JP2845517B2 - Breathable waterproof fabric - Google Patents
Breathable waterproof fabricInfo
- Publication number
- JP2845517B2 JP2845517B2 JP26812789A JP26812789A JP2845517B2 JP 2845517 B2 JP2845517 B2 JP 2845517B2 JP 26812789 A JP26812789 A JP 26812789A JP 26812789 A JP26812789 A JP 26812789A JP 2845517 B2 JP2845517 B2 JP 2845517B2
- Authority
- JP
- Japan
- Prior art keywords
- chitin
- fabric
- synthetic resin
- layer
- resin
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000004744 fabric Substances 0.000 title claims description 124
- 229920002101 Chitin Polymers 0.000 claims description 73
- 229920003002 synthetic resin Polymers 0.000 claims description 56
- 239000000057 synthetic resin Substances 0.000 claims description 56
- 239000000126 substance Substances 0.000 claims description 51
- 230000035699 permeability Effects 0.000 claims description 21
- 239000010410 layer Substances 0.000 description 91
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 53
- 229920005989 resin Polymers 0.000 description 37
- 239000011347 resin Substances 0.000 description 37
- 238000000034 method Methods 0.000 description 26
- 239000000463 material Substances 0.000 description 21
- 238000010521 absorption reaction Methods 0.000 description 19
- 239000007788 liquid Substances 0.000 description 18
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 17
- 238000000576 coating method Methods 0.000 description 15
- 239000005871 repellent Substances 0.000 description 15
- 239000011248 coating agent Substances 0.000 description 14
- 210000004243 sweat Anatomy 0.000 description 14
- 239000000243 solution Substances 0.000 description 13
- 230000000052 comparative effect Effects 0.000 description 12
- 229920001661 Chitosan Polymers 0.000 description 11
- 230000002940 repellent Effects 0.000 description 11
- 238000012360 testing method Methods 0.000 description 11
- -1 that is Polymers 0.000 description 11
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 9
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- 239000007864 aqueous solution Substances 0.000 description 9
- 239000000835 fiber Substances 0.000 description 9
- 238000010438 heat treatment Methods 0.000 description 9
- 238000011282 treatment Methods 0.000 description 9
- 229920000742 Cotton Polymers 0.000 description 8
- 238000009833 condensation Methods 0.000 description 8
- 229920005749 polyurethane resin Polymers 0.000 description 8
- 241000894006 Bacteria Species 0.000 description 7
- 239000002253 acid Substances 0.000 description 7
- 239000012948 isocyanate Substances 0.000 description 7
- 230000000844 anti-bacterial effect Effects 0.000 description 6
- 230000005494 condensation Effects 0.000 description 6
- 230000007423 decrease Effects 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000003431 cross linking reagent Substances 0.000 description 5
- 229910052731 fluorine Inorganic materials 0.000 description 5
- 239000011737 fluorine Substances 0.000 description 5
- 239000011259 mixed solution Substances 0.000 description 5
- 239000004677 Nylon Substances 0.000 description 4
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 4
- 239000002202 Polyethylene glycol Substances 0.000 description 4
- 229920000297 Rayon Polymers 0.000 description 4
- 229920002678 cellulose Polymers 0.000 description 4
- 239000001913 cellulose Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- 229920001778 nylon Polymers 0.000 description 4
- 229920001223 polyethylene glycol Polymers 0.000 description 4
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 4
- 239000004925 Acrylic resin Substances 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 238000005299 abrasion Methods 0.000 description 3
- 235000011054 acetic acid Nutrition 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
- 230000001070 adhesive effect Effects 0.000 description 3
- 150000001408 amides Chemical class 0.000 description 3
- 239000011247 coating layer Substances 0.000 description 3
- 230000006196 deacetylation Effects 0.000 description 3
- 238000003381 deacetylation reaction Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000011221 initial treatment Methods 0.000 description 3
- 238000010297 mechanical methods and process Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 239000002964 rayon Substances 0.000 description 3
- 230000009257 reactivity Effects 0.000 description 3
- 239000002759 woven fabric Substances 0.000 description 3
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
- 244000025254 Cannabis sativa Species 0.000 description 2
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 2
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 2
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- 241000233866 Fungi Species 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 230000001580 bacterial effect Effects 0.000 description 2
- 235000009120 camo Nutrition 0.000 description 2
- 235000005607 chanvre indien Nutrition 0.000 description 2
- 238000004891 communication Methods 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 235000019253 formic acid Nutrition 0.000 description 2
- 239000011487 hemp Substances 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N isopropyl alcohol Natural products CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 239000004310 lactic acid Substances 0.000 description 2
- 235000014655 lactic acid Nutrition 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- ZIUHHBKFKCYYJD-UHFFFAOYSA-N n,n'-methylenebisacrylamide Chemical class C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 description 2
- 229910052763 palladium Inorganic materials 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 229920002239 polyacrylonitrile Polymers 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 230000003578 releasing effect Effects 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- 238000010345 tape casting Methods 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 210000002268 wool Anatomy 0.000 description 2
- WHOZNOZYMBRCBL-OUKQBFOZSA-N (2E)-2-Tetradecenal Chemical compound CCCCCCCCCCC\C=C\C=O WHOZNOZYMBRCBL-OUKQBFOZSA-N 0.000 description 1
- RTTZISZSHSCFRH-UHFFFAOYSA-N 1,3-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC(CN=C=O)=C1 RTTZISZSHSCFRH-UHFFFAOYSA-N 0.000 description 1
- YQFIWRZWBBOPAF-UHFFFAOYSA-N 1,6-diisocyanatohexane;2-ethyl-2-(hydroxymethyl)propane-1,3-diol Chemical compound CCC(CO)(CO)CO.O=C=NCCCCCCN=C=O YQFIWRZWBBOPAF-UHFFFAOYSA-N 0.000 description 1
- UWFRVQVNYNPBEF-UHFFFAOYSA-N 1-(2,4-dimethylphenyl)propan-1-one Chemical compound CCC(=O)C1=CC=C(C)C=C1C UWFRVQVNYNPBEF-UHFFFAOYSA-N 0.000 description 1
- TUSDEZXZIZRFGC-UHFFFAOYSA-N 1-O-galloyl-3,6-(R)-HHDP-beta-D-glucose Natural products OC1C(O2)COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC1C(O)C2OC(=O)C1=CC(O)=C(O)C(O)=C1 TUSDEZXZIZRFGC-UHFFFAOYSA-N 0.000 description 1
- IVIDDMGBRCPGLJ-UHFFFAOYSA-N 2,3-bis(oxiran-2-ylmethoxy)propan-1-ol Chemical compound C1OC1COC(CO)COCC1CO1 IVIDDMGBRCPGLJ-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- MECNWXGGNCJFQJ-UHFFFAOYSA-N 3-piperidin-1-ylpropane-1,2-diol Chemical compound OCC(O)CN1CCCCC1 MECNWXGGNCJFQJ-UHFFFAOYSA-N 0.000 description 1
- 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 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- 241000254173 Coleoptera Species 0.000 description 1
- 241000238424 Crustacea Species 0.000 description 1
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 1
- 241000238557 Decapoda Species 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- 241000588724 Escherichia coli Species 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000001263 FEMA 3042 Substances 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 241000238814 Orthoptera Species 0.000 description 1
- LRBQNJMCXXYXIU-PPKXGCFTSA-N Penta-digallate-beta-D-glucose Natural products OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-PPKXGCFTSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 229920002873 Polyethylenimine Polymers 0.000 description 1
- 241000191940 Staphylococcus Species 0.000 description 1
- 241000191967 Staphylococcus aureus Species 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 241000223238 Trichophyton Species 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 229920006221 acetate fiber Polymers 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 239000011260 aqueous acid Substances 0.000 description 1
- 239000004566 building material Substances 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
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 210000002421 cell wall Anatomy 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 230000008094 contradictory effect Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000012258 culturing Methods 0.000 description 1
- 239000002781 deodorant agent Substances 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
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 1
- IQDGSYLLQPDQDV-UHFFFAOYSA-N dimethylazanium;chloride Chemical compound Cl.CNC IQDGSYLLQPDQDV-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000000174 gluconic acid Substances 0.000 description 1
- 235000012208 gluconic acid Nutrition 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-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
- 238000009981 jet dyeing Methods 0.000 description 1
- 239000012669 liquid formulation Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 229940044654 phenolsulfonic acid Drugs 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000011527 polyurethane coating Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000003405 preventing effect Effects 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000007763 reverse roll coating Methods 0.000 description 1
- 150000003376 silicon Chemical class 0.000 description 1
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- 208000017520 skin disease Diseases 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- 230000035900 sweating Effects 0.000 description 1
- 230000002522 swelling effect Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- LRBQNJMCXXYXIU-NRMVVENXSA-N tannic acid Chemical compound OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-NRMVVENXSA-N 0.000 description 1
- 229920002258 tannic acid Polymers 0.000 description 1
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- 239000004753 textile Substances 0.000 description 1
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- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
Landscapes
- Laminated Bodies (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は吸水性、水分の拡散性、水分の放出性に優れ
た性質を有する透湿性防水布帛に関する。Description: TECHNICAL FIELD The present invention relates to a moisture-permeable waterproof fabric having excellent properties of water absorption, water diffusion, and water release.
