisture-permeable waterproof fabric according to claim 1 or 2 , wherein said sebacic acid-based polyol component is an α,ω-diol which is produced by a reaction of sebacic acid and a diol and has a number average molecular weight of 500 to 5,000.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2010036875 | 2010-02-23 | ||
| JP2010-036875 | 2010-02-23 | ||
| PCT/JP2011/054427 WO2011105595A1 (en) | 2010-02-23 | 2011-02-22 | Moisture-permeable water-proofing cloth |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20120322328A1 true US20120322328A1 (en) | 2012-12-20 |
Family
ID=44506991
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US13/580,278 Abandoned US20120322328A1 (en) | 2010-02-23 | 2011-02-22 | Moisture-permeable waterproof fabric |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US20120322328A1 (en) |
| EP (1) | EP2540908B1 (en) |
| JP (1) | JP5680052B2 (en) |
| CN (1) | CN102762792B (en) |
| WO (1) | WO2011105595A1 (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20180352905A1 (en) * | 2017-06-13 | 2018-12-13 | Shuang Bang Industrial Corp | Moisture-Permeable Waterproof Shoe Having an Upper Made of Jacquard Woven Fabric |
| US11198790B2 (en) * | 2019-03-21 | 2021-12-14 | Ddp Specialty Electronic Materials Us, Llc | Water-resistive coating composition |
| CN114258442A (en) * | 2019-09-20 | 2022-03-29 | Dic株式会社 | Moisture-permeable waterproof fabric |
| US11752702B2 (en) | 2017-09-01 | 2023-09-12 | Basf Se | Method for welding membranes |
| CN117211085A (en) * | 2023-08-08 | 2023-12-12 | 宁波厚阳户外用品有限公司 | A kind of waterproof clothing fabric |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5604352B2 (en) * | 2010-04-02 | 2014-10-08 | 大日精化工業株式会社 | Bio polyurethane resin |
| JP2011241528A (en) * | 2010-04-20 | 2011-12-01 | Seiren Co Ltd | Synthetic leather |
| CN107163208B (en) * | 2017-06-01 | 2020-10-13 | 黑龙江泰纳科技集团股份有限公司 | Durable environment-friendly fluorine-containing nano three-proofing finishing agent and preparation method and application thereof |
| KR102778729B1 (en) * | 2019-06-25 | 2025-03-12 | 디아이씨 가부시끼가이샤 | Laminate |
| CN114206966A (en) * | 2019-09-06 | 2022-03-18 | Dic株式会社 | Urethane resin composition and moisture permeable film |
| CN114222772B (en) * | 2019-09-20 | 2023-12-08 | Dic株式会社 | Moisture-hardening polyurethane hot-melt resin composition, adhesive and laminate |
| WO2021132657A1 (en) * | 2019-12-26 | 2021-07-01 | 東レコーテックス株式会社 | Moisture-permeable waterproof fabric |
| JP7009675B1 (en) * | 2020-06-03 | 2022-01-25 | 明成化学工業株式会社 | Water repellent composition, kit, water repellent fiber product and its manufacturing method |
| WO2025089017A1 (en) * | 2023-10-26 | 2025-05-01 | セーレン株式会社 | Waterproof sound-permeable film and electric product |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5070173A (en) * | 1987-08-04 | 1991-12-03 | Asahi Kasei Kogyo Kabushiki Kaisha | Thermoplastic polyurethane |
| US5520998A (en) * | 1992-10-12 | 1996-05-28 | Toray Industries, Inc. | Highly water-pressure-resistant and highly moisture-permeable waterproof sheet and method for producing same |
| US20080210132A1 (en) * | 2005-04-22 | 2008-09-04 | Asahi Glass Co., Ltd. | Isocyanate group-terminated urethane prepolymer, process for producing the same, and adhesive comprising the urethane prepolymer |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE513366A (en) * | 1951-08-22 | |||
| US5869593A (en) * | 1991-07-01 | 1999-02-09 | H. B. Fuller Licensing & Financing, Inc. | High moisture vapor transmission hot melt moisture cure polyurethane adhesive |
| JPH0788833A (en) | 1993-09-21 | 1995-04-04 | Tokyu Constr Co Ltd | Method for kneading of mortar or concrete |
| JP3921854B2 (en) * | 1998-12-17 | 2007-05-30 | 東レ株式会社 | Moisture permeable waterproof material and method for producing the same |
| JP2002020530A (en) | 2000-07-05 | 2002-01-23 | Toyo Cloth Co Ltd | Biodegradable porous membrane, structural material and method for producing the same |
| US20090061172A1 (en) * | 2006-01-26 | 2009-03-05 | Komatsu Seiren Co., Ltd. | Polyurethane Resin Composition for Durable Moisture-Permeable Waterproof Sheet, Moisture-Permeable Waterproof Sheet and Method of Manufacturing the Same |
| CA2657566A1 (en) * | 2006-07-24 | 2008-01-31 | F. Hoffmann-La Roche Ag | Pyrazoles as glucokinase activators |
| JP2008291386A (en) * | 2007-05-24 | 2008-12-04 | Teijin Fibers Ltd | Moisture-permeating and waterproofing garment |
| JP5496496B2 (en) | 2007-11-30 | 2014-05-21 | 東レコーテックス株式会社 | Moisture permeable polyurethane resin composed of plant-derived components |
| JP2009161898A (en) * | 2007-12-12 | 2009-07-23 | Toray Coatex Co Ltd | Glove insert made of plant-originated component |
| US8277930B2 (en) | 2008-02-27 | 2012-10-02 | Dic Corporation | Moisture-permeable film, production method of same and laminate using same |
-
2011