スキー、ジョギング、ゴルフ等で着用されるスポーツ
ウエアは雨水等がウエアを通して人体側に浸透すること
なく、一方、人体側から発散される汗及び汗の蒸気がウ
エアをとおしてすみやかに外部へ発散されることが好ま
しい。又下着類、スーツのような寝装類では、汗を速や
かに吸収し、それを放出することが望ましい。In sportswear worn for skiing, jogging, golfing, etc., rainwater does not penetrate to the human body through the wear, while sweat and sweat vapor radiated from the human body are quickly radiated to the outside through the wear. Preferably. Also, in the case of bedding such as underwear and suits, it is desirable to quickly absorb and release sweat.
製品の防水性は製品の望ましい吸水性および透湿性と
は相反する性質である。したがってこれら相反する性質
を満足させる試みとして、多数の微多孔を有するウレタ
ン樹脂層を配置した布帛や、透湿性を有するが無孔性の
ウレタン樹脂層を有する布帛が知られている。しかしな
がらウレタン樹脂層の透湿性や吸水性は乏しく、運動に
よる発汗量がウエアの樹脂層の透湿度を上回る場合や、
外気温度の低い場合、外気湿度が高い場合には、ウエア
の内部に、肉眼で見えるほどの汗の水滴が付着する。そ
のため、下着や皮膚を濡らし、不快感を与えるのみなら
ず、風邪の原因にもなる。Product waterproofing is a property that is inconsistent with the desired water absorption and moisture permeability of the product. Therefore, as an attempt to satisfy these contradictory properties, a fabric in which a large number of microporous urethane resin layers are arranged, and a fabric having a moisture-permeable but nonporous urethane resin layer are known. However, the moisture permeability and water absorption of the urethane resin layer are poor, and when the amount of sweat caused by exercise exceeds the moisture permeability of the resin layer of the wear,
When the outside air temperature is low or when the outside air humidity is high, water droplets of sweat that can be seen with the naked eye adhere to the inside of the wear. Therefore, it not only wets the underwear and the skin and gives discomfort but also causes a cold.
木綿やレーヨン等のセルロース系繊維は吸水性にすぐ
れている為に、下着や寝装具に古くから使用されてき
た。しかしながら、セルロース系繊維は吸水性にすぐれ
ているけれども吸収した水分の放出速度が小さい。した
がって、発汗した場合に繊維は汗の吸収により膨潤し、
汗を放出しないために着心地が悪い。一方、合成繊維は
吸水性に乏しいため、ポリエチレングリコールやメトキ
シメチル化ナイロンのような、親水性物質を繊維表面に
付与して吸水性を与えることが試みられてきた。しか
し、この繊維の吸水性は不十分であった。親水性物質を
多量に使用すると布帛の風合が著しく悪くなる。親水性
物質は洗濯を繰り返すことによって、布帛から次第に脱
落するという欠点があった。Cellulose fibers such as cotton and rayon have been used for underwear and bedding for a long time because of their excellent water absorption. However, although cellulosic fibers are excellent in water absorption, the release rate of absorbed water is small. Therefore, when sweating, the fibers swell due to sweat absorption,
It is not comfortable to release sweat. On the other hand, synthetic fibers have poor water absorption, and attempts have been made to impart water absorption by imparting a hydrophilic substance such as polyethylene glycol or methoxymethylated nylon to the fiber surface. However, the water absorption of this fiber was insufficient. If a large amount of the hydrophilic substance is used, the feeling of the fabric is significantly deteriorated. There was a drawback that the hydrophilic substance gradually dropped off from the fabric due to repeated washing.
本発明は従来の布帛に比べて吸水性、水分の拡散性、
水分の放出性に優れた性質を有する透湿性防水布帛の提
供を目的とする。The present invention is more water-absorbing than conventional fabrics, diffusibility of moisture,
An object of the present invention is to provide a moisture-permeable waterproof fabric having excellent properties of releasing moisture.
本発明の目的は、基布と、前記基布の表面に順次付与
された少なくとも2層からなる3000g/m2/24hours以上の
透湿度を有する防水性合成樹脂層からなり、かつ前記合
成樹脂層の少なくとも1層にキチン系物質が分散、含有
されている透湿性防水布帛によって達成される。An object of the present invention comprises a base fabric made of waterproof synthetic resin layer having a 3000 g / m 2 / 24hours or more moisture permeability of at least two layers which are sequentially applied to the surface of the base fabric, and the synthetic resin layer This is achieved by a moisture-permeable waterproof fabric in which a chitin-based substance is dispersed and contained in at least one layer.
本発明の透湿性防水布帛は基布をキチン系物質と合成
樹脂を含有する液でコーティングし、コーティングした
基布を加熱乾燥する方法によって製造することができ
る。The moisture-permeable waterproof fabric of the present invention can be produced by coating a base fabric with a liquid containing a chitin-based substance and a synthetic resin, and heating and drying the coated base fabric.
本出願で用いられる「キチン系物質」とはキチン、キ
チンの脱アセチル化化合物、すなわちキトサン、カルボ
キシル変性したキチン等を含むものとする。The "chitin-based substance" used in the present application includes chitin and a deacetylated compound of chitin, that is, chitosan, carboxyl-modified chitin, and the like.
キチンは、自然界に広く、また豊富に存在し、特に無
脊椎動物や菌類等にタンパク質との複合体としてふくま
れている。無脊椎動物のうち、エビ、カニなどの甲殻類
やカブトムシ、こおろぎなどの昆虫類に多量に含まれて
いる。また、菌類の細胞壁にも多く含まれている。これ
ら原材料からキチンを製造する方法は、たとえば、Jour
nal of Biological sciences Research,Vol 7.P168(19
54),Journal of Organic Chemistry,Vol 27,P1161(19
62)、およびFishery Technology,Vol 11,P50(1974)
等に開示されている。Chitin is widely and abundantly present in nature, and is included as a complex with proteins, particularly in invertebrates and fungi. Among invertebrates, it is contained in large amounts in crustaceans such as shrimp and crab, and insects such as beetles and crickets. It is also contained abundantly in cell walls of fungi. Methods for producing chitin from these raw materials are described, for example, in Jour
nal of Biological sciences Research, Vol 7.P168 (19
54), Journal of Organic Chemistry, Vol 27, P1161 (19
62), and Fishery Technology, Vol 11, P50 (1974)
Etc.
キチンはセルロースと類似した化学構造をもつが、セ
ルロースとちがって、結晶性にすぐれているため化学反
応性に強い抵抗があり、溶解、膨潤性が乏しいなど、セ
ルロースとは性質がかなり異なっており、セルロースそ
の他の多糖類に比べてその利用度は低い。したがって現
在ではキチンは大部分がキチン誘導体であるキトサンの
形で汚泥処理における凝集剤に使用されているにすぎな
い。Chitin has a similar chemical structure to cellulose, but unlike cellulose, it has excellent crystallinity and therefore has strong resistance to chemical reactivity, and has very different properties from cellulose, such as poor dissolution and swelling properties. And its utilization is lower than that of cellulose and other polysaccharides. Thus, chitin is currently only used as a flocculant in sludge treatment in the form of chitosan, which is largely a chitin derivative.
しかしながら本出願でいうキチン系物質は他の化合物
に比べて優れた他の性質を有する。すなわちキチン系物
質は生体適合性に優れているから、手術の際の縫合糸や
人工皮膚としての用途が期待されている。However, the chitin-based substance referred to in the present application has other excellent properties as compared with other compounds. That is, chitin-based substances are excellent in biocompatibility, and therefore, are expected to be used as sutures or artificial skins during surgery.
又キチン系物質は、大腸菌、白癬菌、ブドウ状球菌な
どにたいする抗菌性にすぐれているため、布帛に抗菌性
を与えることができる。また、生体適合性にもすぐれて
いるから、皮膚障害をおこさない。In addition, the chitin-based substance is excellent in antibacterial properties against Escherichia coli, Trichophyton, Staphylococcus and the like, and thus can impart antibacterial properties to fabrics. In addition, since it has excellent biocompatibility, it does not cause skin disorders.
本発明者らは、キチン系物質を合成樹脂とともに布帛
に付着させると、キチン系物質を有する吸水性等の優れ
た性質によってその布帛の吸水性、水分放出性が著しく
向上することを見出した。The present inventors have found that when a chitin-based material is attached to a fabric together with a synthetic resin, the water-absorbing property and water-releasing property of the fabric are significantly improved due to excellent properties such as water absorption having the chitin-based material.
本発明の布帛に用いられる基布としては、織物、編
物、不織布等を用いることができる。基布を構成する繊
維としては、木綿、麻のような天然繊維、ビスコースレ
ーヨン、キュプラアンモニウムレーヨン、アセテートの
ような化学繊維、ポリアミド、ポリエステル、ポリアク
リロニトリルのような合成繊維があげられる。これら
は、ステープル、フィラメントとして使用される。As the base fabric used for the fabric of the present invention, a woven fabric, a knitted fabric, a nonwoven fabric, or the like can be used. Examples of the fibers constituting the base fabric include natural fibers such as cotton and hemp, chemical fibers such as viscose rayon, cupra ammonium rayon, and acetate, and synthetic fibers such as polyamide, polyester, and polyacrylonitrile. These are used as staples and filaments.
キチン系物質は、繊維からの脱落を防止するために、
合成樹脂とともに用いられる。チン系物質は合成樹脂の
中に均一に分散されてから用いられる。したがって、合
成樹脂自体が吸水性がない場合でも、キチン系物質に接
触した水分は速やかに合成樹脂の中に吸収されて拡散
し、又合成樹脂の中に吸収された水分は速やかに大気中
へ放出される。合成樹脂が良好な透湿性を有する場合に
は、この吸収および放出がさらに加速する。Chitin-based substances are used to prevent the fibers from falling off.
Used with synthetic resins. The tin-based material is used after being uniformly dispersed in the synthetic resin. Therefore, even when the synthetic resin itself has no water absorption, the moisture in contact with the chitin-based substance is quickly absorbed and diffused into the synthetic resin, and the moisture absorbed in the synthetic resin is quickly released into the atmosphere. Released. If the synthetic resin has good moisture permeability, this absorption and release is further accelerated.
本発明のキチン系物質として、キチンをそのまゝでも
用いることができるが、その誘導体としても用いること
ができる。キチン誘導体としては脱アセチル化度50%以
上のキチン(キトサン)、カルボキシル変性したキチン
が好ましい。Although chitin can be used as it is as the chitin-based substance of the present invention, it can also be used as a derivative thereof. As the chitin derivative, chitin (chitosan) having a degree of deacetylation of 50% or more and carboxyl-modified chitin are preferable.
ポリウレタン樹脂、ポリアクリル樹脂、ポリビニルク
ロライド樹脂、変性酸アミド樹脂、ポリアクリル酸エス
テル樹脂、ポリビニルアルコール樹脂等を本発明におけ
る基布へ付与される合成樹脂として用いることができ
る。A polyurethane resin, a polyacryl resin, a polyvinyl chloride resin, a modified acid amide resin, a polyacrylate resin, a polyvinyl alcohol resin, or the like can be used as the synthetic resin applied to the base fabric in the present invention.
キチン系物質と合成樹脂を含む液が基布の表面にコー
ティングする場合には、3,000g/m2/24hour以上の透湿度
を有する合成樹脂を用いると好ましい。合成樹脂に透湿
性を与える方法としては機械的方法と化学的方法の2つ
の方法を用いることができる。前記機械的方法としては
さらに乾式法と湿式法の2つを用いることができる。When the liquid containing the chitin-based material and synthetic resin is coated on the surface of the base fabric, preferably using a synthetic resin having a moisture permeability of more than 3,000g / m 2 / 24hour. As a method for imparting moisture permeability to the synthetic resin, two methods, a mechanical method and a chemical method, can be used. As the mechanical method, two methods, a dry method and a wet method, can be further used.
乾式法としてはキチン系物質、合成樹脂および有機溶
媒を含む液を用意し、この液を目的とする布帛のタイプ
に応じて適切に基布にコーティングし、有機溶媒を蒸発
させて布帛中に複数の微細な連通孔を形成させるため
に、コーティング布を乾燥する方法を用いることができ
る。湿式法としては、キチン系物質、合成樹脂および溶
媒を含む液を用意し、この液を目的とする布帛のタイプ
に応じて適切に基布にコーティングし、布帛中に複数の
微細な連通孔を形成するために、合成樹脂中の溶媒を溶
出させて合成樹脂を凝固させることができる液にコーテ
ィング布を浸漬する方法を用いることができる。As a dry method, a liquid containing a chitin-based substance, a synthetic resin, and an organic solvent is prepared, and this liquid is appropriately coated on a base fabric according to the type of the intended cloth, and the organic solvent is evaporated to form a plurality of liquids in the cloth. In order to form the fine communication holes, a method of drying the coating cloth can be used. As a wet method, a liquid containing a chitin-based substance, a synthetic resin, and a solvent is prepared, and this liquid is appropriately coated on a base cloth according to a type of a target cloth, and a plurality of fine communication holes are formed in the cloth. In order to form, a method of immersing the coating cloth in a liquid that can elute the solvent in the synthetic resin and solidify the synthetic resin can be used.
合成樹脂に透湿性を与える化学的方法としては、ポリ
エチレングリコールやアミノ酸樹脂等の親水性樹脂を合
成樹脂に混合する方法、と前記親水性樹脂と疎水性樹脂
の共重合体を用いる方法があげられる。Examples of the chemical method for imparting moisture permeability to the synthetic resin include a method of mixing a hydrophilic resin such as polyethylene glycol or an amino acid resin with the synthetic resin, and a method of using a copolymer of the hydrophilic resin and the hydrophobic resin. .
基布と、基布の表面に順次付与された少くとも2層の
合成樹脂層を含んで成り、前記少くとも2層の合成樹脂
層内の少くとも1層にキチン系物質が含有されている布
帛においては、キチン系物質と合成樹脂を含んで成る量
中のキチン系物質の割合は少くとも0.5重量%、より好
ましくは1重量%であると好ましく、一方基布に対する
合成樹脂の割合は10重量%と80重量%の間、より好まし
くは15重量%から70重量%であると好ましい。合成樹脂
層と基布間、あるいは合成樹脂層相互の接着力を増すた
めに、架橋剤および架橋剤と反応性を有する合成樹脂を
用いることが好ましい。架橋剤と反応性を有する合成樹
脂としては、ポリウレタン樹脂、ポリアクリル酸エステ
ル樹脂、変性酸アミド樹脂、ポリビニルアルコール樹脂
が好ましい。It comprises a base cloth and at least two synthetic resin layers sequentially applied to the surface of the base cloth, and at least one of the at least two synthetic resin layers contains a chitin-based substance. In fabrics, the proportion of the chitin-based material in the amount comprising the chitin-based material and the synthetic resin is preferably at least 0.5% by weight, more preferably 1% by weight, while the ratio of the synthetic resin to the base fabric is 10%. It is preferred that it is between 15% and 80% by weight, more preferably between 15% and 70% by weight. In order to increase the adhesive force between the synthetic resin layer and the base cloth or between the synthetic resin layers, it is preferable to use a cross-linking agent and a synthetic resin having reactivity with the cross-linking agent. As the synthetic resin having reactivity with the crosslinking agent, a polyurethane resin, a polyacrylate resin, a modified acid amide resin, and a polyvinyl alcohol resin are preferable.
架橋剤としては、エピクロルヒドリン、エチレングリ
コールジグリシジルエーテル、ポリエチレングリコール
グリシジルエーテル、トリメチロールプロパントリグリ
シジルエーテル、グリセリンジグリシジルエーテル、1,
6ヘキサンジオールジルエーテルのエポキシ化合物、2,4
トリレンジイソシアネート、ヘキサメチレンジイソシア
ネート、メチレンビスフェニルイソシアネート、メチレ
ンビス4シクロヘキシリックイソシアネート、イソフォ
ロンジイソシアネート、トリメチロールロパン−ヘキサ
メチレンジイソシアネート等のイソシアネート化合物、
エチレングリコール、トリメチロールプロパン、グリセ
リン、ポリオキシエチレングリコールなどのポリオール
化合物、N,Nメチレンビスアクリルアミドなどのビスア
クリルアミド化合物、ポリエポキシドとアクリル酸また
はメタアクリル酸を反応させて得られるジもしくはトリ
アクリル酸またはメタアクリル酸エステル化合物等があ
る。Examples of the crosslinking agent include epichlorohydrin, ethylene glycol diglycidyl ether, polyethylene glycol glycidyl ether, trimethylolpropane triglycidyl ether, glycerin diglycidyl ether, 1,
6 epoxy compound of hexanediol diether, 2,4
Isocyanate compounds such as tolylene diisocyanate, hexamethylene diisocyanate, methylene bisphenyl isocyanate, methylene bis 4 cyclohexyl isocyanate, isophorone diisocyanate, trimethylol lopan-hexamethylene diisocyanate,
Ethylene glycol, trimethylol propane, glycerin, polyol compounds such as polyoxyethylene glycol, N, bisacrylamide compounds such as methylenebisacrylamide, di- or triacrylic acid obtained by reacting polyepoxide with acrylic acid or methacrylic acid or Examples include methacrylate compounds.
架橋剤は合成樹脂に対して通常0.3〜10重量%、好ま
しくは0.5〜5重量%用いられる。The crosslinking agent is used usually in an amount of 0.3 to 10% by weight, preferably 0.5 to 5% by weight, based on the synthetic resin.
基布をキチン系物質と合成樹脂を含有する液でコーテ
ィングすることによって作られる布帛においては、布帛
が合成樹脂層で被覆されているので優れた防水性を有
し、且つキチン系物質が合成樹脂の中に含まれているの
で、得られた布帛は優れた吸水性と水分の拡散性および
放水性を有する。さらに良好な透湿性を有する合成樹脂
が用いられた場合には前記特徴が強化される。In a fabric made by coating a base cloth with a liquid containing a chitin-based material and a synthetic resin, the fabric is covered with a synthetic resin layer, so that the fabric has excellent waterproof properties, and the chitin-based material is made of a synthetic resin. The resulting fabric has excellent water absorption, water diffusion and water release. If a synthetic resin having good moisture permeability is used, the above characteristics are enhanced.
例えば層中に多数の貫通孔を設けることによって得る
ことができる、3,000g/m2/24hours以上の透湿度を有す
る合成樹脂から成る層は、キチン系物質と合成樹脂を含
んで成る層の上にコーティングして用いてもよい。又キ
チン系物質と合成樹脂を含んで成る層は1層でも2層以
上用いてもよい。For example, can be obtained by providing a large number of through-holes in the layer, the layer made of a synthetic resin having the above moisture permeability 3,000g / m 2 / 24hours, the upper layer comprising a chitin-based material and synthetic resin May be used after coating. The layer containing the chitin-based material and the synthetic resin may be one layer or two or more layers.
合成樹脂層の厚さは任意に設定すればよい。合成樹脂
層を複数設ける場合は、1つの層の厚みを2〜30μ、よ
り好ましくは5〜15μにする。The thickness of the synthetic resin layer may be set arbitrarily. When a plurality of synthetic resin layers are provided, the thickness of one layer is set to 2 to 30 μ, more preferably 5 to 15 μ.
撥水性をさらに向上させるために、布帛に弗素系撥水
剤等の撥水剤を付与することが好ましい。In order to further improve the water repellency, it is preferable to add a water repellent such as a fluorine-based water repellent to the fabric.
以下本発明の布帛の製造方法を説明する。 Hereinafter, the method for producing the fabric of the present invention will be described.
最初にキチン系物質を希酸の水溶液に溶解する。酸と
しては、酢酸、乳酸、蟻酸、コハク酸、グルコン酸等が
あり、蟻酸が好ましい。酸の濃度は1〜10重量%がこの
ましい。酸の水溶液中のキチン系物質の濃度は、溶解
性、粘度などを考慮して決定されるが、0.3〜1重量%
がより好ましい。First, a chitin-based substance is dissolved in an aqueous solution of a dilute acid. Examples of the acid include acetic acid, lactic acid, formic acid, succinic acid, and gluconic acid, and formic acid is preferred. The acid concentration is preferably 1 to 10% by weight. The concentration of the chitin-based substance in the aqueous acid solution is determined in consideration of solubility, viscosity, etc.
Is more preferred.
基布をキチン系物質と合成樹脂を含有する液でコーテ
ィングし、コーティングした基布を加熱乾燥して得られ
る布帛を製造する場合には、例えば最初に前記キチン系
物質の液が有機溶媒によって溶解された合成樹脂と混合
され、この混合液に乳化剤を加えることによってエマル
ジョンを形成する。さらに顔料、アルミニウム等の金属
粉末、カーボン、セラミックなどを添加してもよい。When producing a fabric obtained by coating a base cloth with a liquid containing a chitin-based substance and a synthetic resin and heating and drying the coated base cloth, for example, the liquid of the chitin-based substance is first dissolved in an organic solvent. The mixed resin is mixed with an emulsifier to form an emulsion. Further, pigments, metal powders such as aluminum, carbon, ceramics and the like may be added.
混合体を布帛表面に被覆する方法として、例えば混合
溶液を直接ナイフコーターによりコーティングする方
法、バーコーターにより一定の厚みにコーティングする
方法、リバースコーターやグラビアコーターによりコー
ティングする方法がある。As a method of coating the mixture on the surface of the fabric, for example, there are a method of directly coating the mixed solution with a knife coater, a method of coating the mixed solution to a predetermined thickness with a bar coater, and a method of coating with a reverse coater or a gravure coater.
被覆したあと、乾燥する。乾燥温度は50〜100℃が好
ましい。樹脂と布帛、樹脂同志の接着性をあげるため、
乾燥後さらに100〜130℃で加熱することが好ましい。After coating, dry. The drying temperature is preferably from 50 to 100 ° C. In order to increase the adhesiveness between resin and fabric and resin,
After drying, it is preferable to further heat at 100 to 130 ° C.
合成樹脂自体に透湿性を与えるために前述のように機
械的方法又は化学的方法を用いるとよい。As described above, a mechanical method or a chemical method may be used to impart moisture permeability to the synthetic resin itself.
混合液で基布をコーティングする前に基布に撥水剤を
付与すると好ましい。さらに最初に透湿性を有し且つ撥
水剤を含む合成樹脂を基布にコーティングし、得られた
コーティング層の上にキチン系物質を含む合成樹脂をコ
ーティングしてもよい。これとは逆に最初にキチン系物
質を含む合成樹脂を基布にコーティングし、得られたコ
ーティング層の上に透湿性を有し且つ撥水剤を含む合成
樹脂をコーティングしてもよい。It is preferable to apply a water repellent to the base fabric before coating the base fabric with the mixed solution. Further, first, a synthetic resin having moisture permeability and containing a water repellent may be coated on the base fabric, and a synthetic resin containing a chitin-based substance may be coated on the obtained coating layer. Conversely, a synthetic resin containing a chitin-based substance may be first coated on the base fabric, and the resultant coating layer may be coated with a synthetic resin having moisture permeability and containing a water repellent.
本発明によるこのようにして得られた透湿性防水布帛
はさらに他の処理を施さなくても本発明の目的とする性
能を発揮することができる。しかしキチン系物質と基布
との結合力をあげるために固着処理を施すと好ましい。
固着剤は、布帛に該当する繊維の素材に応じて選択使用
され、たとえば、綿、麻、レーヨンなどのウール以外の
天然素材に対しては、ポリアミン型、ポリビニルアミ
ン、ポリアクリルニトリル系重合物、ポリエチレンイミ
ンを4級化したものなどのポリカチオン型その他が有
り、ウール素材に対しては、含金属合成タンニン誘導体
等が有り、ナイロン素材に対しては、タンニン酸、フェ
ノールスルホン酸ホルマリン縮合物等が挙げられる。The moisture-permeable waterproof fabric thus obtained according to the present invention can exhibit the intended performance of the present invention without further treatment. However, it is preferable to carry out a fixing treatment in order to increase the bonding strength between the chitin-based substance and the base cloth.
The fixing agent is selected and used according to the material of the fiber corresponding to the fabric.For example, for natural materials other than wool such as cotton, hemp, and rayon, polyamine type, polyvinylamine, polyacrylonitrile-based polymer, There are polycation types such as quaternized polyethyleneimine, etc. For wool materials, there are metal-containing synthetic tannin derivatives, etc. For nylon materials, tannic acid, phenolsulfonic acid formalin condensate, etc. Is mentioned.
第1図〜第4図は本発明による、基布と、基布の表面
に順次付与された少くとも2層の合成樹脂層から成り、
該少くとも2層の合成樹脂層内の少くとも1層にキチン
系物質が含有されている布帛の各種実施例を示す断面図
である。FIGS. 1 to 4 consist of a base cloth according to the invention and at least two synthetic resin layers successively applied to the surface of the base cloth,
FIG. 6 is a cross-sectional view showing various examples of a cloth in which at least one of the at least two synthetic resin layers contains a chitin-based substance.
第1図において1は基布、2は撥水剤とイソシアネー
ト化合物を含む部分、3は透湿性を有する合成樹脂層、
4はキチン系物質と合成樹脂を含有する層であり、樹脂
層が2層である場合の実施例を示す。第2図は樹脂層が
3層であり、中間層にキチン系物質が含まれている実施
例の布帛であり、第3図は樹脂層が3層であり、外側層
にキチン系物質が含まれている実施例の布帛であり、第
4図は樹脂層が3層であり、中間層と外側層にキチン系
物質が含まれている実施例の布帛である。図中の複数の
極小線6はキチン系物質を示す。合成樹脂の層は2層以
上あればよく、例えば5層にしてもよい、又第1図にお
いて基布1は経糸1aおよび緯糸1bから成る織物で示して
いるが、編物、不織布等を基布として用いてもよい。In FIG. 1, 1 is a base cloth, 2 is a portion containing a water repellent and an isocyanate compound, 3 is a synthetic resin layer having moisture permeability,
Reference numeral 4 denotes a layer containing a chitin-based substance and a synthetic resin, and shows an example in which the number of resin layers is two. FIG. 2 shows an example of a fabric having three resin layers and an intermediate layer containing a chitin-based substance, and FIG. 3 shows a three-layer resin layer containing an chitin-based substance in an outer layer. FIG. 4 shows a fabric having three resin layers and an intermediate layer and an outer layer containing a chitin-based material. A plurality of minimum lines 6 in the figure indicate chitin-based substances. The number of layers of the synthetic resin may be two or more, for example, five layers. In FIG. 1, the base fabric 1 is shown as a woven fabric comprising a warp 1a and a weft 1b. May be used.
第1図〜第4図に示された布帛が基布を外側にして用
いた場合には、雨水等の浸透は合成樹脂層で防がれ、層
4、あるいは層4および/又は層5内に配置されたキチ
ン系物質の優れた吸水性のために、汗の蒸気は速やかに
吸収され、透湿性を有する層3を通って放出される。し
たがって例えばスポーツウエアのような布帛の内側に結
露が発生することがない。When the fabric shown in FIGS. 1 to 4 is used with the base fabric on the outside, penetration of rainwater or the like is prevented by the synthetic resin layer, and the layer 4 or the layer 4 and / or the layer 5 Due to the excellent water absorption of the chitin-based substance arranged in the water vapor, the sweat vapor is quickly absorbed and released through the moisture-permeable layer 3. Therefore, for example, dew condensation does not occur inside a cloth such as sportswear.
発生した汗の量が層3の透湿性と比べて大きい場合、
あるいは汗の蒸気の放出が高湿度の雰囲気中で充分でな
い場合には、汗の蒸気はキチン系物質を含有する大容量
の層中に吸収されて拡散し、其後汗の蒸気は逐次布帛か
ら放出されることになる。したがってこの場合において
もスポーツウエア内での結露の発生を防止することがで
きる。If the amount of generated sweat is large compared to the moisture permeability of the layer 3,
Alternatively, if the release of sweat vapor is not sufficient in an atmosphere of high humidity, the sweat vapor is absorbed and diffused into the large-capacity layer containing the chitin-based substance, and then the sweat vapor is sequentially removed from the fabric. Will be released. Therefore, also in this case, the occurrence of dew condensation in the sportswear can be prevented.
以下本発明の各種実施例により、本発明を詳述する。 Hereinafter, the present invention will be described in detail with reference to various examples of the present invention.
参考例1及び2 綿の綾織物(目付120g/m2、40番手 経緯密度190本/i
n)を次の要領で1次処理を行った。酢酸水溶液に脱ア
セチル化度80%以上のキトサン(大日精化工業社製:ダ
イキトサン)を濃度0.5%となる様に添加しディスパー
にて完全に溶解させる。このキトサン水溶液に下記配合
剤を加えて処理液を作成する。Reference Examples 1 and 2 Cotton twill fabric (basis weight 120 g / m 2 , 40 count, weft density 190 yarns / i
n) was subjected to primary treatment in the following manner. Chitosan having a degree of deacetylation of 80% or more (manufactured by Dainichi Seika Kogyo Co., Ltd .: dichitosan) is added to the acetic acid aqueous solution so as to have a concentration of 0.5%, and completely dissolved with a disper. A treatment liquid is prepared by adding the following compounding agent to this chitosan aqueous solution.
配合液中の各薬剤は、各々、変性酸アミド樹脂(三木
理研社製:リケンレジンRJ−36)、反応性特殊シリコン
誘導体(大原パラジウム社製:パラソルブ272)、有機
アミン系触媒(大原パラジウム社製:パラキャット
P)、エポキシシリコーン化合物(大日本インキ化学工
業社製:ディックシリコンソフナー200)を用いる。 Each of the chemicals in the blended liquid is a modified acid amide resin (manufactured by Miki Riken: Riken Resin RJ-36), a reactive special silicon derivative (manufactured by Ohara Palladium: Parasolve 272), and an organic amine catalyst (manufactured by Ohara Palladium) : Paracat P) and an epoxy silicone compound (Dick Silicon Softener 200 manufactured by Dainippon Ink and Chemicals, Inc.).
上記配合液中に綿素材からなる基布を室温にて3秒間
浸漬し絞り率100%となる様マングルで絞ったのち、120
℃60秒間加熱処理を施す。この1次処理した基布の内外
にキトサンを強固に固着処理させる為に2次処理を行な
う。すなわちジメチルアンモニウムクロライド(日清紡
績社製:ダンフィックス125)の1%水溶液に2次処理
の対象となる基布を1次処理と同様の室温にて3秒間浸
漬処理する。この様にして得られた布帛の特性を確認す
る為に抗菌性試験(菌数測定法)、吸水速度試験(JIS
L−1096 A法)を行った。After immersing a base cloth made of a cotton material in the above-mentioned mixed solution at room temperature for 3 seconds and squeezing with a mangle so that the squeezing rate becomes 100%, 120
Heat treatment at 60 ° C for 60 seconds. A secondary treatment is performed to firmly fix the chitosan inside and outside of the primary treated base cloth. That is, the base cloth to be subjected to the secondary treatment is immersed in a 1% aqueous solution of dimethylammonium chloride (manufactured by Nisshinbo Industries: Danfix 125) at room temperature for 3 seconds as in the primary treatment. In order to confirm the characteristics of the fabric thus obtained, an antibacterial test (microbial count method) and a water absorption rate test (JIS
L-1096 A method).
菌数測定は下記抗菌防臭加工製品の加工効果評価試験
マニュアル・菌数測定法(繊維製品衛生加工協議会、昭
和63年)によって行った。The number of bacteria was measured by the following manual for evaluating the effect of processing on antibacterial and deodorant processed products and the method for measuring the number of bacteria (Textile Sanitary Processing Council, 1988).
滅菌した液体ブイヨンに下記の菌を懸濁させ、この液
を0.2gの試験片上に0.2ml接種(菌数は約28万個)し、
温度37℃で18時間培養した後、取り出す。培養前後の試
験片上の生菌数を測定し、下記の計算式により菌数の増
減値及び増減値差を算出する。The following bacteria are suspended in a sterilized liquid broth, and 0.2 ml of this solution is inoculated on a 0.2 g test piece (the number of bacteria is about 280,000).
After culturing at a temperature of 37 ° C. for 18 hours, take out. The number of viable bacteria on the test piece before and after the culture is measured, and the increase / decrease value of the number of bacteria and the difference between the increase / decrease values are calculated by the following formula.
試 験 菌:黄色ぶどう状球菌 Staphylococcus aur
eus ATCC 6538P(IFO 12732) 試験片質量:0.2g 培養温度・時間:37℃×18h 洗濯方法:JIS L 0217,103号 菌数増減値差=無加工試料の菌数増減値−加工試料の
菌数増減値 ** 無加工試料として綿標準白布を用いた。Test bacteria: Staphylococcus aur
eus ATCC 6538P (IFO 12732) Test piece mass: 0.2g Culture temperature / time: 37 ℃ × 18h Washing method: JIS L 0217,103 Bacterial count increase / decrease difference = Bacterial count increase / decrease value of unprocessed sample−Bacterial count increase / decrease value of processed sample ** Cotton standard white cloth was used as the unprocessed sample.
参考例3及び4、対照例1及び2 ナイロンの加工糸織物(目付100g/m2 70d、経緯密度
200本/in)の染色布に対して、参考例1及び2と同様に
調整した0.5%キトサン水溶液を用い下記配合液を作成
して液流染色機中にて60℃10分間の浴中処理を行ない遠
心脱水機により、絞り率120%となる様絞ったのち、120
℃90秒間加熱処理を施した。Reference Examples 3 and 4, Comparative Examples 1 and 2 Processed yarn woven fabric of nylon (100 g / m 2 70d, basis density
For 200 dyes / in), the following formulation was prepared using a 0.5% aqueous solution of chitosan prepared in the same manner as in Reference Examples 1 and 2, and treated in a bath at 60 ° C. for 10 minutes in a jet dyeing machine. And then squeezed by a centrifugal dehydrator to a squeezing ratio of 120%.
Heat treatment was performed at 90 ° C. for 90 seconds.
この1次処理した機布の内外に、キトサンを強固に固
着する為に2次処理を行なう。すなわち芳香族スルホン
酸化合物(日華化学社製:サンライフTN)の0.5%水溶
液に1次処理した基布を室温にて3秒間浸漬処理する。
参考例3及び参考例4、対照例1及び対照例2にて得ら
れた布帛に対し参考例1及び2と同様の性能試験を行っ
た。結果を第1表に示す。 Secondary processing is performed on the inside and outside of the primary-treated fabric to firmly fix chitosan. That is, the base fabric that has been subjected to the primary treatment in a 0.5% aqueous solution of an aromatic sulfonic acid compound (manufactured by Nichika Chemical Co., Ltd .: Sun Life TN) is immersed for 3 seconds at room temperature.
The same performance tests as those in Reference Examples 1 and 2 were performed on the fabrics obtained in Reference Examples 3 and 4, and Comparative Examples 1 and 2. The results are shown in Table 1.
実施例1及び2、比較例1 ナイロン織物(70d、経、緯計210本/in)製の染色布
を、弗素系撥水剤(住友スリーエム社:(FC 232を水10
0部に対し2部の割合の濃度のもの)および接着剤とし
てのイソシアネート化合物(武田薬品工業社製:タケネ
ートB830Wを前記弗素系撥水剤に対して10%)からなる
混合液中に浸漬した後、160℃、60秒の加熱処理を行
い、150゜、線圧10トン(幅2000mm)の熱カレンダーで
布帛の片面に平滑性を付与するための熱処理を施し、通
気度(フラジール法)約15cc/cm2・秒の撥水製布帛を得
た(第1層の形成)。一方、W/O型ポリウレタン樹脂エ
マルジョン(三洋化成工業社製:サンプレンUE−1000
N)100部、トルエン40部、メチルエチルケトン20部、水
10部、弗素系撥水剤(前掲)20部及びイソシアネート化
合物(大日本インキ化学社製:バーノックDN950)5部
の混合液を調整し、この液を前記撥水処理及び熱カレン
ダー処理した布帛に湿潤状態の付着重量が30g/m2になる
ようナイフコート法を用いて塗布し乾燥状態で6.0g/m2
の付着重量の多孔質の透湿性防水層(第2層)を形成し
た。次いで酢酸と乳酸の混合比率が1:1の10%希酸溶液
を作り、その溶液の中へ脱アセチル化度80%のキチン
(片倉チッカリン社製:キトサンA)を0.5%量添加
し、24時間膨潤させたのちディスパーにて撹拌溶解させ
たキチン希酸溶液を55部、W/O型ポリウレタン樹脂エマ
ルジョン(大日精化工業社精:ハイムレンX−3038)を
100部、メチルエチルケトン20部、トルエン20部、イソ
シアネート化合物(前掲)1.5部からなる混合液を調整
し、この液を前記の第2層上にクリアランスを100μm
に設定したバーコーターを用いて湿潤状態で100g/m2に
なるように塗布しオーブン中で約70℃2分間加熱乾燥
し、乾燥状態で15g/m2の付着重量の多孔質の吸水性ポリ
ウレタン/キトサン膜層(第3層)を形成した。更に耐
摩耗性の改善及び装飾効果の向上を図るためW/O型ウレ
タン樹脂エマルジョン(三洋化成工業社製:サンプレン
UE 1000N)100部、メチルエチルケトン20部、トルエン2
0部、前記0.5%キトサン希酸溶液40部、イソシアネート
化合物(前掲)3部、有機顔料少量からなる混合液を調
製し、これを前記の第3層上にナイフコート法を用い
て、湿潤状態で40g/m2乾燥状態で8.0g/m2になるよう塗
布し、オーブン中で80℃、2分間乾燥して最内層(第4
図)を得た。次いで各層ん樹脂間及び布帛との接着性を
より強硬にするために120℃2分間加熱して仕上げセッ
トを行った。 Examples 1 and 2, Comparative Example 1 A dyed cloth made of nylon fabric (70d, longitude, total of 210 lines / in) was coated with a fluorine-based water repellent (Sumitomo 3M Co., Ltd .;
It was immersed in a mixture of an isocyanate compound (taken by Takeda Pharmaceutical Co., Ltd .: Takenate B830W, 10% with respect to the fluorine-based water repellent) as an adhesive. Thereafter, a heat treatment is performed at 160 ° C. for 60 seconds, and a heat calender is applied at 150 ° C. and a linear pressure of 10 tons (2000 mm in width) to impart smoothness to one side of the fabric. A water-repellent cloth of 15 cc / cm 2 · second was obtained (formation of the first layer). On the other hand, W / O type polyurethane resin emulsion (manufactured by Sanyo Chemical Industries, Ltd .: Samprene UE-1000)
N) 100 parts, toluene 40 parts, methyl ethyl ketone 20 parts, water
A liquid mixture of 10 parts, 20 parts of a fluorine-based water repellent (described above) and 5 parts of an isocyanate compound (manufactured by Dainippon Ink and Chemicals, Inc .: Vernock DN950) was prepared. Apply using knife coating method so that the adhesion weight in the wet state is 30 g / m 2 and 6.0 g / m 2 in the dry state
To form a porous moisture-permeable waterproof layer (second layer) having an adhesion weight of. Next, a 10% dilute acid solution having a mixing ratio of acetic acid and lactic acid of 1: 1 was prepared, and chitin (Chitosan A, manufactured by Katakura Tikkalin Co., Ltd.) having a degree of deacetylation of 80% was added to the solution in a 0.5% amount. 55 parts of a chitin dilute acid solution which was swelled for a time and then stirred and dissolved with a disper, and a W / O type polyurethane resin emulsion (Dainichi Seika Kogyo Co., Ltd .: Heimulen X-3038) was added.
A mixed solution consisting of 100 parts, 20 parts of methyl ethyl ketone, 20 parts of toluene and 1.5 parts of an isocyanate compound (described above) was prepared, and this solution was allowed to have a clearance of 100 μm on the second layer.
Absorbent polyurethane coating dried by heating to about 70 ° C. 2 minutes in an oven so as to 100 g / m 2 in the wet state, the porous attachment weight of 15 g / m 2 in a dry state using a bar coater set at / A chitosan film layer (third layer) was formed. In order to further improve the wear resistance and the decorative effect, a W / O type urethane resin emulsion (manufactured by Sanyo Chemical Industries, Ltd .: Samprene)
UE 1000N) 100 parts, methyl ethyl ketone 20 parts, toluene 2
A mixture of 0 parts, 40 parts of the 0.5% chitosan dilute acid solution, 3 parts of the isocyanate compound (described above), and a small amount of an organic pigment was prepared, and the mixture was wetted on the third layer by knife coating. in coated so as to be 8.0 g / m 2 at 40 g / m 2 dry, 80 ° C. in an oven, dried innermost layer 2 minutes (4
Figure). Next, in order to make the adhesiveness between the resin layers and between the resin layers and the fabric even harder, finishing was performed by heating at 120 ° C. for 2 minutes.
本発明中の布帛に対するキチン量は実施例1では1.04
%、実施例2の布帛では2.08%、比較例1では0.3%と
なる様脱アセチル化キチン水溶液の量を変えた。The amount of chitin for the fabric in the present invention was 1.04 in Example 1.
%, The amount of the aqueous solution of deacetylated chitin was changed so as to be 2.08% for the fabric of Example 2, and 0.3% for Comparative Example 1.
得られた多孔質の吸湿、透湿性防水布の特性を確認す
るために、耐水圧(JIS L 1092に基ずく水圧mm)、撥水
性(JIS L 1092に基ずく%)、透湿度(JIS L 1099に基
ずくg/m2/24hrs.)、耐摩耗性(級)、結露状態(水滴
観察)、吸湿性(%)及び吸水速度(JIS L 1096A)を
調べた。以上の各測定結果を第2表に示す。In order to confirm the characteristics of the obtained porous moisture-absorbing and moisture-permeable waterproof cloth, water resistance (water pressure mm based on JIS L 1092), water repellency (% based on JIS L 1092), moisture permeability (JIS L 1099 based Nuisance g / m 2 / 24hrs.) , abrasion resistance (grade), dew condensation (water droplets observed), was examined hygroscopicity (%) and absorption rate (JIS L 1096A). Table 2 shows the results of the above measurements.
ここで耐摩耗試験は乾燥状態及び湿潤状態にある綿布
で、試供布綿に200gの荷重を与え500回往復運動させた
時の試供布の樹脂面の状態を5段階に評価した。すなわ
ち、 異常が認められない。 …5級 若干の擦過痕が認められる。 …4級 かなりの擦過痕が認められる。 …3級 若干の剥離が認められる。 …2級 かなりの剥離が認められる。 …1級 である。Here, in the abrasion resistance test, the state of the resin surface of the test sample when the test sample cotton was reciprocated 500 times by applying a load of 200 g to the test sample cotton was evaluated on a 5-point scale. That is, no abnormality is observed. … Class 5 Some scratch marks are observed. … Class 4 Considerable scratch marks are observed. ... Grade 3 Some peeling is observed. … Class 2 Considerable peeling is observed. ... First grade.
また結露状態の試験は、外気温度20±1℃、湿度80
(%)RHの気流条件を設定した人工気候室中にて、40±
1℃の温調の可能なウォーターバスの温湯面上約2cmの
位置に加工布のコーティング面が湯面側になるように覆
い20分間放置する。この場合、加工布と温湯との間に外
気の流入がないように容器壁にて密閉する。20分間放置
後コーティング層表面の水滴(結露)状態を観察し次の
ように分類した。In addition, the test of the dew condensation condition was performed at an outside air temperature of 20 ± 1 ° C and a humidity of 80.
(%) 40 ± in a climate chamber with RH airflow conditions
Cover the work cloth at about 2 cm above the hot water surface of a water bath that can control the temperature of 1 ° C so that the coating surface of the work cloth is on the hot water surface side and leave it for 20 minutes. In this case, the container is sealed with a container wall so that no outside air flows between the work cloth and the hot water. After standing for 20 minutes, the state of water droplets (condensation) on the surface of the coating layer was observed and classified as follows.
水滴が全面に付着している。(多) 水滴が約30%面状に付着している。(中) 水滴が点状にわずかに付着している。(少) 水滴は殆ど認められない。(なし) さらにこの時に加工面の水滴を濾紙にて軽く拭取り加
工布中に残存している水分を吸湿性として重量増加率
(%)で比較した。結果を第2表に示す。Water droplets adhere to the entire surface. (Many) Water droplets adhere to the surface approximately 30%. (Medium) Water droplets are slightly attached like dots. (Small) Water droplets are hardly observed. (None) Further, at this time, water drops on the processed surface were lightly wiped with a filter paper, and the moisture remaining in the processed cloth was compared with the weight increase rate (%) as hygroscopicity. The results are shown in Table 2.
実施例3及び4、比較例2 エステルトリコット(40デニール、ウェル50本/inc
h、コース55/inch)の通常染色布を実施例1と同様の撥
水剤にて撥水処理を施し、140℃で2分間乾燥、熱処理
した布帛を得た(第1層の形成)。次いで実施例1と同
じく透湿性防水層(第2層)を形成しその上にアクリル
樹脂の20%トルエン溶液(東亜ペイント社製:トアクロ
ンXE−2511=80部、透湿性一液ウレタンの25%トルエン
/イソプロピールアルコール溶液(大日精化工業社製:
ハイムレンNPU−5)20部、トルエン20部、イソシアネ
ート化合物(前掲)3部、カルボキシルメチルキチン
(片倉チッカリン社製:CMキチン)の0.5%水溶液20部の
混合調製液を湿潤状態で100g/m2になるようにリバース
ロールコーターにて塗布し70℃で2分間オーブン中にて
乾燥し乾燥状態で18g/m2の吸水性を有する透湿性多孔質
≠キチン膜層を形成した(第3層の形成)。その後更に
布帛を樹脂との接着性をより高めるために120℃で2分
間仕上げセットを行った。Examples 3 and 4, Comparative Example 2 Ester tricot (40 denier, 50 wells / inc
h, course 55 / inch) was treated with the same water-repellent agent as in Example 1, dried at 140 ° C. for 2 minutes, and heat-treated to obtain a fabric (first layer formation). Next, a moisture-permeable waterproof layer (second layer) was formed in the same manner as in Example 1, and a 20% toluene solution of an acrylic resin (manufactured by Toa Paint Co., Ltd .: Toaclon XE-2511 = 80 parts, 25% of a moisture-permeable one-liquid urethane) was formed thereon. Toluene / isopropyl alcohol solution (Dainichi Seika Kogyo Co., Ltd .:
Haimuren NPU-5) 20 parts, 20 parts of toluene, the isocyanate compound (supra), 3 parts of carboxymethyl chitin (Katakura Chikkarin Co., Ltd. in the wet state a mixed preparation of a 0.5% aqueous solution 20 parts of CM chitin) 100 g / m 2 And dried in an oven at 70 ° C. for 2 minutes to form a moisture-permeable porous し -chitin film layer having a water absorption of 18 g / m 2 in a dry state (the third layer). Formation). Thereafter, the fabric was further set at 120 ° C. for 2 minutes in order to further enhance the adhesion to the resin.
本発明中の布帛に対するキチン量は実施例3では0.5
%、実施例4の布帛では1.0%、比較例2の布帛では実
施例7と同様の方法にて0.3%含有量のものを作成し
た。これらは脱アセチル化キチン水溶液の量を変更して
得た。In Example 3, the amount of chitin relative to the fabric in the present invention was 0.5
%, 1.0% for the fabric of Example 4, and 0.3% for the fabric of Comparative Example 2 in the same manner as in Example 7. These were obtained by changing the amount of the aqueous solution of deacetylated chitin.
実施例3及び4そして比較例2は実施例1と同じ方法
にて測定した。結果を第2表に示す。Examples 3 and 4 and Comparative Example 2 were measured in the same manner as in Example 1. The results are shown in Table 2.
比較例3及び4 比較例3は、参考例3と同様の処理剤にて撥水処理及
び実施例1と同様の熱処理を施した基布を用いた。 Comparative Examples 3 and 4 In Comparative Example 3, a base fabric subjected to a water-repellent treatment and a heat treatment similar to that of Example 1 using the same treatment agent as that of Reference Example 3 was used.
この布帛にジメチルホルムアミドに溶解されたポリウ
レタン樹脂液(20%溶液)100部に対し、溶剤型弗素系
撥水剤1部およびトリメチロールプロパン−ヘキサメチ
レンジイソシアネート(30%)1部を混合したコーティ
ング液を湿潤付着量で250g/m2となるようコーティング
を行い(第2層の形成)よく知られている湿式凝固法に
よって得た。また比較例4は実施例3において使用した
同じ前処理(第1層)を施したエステルトリコットに一
般のポリエチレングリコール等親水性グリコール類を含
んで合成された無孔タイプの透湿性ポリウレタン樹脂液
(固形分25%溶液)をリバースロールコート方式等で乾
燥状態で10〜12g/m2になるように塗布し乾燥して得られ
る透湿性防水布帛である。A coating solution obtained by mixing 1 part of a solvent-type fluorine-based water repellent and 1 part of trimethylolpropane-hexamethylene diisocyanate (30%) with 100 parts of a polyurethane resin liquid (20% solution) dissolved in dimethylformamide on the cloth. Was coated so as to have a wet adhesion amount of 250 g / m 2 (formation of a second layer) by a well-known wet coagulation method. In Comparative Example 4, a non-porous type moisture-permeable polyurethane resin liquid (Synthesis) containing hydrophilic glycols such as general polyethylene glycol in the ester tricot having been subjected to the same pretreatment (first layer) used in Example 3 was used. This is a moisture-permeable waterproof fabric obtained by applying a solution (solid content: 25%) in a dry state by a reverse roll coating method or the like so as to be 10 to 12 g / m 2 and drying.
得られた結果を比較例3は比較例3として第3表に示
す。The results are shown in Table 3 for Comparative Example 3 as Comparative Example 3.
第2表と3表より本発明による布帛は、従来の透湿防
水布よりすぐれた透湿性及び結露防止性そして吸湿性が
得られることが明らかである。 From Tables 2 and 3, it is clear that the fabrics according to the present invention have better moisture permeability, anti-condensation and moisture absorption than conventional moisture-permeable and waterproof fabrics.
実施例5 実施例1と同様の構成であるが、第3層はキチン系物
質を含まない樹脂層を形成させることが出来る。Example 5 The structure is the same as that of Example 1, but the third layer can be formed by a resin layer containing no chitin-based substance.
第3層に透湿性を付与することにより結露防止性及び
吸湿性が生じる。(第2図参照) 実施例6 実施例1と同様の構成であるが、第2層はキチン系物
質を含まない樹脂層を形成させることが出来る。By imparting moisture permeability to the third layer, dew condensation preventing properties and moisture absorbing properties are generated. Example 6 Example 6 has the same configuration as Example 1, but the second layer can be formed by a resin layer containing no chitin-based substance.
第3層によってより透湿性を高め第1層、第2層への
吸水性を向上させる。(第3図参照) 実施例7 基布上に直接キチン系物質を含んだ樹脂層を形成する
ことが出来る。しかしこの場合、基布の厚さ方向への樹
脂の浸透が大きくなると基布を通して樹脂溶液が基布の
裏面へ抜け出て、その結果風合硬化を起こしたり引裂強
度の低下をきたす。The third layer further increases the moisture permeability and improves the water absorption of the first and second layers. (See FIG. 3) Example 7 A resin layer containing a chitin-based substance can be directly formed on a base cloth. However, in this case, when the penetration of the resin in the thickness direction of the base cloth increases, the resin solution escapes to the back surface of the base cloth through the base cloth, and as a result, the hand hardens and the tear strength decreases.
実施例8 基布にあらかじめ撥水処理を施した後基布上にキチン
系物質を含んだ透湿樹脂層を形成することが出来る。こ
の場合、基布に撥水性が有る為実施例7の欠点をカバー
することが出来る。Example 8 A water-repellent treatment is applied to a base fabric in advance, and then a moisture-permeable resin layer containing a chitin-based substance can be formed on the base fabric. In this case, since the base fabric has water repellency, the drawback of Embodiment 7 can be covered.
実施例9 基布を参考例1に従ってキチン系物質を含んだ配合液
に含浸処理し、熱処理を施した後、その基布の片面に実
施例3と同様に透湿性合成樹脂層さらに、その上にキチ
ン系物質を含む多孔質ポリウレタン樹脂層を形成するこ
とが出来る。Example 9 A base fabric was impregnated with a liquid formulation containing a chitin-based substance according to Reference Example 1 and subjected to a heat treatment, and then, on one surface of the base fabric, as in Example 3, a moisture-permeable synthetic resin layer was further added. To form a porous polyurethane resin layer containing a chitin-based material.
実施例10 実施例9の多孔質ポリウレタン層の上に更にキチン系
物質を含む多孔質透湿ポリウレタン樹脂層を形成し、耐
摩耗性などの強力を向上させることが出来る。Example 10 A porous moisture-permeable polyurethane resin layer containing a chitin-based substance was further formed on the porous polyurethane layer of Example 9 to improve the strength such as abrasion resistance.
実施例11 離型紙上にキチン系物質を含む透湿性樹脂層を形成
し、更にその樹脂層の上に接着剤となる透湿性樹脂層を
形成しその上に基布を圧着して後離型紙より樹脂層を剥
離する、いわゆる転写コーティング方式によって作成す
ることが出来る。Example 11 A moisture-permeable resin layer containing a chitin-based substance was formed on release paper, a moisture-permeable resin layer serving as an adhesive was further formed on the resin layer, and a base cloth was pressed thereon to release the release paper. It can be formed by a so-called transfer coating method in which the resin layer is more peeled off.
本発明の透湿性防水布帛は、吸水性,水分の拡散性,
放出性、抗結露性が従来の透湿性防水布帛に比べて著し
く優れている。したがって、発汗および汗の蒸気は布帛
に吸収され、速やかに布帛から放出させることができ
る。The moisture-permeable waterproof fabric of the present invention has a water absorbing property, a water diffusing property,
The release property and the anti-condensation property are remarkably superior to those of the conventional moisture-permeable waterproof fabric. Therefore, the sweat and the vapor of the sweat are absorbed by the fabric and can be quickly released from the fabric.
さらにキチン系物質は優れた抗菌性を有するので、良
好な抗菌性を有する製品を本発明による布帛から作るこ
とができる。Furthermore, chitin-based substances have excellent antibacterial properties, so that products with good antibacterial properties can be made from the fabric according to the present invention.
本発明による布帛は例えばスキーウエア、ウインドブ
レーカー、などの防水衣料、オムツカバー、サニタリー
用途、スポーツウエアー、下着、寝具、さらに壁紙等建
材、靴のインナー材、スポーツ帽子等の広範囲な用途で
有用に用いることができる。The fabric according to the present invention is useful in a wide range of applications such as waterproof clothing such as ski wear, windbreakers, diaper covers, sanitary applications, sportswear, underwear, bedding, and other building materials such as wallpaper, inner materials for shoes, and sports hats. Can be used.
第1図〜第4図は本発明による基布と、基布の表面に順
次付与された少くとも2層の合成樹脂層から成り、該少
くとも2層の合成樹脂層内の少くとも1層にキチン系物
質が含有されている布帛の各種実施例を示す断面図であ
って、第1図は樹脂層が2層である場合の実施例の布帛
の断面図であり、第2図は樹脂層が3層であり、中間層
にキチン系物質が含まれている実施例の布帛の断面図で
あり、第3図は樹脂層が3層であり、外側層にキチン系
物質が含まれている実施例の布帛の断面図であり、第4
図は樹脂層が3層であり、中間層と外側層にキチン系物
質が含まれている実施例の布帛の断面図である。 1……基布、1a……経糸、 1b……緯糸、2……撥水剤を含んでいる部分、 3……透湿性を有する樹脂層、 4,5……キチン系物質と合成樹脂を含む層、 6……キチン系物質。1 to 4 show a base cloth according to the present invention and at least two synthetic resin layers sequentially applied to the surface of the base cloth, and at least one of the at least two synthetic resin layers. FIG. 1 is a cross-sectional view showing various examples of a cloth containing a chitin-based material in FIG. 1; FIG. 1 is a cross-sectional view of the cloth of the example in which the number of resin layers is two; FIG. FIG. 3 is a cross-sectional view of a fabric having three layers and an intermediate layer containing a chitin-based material, and FIG. 3 shows a three-layer resin layer and an outer layer containing a chitin-based material. FIG. 4 is a cross-sectional view of the fabric of
The figure is a cross-sectional view of the fabric of the embodiment in which there are three resin layers and the intermediate layer and the outer layer contain a chitin-based substance. DESCRIPTION OF SYMBOLS 1 ... Base fabric, 1a ... Warp, 1b ... Weft, 2 ... Part containing water repellent, 3 ... Resin layer having moisture permeability, 4, 5 ... Chitin-based material and synthetic resin Layer containing 6 ... Chitin-based substance.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 秋田 晃男 滋賀県草津市矢橋町23番地の28 (72)発明者 宇野 智久 滋賀県甲賀郡甲西町岩根499―127 (56)参考文献 特開 昭60−126386(JP,A) 特開 昭58−183169(JP,A) (58)調査した分野(Int.Cl.6,DB名) D06M 15/00 - 15/72──────────────────────────────────────────────────続 き Continuing from the front page (72) Inventor Akio Akita 23-28, Yabashi-cho, Kusatsu-shi, Shiga Prefecture (72) Inventor Tomohisa Uno 499-127 Iwane, Kosai-cho, Koga-gun, Shiga Pref. JP-A-58-183169 (JP, A) (58) Fields investigated (Int. Cl. 6 , DB name) D06M 15/00-15/72
Claims (1)
少なくとも2層からなる3000g/m2/24hours以上の透湿度
を有する防水性合成樹脂層からなり、かつ前記合成樹脂
層の少なくとも1層にキチン系物質が分散、含有されて
いる透湿性防水布帛。[1 claim: a base fabric, made of a waterproof synthetic resin layer having a 3000 g / m 2 / 24hours or more moisture permeability of at least two layers which are sequentially applied to the surface of the base fabric, and the synthetic resin layer A moisture-permeable waterproof fabric in which a chitin-based substance is dispersed and contained in at least one layer.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP26812789A JP2845517B2 (en) | 1988-10-17 | 1989-10-17 | Breathable waterproof fabric |
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP25940988 | 1988-10-17 | ||
| JP63-259409 | 1988-10-17 | ||
| JP10995989 | 1989-04-28 | ||
| JP1-109959 | 1989-04-28 | ||
| JP26812789A JP2845517B2 (en) | 1988-10-17 | 1989-10-17 | Breathable waterproof fabric |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0376871A JPH0376871A (en) | 1991-04-02 |
| JP2845517B2 true JP2845517B2 (en) | 1999-01-13 |
Family
ID=27311604
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP26812789A Expired - Lifetime JP2845517B2 (en) | 1988-10-17 | 1989-10-17 | Breathable waterproof fabric |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2845517B2 (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100473500B1 (en) * | 2002-09-24 | 2005-03-10 | 한국섬유개발연구원 | Method of producing for Water Vapor Permeable/Waterproof Finished textiles containing chitosan |
| JP4592459B2 (en) * | 2005-03-22 | 2010-12-01 | 学校法人 関西大学 | Antibacterial composition containing chitosan |
| CN103696257A (en) * | 2013-12-05 | 2014-04-02 | 吴江市亨德利纺织厂 | Production technology of water absorption breathable cloth |
| JP6577332B2 (en) * | 2015-10-29 | 2019-09-18 | 旭化成株式会社 | Antibacterial synthetic fiber fabric with excellent antibacterial performance |
| JP6636217B2 (en) * | 2017-11-16 | 2020-01-29 | 三菱電機株式会社 | Total heat exchange element and total heat exchanger |
-
1989
- 1989-10-17 JP JP26812789A patent/JP2845517B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0376871A (en) | 1991-04-02 |
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