- 2011-02-22 US US13/580,278 patent/US20120322328A1/en not_active Abandoned
- 2011-02-22 WO PCT/JP2011/054427 patent/WO2011105595A1/en not_active Ceased
- 2011-02-22 CN CN201180009718.1A patent/CN102762792B/en active Active
- 2011-02-22 JP JP2012501901A patent/JP5680052B2/en active Active
- 2011-02-22 EP EP11747550.9A patent/EP2540908B1/en active Active
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5070173A (en) * | 1987-08-04 | 1991-12-03 | Asahi Kasei Kogyo Kabushiki Kaisha | Thermoplastic polyurethane |
| US5520998A (en) * | 1992-10-12 | 1996-05-28 | Toray Industries, Inc. | Highly water-pressure-resistant and highly moisture-permeable waterproof sheet and method for producing same |
| US20080210132A1 (en) * | 2005-04-22 | 2008-09-04 | Asahi Glass Co., Ltd. | Isocyanate group-terminated urethane prepolymer, process for producing the same, and adhesive comprising the urethane prepolymer |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20180352905A1 (en) * | 2017-06-13 | 2018-12-13 | Shuang Bang Industrial Corp | Moisture-Permeable Waterproof Shoe Having an Upper Made of Jacquard Woven Fabric |
| US11752702B2 (en) | 2017-09-01 | 2023-09-12 | Basf Se | Method for welding membranes |
| US11198790B2 (en) * | 2019-03-21 | 2021-12-14 | Ddp Specialty Electronic Materials Us, Llc | Water-resistive coating composition |
| CN114258442A (en) * | 2019-09-20 | 2022-03-29 | Dic株式会社 | Moisture-permeable waterproof fabric |
| US20220341090A1 (en) * | 2019-09-20 | 2022-10-27 | Dic Corporation | Moisture-permeable waterproof fabric |
| CN117211085A (en) * | 2023-08-08 | 2023-12-12 | 宁波厚阳户外用品有限公司 | A kind of waterproof clothing fabric |
Also Published As
| Publication number | Publication date |
|---|---|
| JP5680052B2 (en) | 2015-03-04 |
| WO2011105595A1 (en) | 2011-09-01 |
| EP2540908B1 (en) | 2017-04-26 |
| CN102762792B (en) | 2014-06-25 |
| JPWO2011105595A1 (en) | 2013-06-20 |
| EP2540908A4 (en) | 2013-10-23 |
| CN102762792A (en) | 2012-10-31 |
| EP2540908A1 (en) | 2013-01-02 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP2540908B1 (en) | Moisture-permeable water-proof fabric | |
| FI108045B (en) | Use of a substance consisting of a polyurethane system and an organic solvent in the preparation of water vapor permeable coatings | |
| KR20040029973A (en) | Polyurethane-Polyurea Dispersions as Coating Agents | |
| EP2436724B1 (en) | Process for producing porous object, and porous object, layered product, and leather-like sheet each obtained thereby | |
| KR101369334B1 (en) | Wet type polyurethane resin composition and the manufacturing method | |
| RU2412215C2 (en) | Polyurethaneurea solutions | |
| KR20160067135A (en) | Porous body and polishing pad | |
| KR101322761B1 (en) | The manufacturing method of polyurethane coating resin composition | |
| JP5210522B2 (en) | Polyurethane resin composition for moisture permeable waterproof fabric and moisture permeable waterproof fabric | |
| JP6674244B2 (en) | Thermosensitive coagulable water-based polyurethane resin composition, method for producing leather-like material using the composition, and leather-like material produced by the method | |
| JP2011241528A (en) | Synthetic leather | |
| JP6691699B2 (en) | Method for manufacturing waterproof fabric | |
| CA2302612A1 (en) | Polyurethane solutions terminated with amino-functional heterocyclic stoppers | |
| KR20110053652A (en) | Solvent-free polyurethane adhesive composition excellent in moisture permeability and manufacturing method of polyurethane adhesive using the same | |
| KR101259193B1 (en) | Coating agent composition and use thereof | |
| KR20170007776A (en) | Digitally printable topcoat | |
| JP6726383B2 (en) | Waterproof fabric | |
| JP2009203592A (en) | Coating material for fabric | |
| JP2020059928A (en) | Resin film and fiber cloth and fiber product formed by laminating it | |
| KR102808361B1 (en) | Polyurethane chain extender, composition for forming polyurethane resin, polyurethane resin, polyurethane resin composition, molded body and article | |
| KR102805571B1 (en) | Producing method of polyurethane resin for textile coating with excellent water-resistance and water-proofing, and textile coating fabric used it | |
| WO2026042801A1 (en) | Crosslinked polyurethane-urea resin and synthetic leather in which same is used | |
| KR20260032478A (en) | polyurethane resin composition | |
| JP2012051973A (en) | Polyurethane resin composition for synthetic leather, and synthetic leather using the same | |
| Szycher | Polyurethane coatings |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AS | Assignment |
Owner name: SEIREN CO., LTD., JAPAN Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:YAMADA, YOSHIYUKI;SAKAMOTO, KATSUMI;KATO, YOSHIHARU;REEL/FRAME:028821/0565 Effective date: 20120810 |
|
| STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |