KR101599399B1 - Green polyurethane skin material and a method of manufacturing - Google Patents
Green polyurethane skin material and a method of manufacturing Download PDFInfo
- Publication number
- KR101599399B1 KR101599399B1 KR1020150024962A KR20150024962A KR101599399B1 KR 101599399 B1 KR101599399 B1 KR 101599399B1 KR 1020150024962 A KR1020150024962 A KR 1020150024962A KR 20150024962 A KR20150024962 A KR 20150024962A KR 101599399 B1 KR101599399 B1 KR 101599399B1
- Authority
- KR
- South Korea
- Prior art keywords
- skin
- fabric
- polyurethane
- adhesive
- ethyl ketone
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 239000004814 polyurethane Substances 0.000 title claims abstract description 120
- 229920002635 polyurethane Polymers 0.000 title claims abstract description 119
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 22
- 239000000463 material Substances 0.000 title claims abstract description 19
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims abstract description 249
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims abstract description 199
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims abstract description 129
- 239000004744 fabric Substances 0.000 claims abstract description 118
- 239000000853 adhesive Substances 0.000 claims abstract description 78
- 230000001070 adhesive effect Effects 0.000 claims abstract description 76
- 239000005556 hormone Substances 0.000 claims abstract description 67
- 229940088597 hormone Drugs 0.000 claims abstract description 67
- 230000007613 environmental effect Effects 0.000 claims abstract description 63
- 238000000034 method Methods 0.000 claims abstract description 40
- 230000008569 process Effects 0.000 claims abstract description 33
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims abstract description 31
- 239000000126 substance Substances 0.000 claims abstract description 30
- 238000001035 drying Methods 0.000 claims abstract description 28
- 239000002904 solvent Substances 0.000 claims abstract description 24
- 239000003085 diluting agent Substances 0.000 claims abstract description 23
- 239000000203 mixture Substances 0.000 claims abstract description 21
- 230000032683 aging Effects 0.000 claims abstract description 20
- 238000007664 blowing Methods 0.000 claims abstract description 19
- 238000002156 mixing Methods 0.000 claims abstract description 18
- -1 polyethylene Polymers 0.000 claims abstract description 18
- 239000000049 pigment Substances 0.000 claims abstract description 17
- 239000002861 polymer material Substances 0.000 claims abstract description 17
- 239000012790 adhesive layer Substances 0.000 claims abstract description 16
- 238000013329 compounding Methods 0.000 claims abstract description 13
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims abstract description 12
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000004745 nonwoven fabric Substances 0.000 claims abstract description 11
- 238000005096 rolling process Methods 0.000 claims abstract description 11
- 239000004698 Polyethylene Substances 0.000 claims abstract description 10
- 229920000573 polyethylene Polymers 0.000 claims abstract description 10
- 238000003825 pressing Methods 0.000 claims abstract description 9
- 239000002759 woven fabric Substances 0.000 claims abstract description 9
- 150000001875 compounds Chemical class 0.000 claims abstract description 8
- 238000000465 moulding Methods 0.000 claims abstract description 7
- 229920000642 polymer Polymers 0.000 claims abstract description 7
- 238000009987 spinning Methods 0.000 claims abstract description 7
- 230000003647 oxidation Effects 0.000 claims abstract description 6
- 238000007254 oxidation reaction Methods 0.000 claims abstract description 6
- 229920002994 synthetic fiber Polymers 0.000 claims abstract description 6
- 239000012209 synthetic fiber Substances 0.000 claims abstract description 6
- 239000002994 raw material Substances 0.000 claims abstract description 5
- 239000012855 volatile organic compound Substances 0.000 claims abstract description 5
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 claims abstract description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 4
- 238000001704 evaporation Methods 0.000 claims abstract description 3
- 238000012216 screening Methods 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 3
- 238000010791 quenching Methods 0.000 claims 1
- 230000000171 quenching effect Effects 0.000 claims 1
- 238000007751 thermal spraying Methods 0.000 abstract description 2
- MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 abstract 3
- 239000004433 Thermoplastic polyurethane Substances 0.000 description 17
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 17
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 16
- 229920005862 polyol Polymers 0.000 description 16
- 150000003077 polyols Chemical class 0.000 description 16
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 15
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 10
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 9
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 8
- 239000000020 Nitrocellulose Substances 0.000 description 8
- FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 8
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 8
- 229920001220 nitrocellulos Polymers 0.000 description 8
- 229920005906 polyester polyol Polymers 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 229920002554 vinyl polymer Polymers 0.000 description 7
- 239000000178 monomer Substances 0.000 description 6
- 229920005830 Polyurethane Foam Polymers 0.000 description 5
- 229940093476 ethylene glycol Drugs 0.000 description 5
- 239000003960 organic solvent Substances 0.000 description 5
- 239000005022 packaging material Substances 0.000 description 5
- 239000011496 polyurethane foam Substances 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 5
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 4
- 239000005711 Benzoic acid Substances 0.000 description 4
- 239000004721 Polyphenylene oxide Substances 0.000 description 4
- 239000004743 Polypropylene Substances 0.000 description 4
- 239000004793 Polystyrene Substances 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 4
- 235000010233 benzoic acid Nutrition 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 229930003836 cresol Natural products 0.000 description 4
- 238000010520 demethylation reaction Methods 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 239000002649 leather substitute Substances 0.000 description 4
- 239000003607 modifier Substances 0.000 description 4
- 239000003495 polar organic solvent Substances 0.000 description 4
- 229920002239 polyacrylonitrile Polymers 0.000 description 4
- 229920000570 polyether Polymers 0.000 description 4
- 229920001155 polypropylene Polymers 0.000 description 4
- 229920002223 polystyrene Polymers 0.000 description 4
- 229920005749 polyurethane resin Polymers 0.000 description 4
- 239000004800 polyvinyl chloride Substances 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- 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 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 230000017858 demethylation Effects 0.000 description 3
- 125000000524 functional group Chemical group 0.000 description 3
- 238000009413 insulation Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 239000005056 polyisocyanate Substances 0.000 description 3
- 229920001228 polyisocyanate Polymers 0.000 description 3
- 229920000915 polyvinyl chloride Polymers 0.000 description 3
- 229920001169 thermoplastic Polymers 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 2
- 239000012963 UV stabilizer Substances 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000004566 building material Substances 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000004035 construction material Substances 0.000 description 2
- KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 description 2
- 125000005442 diisocyanate group Chemical group 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 210000004177 elastic tissue Anatomy 0.000 description 2
- 238000001523 electrospinning Methods 0.000 description 2
- PSLIMVZEAPALCD-UHFFFAOYSA-N ethanol;ethoxyethane Chemical compound CCO.CCOCC PSLIMVZEAPALCD-UHFFFAOYSA-N 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 229910001385 heavy metal Inorganic materials 0.000 description 2
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- TZIHFWKZFHZASV-UHFFFAOYSA-N methyl formate Chemical compound COC=O TZIHFWKZFHZASV-UHFFFAOYSA-N 0.000 description 2
- 238000005192 partition Methods 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 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 2
- 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 1
- 235000007173 Abies balsamea Nutrition 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 239000004857 Balsam Substances 0.000 description 1
- HIBWGGKDGCBPTA-UHFFFAOYSA-N C=CC1=CC=CC=C1.C=CC1=CC=CC=C1 Chemical compound C=CC1=CC=CC=C1.C=CC1=CC=CC=C1 HIBWGGKDGCBPTA-UHFFFAOYSA-N 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- 239000004970 Chain extender Substances 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000004609 Impact Modifier Substances 0.000 description 1
- 244000018716 Impatiens biflora Species 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- HCUQZYPFHWGZFD-UHFFFAOYSA-N butan-2-one;pentan-3-one Chemical compound CCC(C)=O.CCC(=O)CC HCUQZYPFHWGZFD-UHFFFAOYSA-N 0.000 description 1
- 150000001718 carbodiimides Chemical class 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- UXGNZZKBCMGWAZ-UHFFFAOYSA-N dimethylformamide dmf Chemical compound CN(C)C=O.CN(C)C=O UXGNZZKBCMGWAZ-UHFFFAOYSA-N 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 210000000750 endocrine system Anatomy 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 229920001002 functional polymer Polymers 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 150000002611 lead compounds Chemical class 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000002121 nanofiber Substances 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 239000008029 phthalate plasticizer Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 230000036314 physical performance Effects 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920006306 polyurethane fiber Polymers 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- 238000007142 ring opening reaction Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000011145 styrene acrylonitrile resin Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 150000003606 tin compounds Chemical class 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical group O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
- D06N3/12—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins
- D06N3/14—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins with polyurethanes
-
- 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
- D06M17/00—Producing multi-layer textile fabrics
- D06M17/04—Producing multi-layer textile fabrics by applying synthetic resins as adhesives
- D06M17/10—Polyurethanes polyurea
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
- D06N3/0056—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the compounding ingredients of the macro-molecular coating
- D06N3/0059—Organic ingredients with special effects, e.g. oil- or water-repellent, antimicrobial, flame-resistant, magnetic, bactericidal, odour-influencing agents; perfumes
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
- D06N3/0056—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the compounding ingredients of the macro-molecular coating
- D06N3/0065—Organic pigments, e.g. dyes, brighteners
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
- D06N3/007—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by mechanical or physical treatments
- D06N3/0077—Embossing; Pressing of the surface; Tumbling and crumbling; Cracking; Cooling; Heating, e.g. mirror finish
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N2211/00—Specially adapted uses
- D06N2211/12—Decorative or sun protection articles
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N2211/00—Specially adapted uses
- D06N2211/12—Decorative or sun protection articles
- D06N2211/14—Furniture, upholstery
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Dispersion Chemistry (AREA)
- Laminated Bodies (AREA)
Abstract
본 발명은 가구나 기타 인테리어 소재로 사용되는 인조피혁을 제조함에 있어서, 인체에 유해한 환경호로몬의 발생을 최소화한 친환경 폴리우레탄 스킨 원단 및 그 제조방법에 관한 것으로, 고분자 물질인 폴리우레탄(Poly Urethane)과, 고분자화합물인 용제(溶劑)로 합성섬유의 방사용제(紡絲溶劑)로 이용되는 다이메틸폼아마이드(D.M.F : Dimethyl Formamide)와, 부틸알코올의 산화로 얻어지고 용제로 쓰이는 메틸에틸케톤(M.E.K:methyl ethyl ketone)과, 안료를 배합하여 스킨(skin) 소재를 얻는 스킨배합공정과;
상기 고분자 물질인 폴리우레탄(Poly Urethane)과, 다이메틸폼아마이드(D.M.F : Dimethyl Formamide)와, 메틸에틸케톤(M.E.K:methyl ethyl ketone)과, 벤젠의 메틸 치환체로 쓰여지는 희석제인 톨루엔(Toluene)을 배합하여 접착제를 얻는 접착제 배합공정과;
종이에 폴리에틸렌(Poly Ethylene)을 코팅한 표면에 다양한 음각무늬를 형성한 이형지(Release Paper)를 선택하여 이형지 롤을 구비하는 이형지 선택공정과;
상기 이형지 선택공정에서 선택한 이형지의 다양한 음각무늬가 형성된 표면에 상기 스킨배합공정에서 얻어진 스킨을 균일하게 도포하는 스킨도포공정과;
상기 스킨도포공정에서 음각무늬가 형성된 표면에 도포하여 스킨을 형성한 상태에서 건조챔버에서 희석제인 다이메틸폼아마이드(D.M.F : Dimethyl Formamide)와, 메틸에틸케톤(M.E.K:methyl ethyl ketone)의 성분을 증발하여 날려보내고 안료를 배합하여 색상을 창출하는 고분자 물질인 폴리우레탄(Poly Urethane)만으로 건조성형된 스킨을 형성하는 스킨성형건조공정과;
상기 스킨성형건조공정에서 건조성형된 스킨의 표면에 상기 접착제 배합공정에서 얻어진 접착제를 도포하는 접착제도포공정과;
상기 접착제도포공정에서 스킨의 표면에 도포한 접착제를 120℃~130℃의 건조챔버에서 희석제인 다이메틸폼아마이드(D.M.F : Dimethyl Formamide)와, 메틸에틸케톤(M.E.K:methyl ethyl ketone)과, 희석제인 톨루엔(Toluene)의 성분을 증발하여 날려보내서 끈적끈적한 상태의 폴리우레탄(Poly Urethane)접착층을 형성하는 접착제건조공정과;
상기한 공정으로 다양한 음각무늬를 형성한 이형지(Release Paper)의 표면에 고분자 물질인 폴리우레탄(Poly Urethane)만으로 성형된 스킨을 형성하고, 상기 스킨의 표면에 형성한 끈적끈적한 상태의 폴리우레탄(Poly Urethane)접착층 위에 직포나 부직포로 된 원단을 덮어서 폴리우레탄 접착제가 상기 원단에 일체로 침투하여 접합하도록 압착롤러로 압착하는 원단전사공정과;
상기 원단전사공정에서 스킨의 표면에 형성한 폴리우레탄(Poly Urethane)접착층의 폴리우레탄 접착제가 상기 원단에 일체로 침투하여 스킨과 원단이 일체로 접합한 상태에서 롤 상태로 감아주는 원단롤링공정과;
상기 원단롤링공정에서 롤 상태로 감긴 상태에서 80℃~90℃로 유지하는 숙성챔버에서 12시간 숙성시켜서 잔여 다이메틸폼아마이드(D.M.F : Dimethyl Formamide)와, 메틸에틸케톤(M.E.K:methyl ethyl ketone)과, 희석제인 톨루엔(Toluene)의 성분을 완전히 증발하여 날려보내서 끈적끈적한 상태의 폴리우레탄(Poly Urethane)접착제를 경화시킴으로써 원단과 스킨이 일체가 되도록 접합숙성시키는 숙성공정과;
상기 숙성공정에서 접착제가 완전히 경화되어 원단과 스킨이 일체로 된 상태에서 이형지를 스킨의 표면에서 분리하는 이형지 분리공정;에,
원단과 스킨이 일체로 접합되어 롤 상태로 감긴 스킨 원단을 풀어서 180℃의 열간롤러나 열간챔버를 분당 10m 씩 통과시키면서 가열함과 동시에 간접열 분사식으로 열풍을 불어서 스킨 원단으로부터 추출되는 총 휘발성 유기화합물(TVOC), 톨루엔(Toluene), 포름알데히이드(Formaldehyde)를 포함한 유해물질인 환경호르몬을 환풍기로 불어내어 제거하는 환경호르몬 제거 공정과;
상기 환경호르몬 제거공정에서 환경호르몬이 제거된 스킨을 200℃의 간접열로 표면을 가열하고 180℃의 직접열로 이면을 가열한 다음 급랭하여 표면 조직이 조밀하게 재결정되어 스킨의 내부에 함유된 잔여 유해물질인 환경호르몬이 외부로 누출되지 않도록 처리하는 환경호르몬 차폐공정을 더 실시하여 이루어짐을 특징으로 하는 친환경 폴리우레탄 스킨 원단 제조방법.The present invention relates to an environmentally friendly polyurethane skin fabric which minimizes the generation of environmental hormones harmful to human body and a method of manufacturing the same, and more particularly to a polyurethane (polyurethane) Dimethyl formamide (DMF) used as a spinning solvent for synthetic fibers as a solvent which is a polymer compound, methyl ethyl ketone (MEK) obtained by oxidation of butyl alcohol and used as a solvent, methyl ethyl ketone) and a pigment to obtain a skin material;
The above polymer material, polyurethane, dimethyl formamide (DMF), methyl ethyl ketone (MEK), and toluene (Toluene), which is a diluent used as a methyl substituent of benzene, An adhesive compounding step of compounding the adhesive to obtain an adhesive;
A releasing paper selection step of selecting a release paper having various engraved patterns on a surface of polyethylene (Poly Ethylene) coated on a paper sheet to provide a releasing paper roll;
A skin applying step of uniformly applying the skins obtained in the skin mixing step to the surface of the release paper selected in the release paper selecting step;
(DMF) and methyl ethyl ketone (MEK: methyl ethyl ketone) are evaporated in a drying chamber in a state where the skin is formed by applying the composition on the engraved surface in the skin applying step, A skin forming drying step of forming a dry-formed skin with polyurethane (Poly Urethane), which is a polymer material that blows away and forms a color by blending pigments;
An adhesive applying step of applying the adhesive obtained in the adhesive compounding step to the surface of the skin that has been dry-molded in the skin molding and drying step;
The adhesive applied on the surface of the skin in the adhesive application step is coated with a diluent such as dimethyl formamide (DMF), methyl ethyl ketone (MEK) and methyl ethyl ketone (diluent) in a drying chamber at 120 ° C to 130 ° C, An adhesive drying step of evaporating a component of toluene and blowing it to form a sticky sticky polyurethane (Urethane) adhesive layer;
In the process described above, a skin formed of only polyurethane (Poly Urethane), which is a polymer material, is formed on the surface of a release paper on which various engraved patterns are formed, and the skin formed of a sticky polyurethane A cloth transferring step of covering a fabric made of a woven fabric or a nonwoven fabric on the adhesive layer, and pressing the same with a pressing roller so that the polyurethane adhesive penetrates and adheres integrally with the fabric;
A raw material rolling process in which a polyurethane adhesive of a polyurethane adhesive layer formed on the surface of the skin in the fabric transferring step is integrally infiltrated into the fabric so that the skin and the fabric are integrally joined and wound in a roll state;
After aging for 12 hours in an aging chamber maintained at 80 ° C to 90 ° C in a rolled state in the far-end rolling process, residual DMF (dimethyl formamide), methyl ethyl ketone (MEK) , Aging the components of the diluent toluene (Toluene) completely evaporated and blowing them to cure the sticky sticky polyurethane (Urethane) adhesive so that the fabric and the skin are integrated;
A release paper separating step of separating the release paper from the surface of the skin in a state where the adhesive is completely cured in the aging step and the fabric and the skin are integrated,
The fabric is rolled in a rolled state by unifying the fabric and the skin, and heated by passing hot rollers and hot chambers at 180 ° C for 10m / min. At the same time, hot air is blown by indirect thermal spraying method to remove total volatile organic compounds (EN) An environmental hormone removal process for removing environmental hormones, which are harmful substances including nitrogen oxides (TVOC), toluene (Toluene) and formaldehyde,
The surface of the skin from which the environmental hormone was removed in the environmental hormone removal step was heated by indirect heat at 200 ° C, heated by direct heat at 180 ° C, and then quenched to densely recrystallize the surface texture. Wherein an environmental hormone shielding step is further performed to prevent environmental hormones, which are harmful substances, from leaking to the outside.
Description
본 발명은 가구나 기타 인테리어 소재로 사용되는 인조피혁을 제조함에 있어서, 인체에 유해한 환경호로몬의 발생을 억제한 친환경 폴리우레탄 스킨 원단 및 그 제조방법에 관한 것으로 본인이 선 발명하여 특허받은 특허출원 제10-2014-0023231호에 대한 개량 발명이다. The present invention relates to an environmentally friendly polyurethane skin fabric which suppresses the generation of harmful environmental hormones in the manufacture of artificial leather used as furniture and other interior materials, and a manufacturing method thereof, -2014-0023231.
현대 과학 문명의 발달에 따라 기능성 고분자가 개발되고 이에 폴리우레탄을 이용하여 인조피혁을 개발하여 그 사용용도를 점차 늘리고 있는 실정이다.Functional polymers have been developed according to the development of modern scientific civilization, and artificial leather is developed by using polyurethane, and the use thereof is gradually increasing.
종래에는 폴리우레탄의 경화 촉진제로 납 화합물(Pb-Octoates,Pb-Naphthanates)이나 주석화합물을 많이 사용하였는바, 이들 경화 촉진제는 상온에서도 주제인 우레탄 프리폴리머와 폴리올 경화제 혼합물을 용이하게 우레탄 반응을 시켜 우수한 물리적 성능을 부여하는 역할과 함께 가격 또한 상대적 경제성이 좋은 장점이 있는 반면, 다양한 질병을 유발하는 환경호르몬제이므로 사용에 많은 문제를 야기 시킨다.Conventionally, a large amount of lead compounds (Pb-Octoates, Pb-Naphthanates) or tin compounds have been used as a curing accelerator for polyurethane. These curing accelerators can easily react with a urethane prepolymer and a polyol curing agent mixture, In addition to providing physical performance, the price is also relatively economical, while the environmental hormones that cause various diseases cause problems in use.
그러나 카페트 및 기타 직물을 제조하는데 있어서 폴리우레탄을 도포하여 함유시키는 배면처리를 함으로써 직물에 벌크성과 강성을 주고, 파일섬유를 직물의 제 1 배면에 고착시키며 직물의 치수 안정성을 증가시키는 등 그 이용량이 점차 늘어나고 있는 실정이다.However, the use of backing to apply and contain polyurethane in the manufacture of carpets and other fabrics gives bulk and stiffness to the fabric, secures the pile fibers to the first backside of the fabric, and increases the dimensional stability of the fabric, It is gradually increasing.
이러한 폴리우레탄 배면물질의 사용은, 젠킨스(Jenkines)등의 미합중국 특허 제4,296,159호에 기술되어 있다.The use of such polyurethane backing materials is described in U.S. Patent No. 4,296,159 to Jenkines et al.
직물의 배면처리에 사용되는 폴리우레탄-형성 조성물의 조성은 다음의 4가지 경쟁적 요소에 의해결정된다. The composition of the polyurethane-forming composition used in the backside treatment of fabrics is determined by the following four competitive factors:
첫째로 배면처리된 직물은 주름이 잡히거나 시간이 경과함에 따라 변형되는 경향이 최소이어야 하고, 둘째로 저장 및 사용시 직물이 그 자체 또는 다른 물질에 붙지 않도록 배면은 가능한한 점성(tack)이 없어야 하며, 셋째로 배면은 기재 직물에 강하게 접착되어야 하며, 넷째로 환경호르몬의 발생을 최소화하여야 한다.The first backed fabric must be at least as prone to wrinkling or deformation as time elapses and secondly the backing should be as tack free as possible so that the fabric does not adhere to itself or to other materials during storage and use Third, the back side should be strongly adhered to the substrate fabric, and fourth, the occurrence of environmental hormones should be minimized.
열가소성 폴리우레탄(thermoplastic polyurethane: TPU)은 분자 내 우레탄 결합(-NHCOO-)의 반복단위를 가지는 중합체로서, 가열에 의하여 소성을 가지는 열가소성 플라스틱이고, 상온에서 고무와 같은 탄성을 가지는 탄성 중합체이다.Thermoplastic polyurethane (TPU) is a thermoplastic polymer having repeating units of urethane bonds in the molecule (-NHCOO-), and is a thermoplastic plastic having firing by heating, and is an elastic polymer having rubber-like elasticity at room temperature.
열가소성 폴리우레탄은 탄성력, 기계 물성, 진동 흡수성, 내마모성, 인열 강도, 내유성, 저온 특성 등이 우수하여 자동차 범퍼, 케이블 자켓, 합성 피혁 등에 널리 사용되고 있다. Thermoplastic polyurethanes are widely used in automobile bumpers, cable jackets, synthetic leather, etc. because of their excellent elasticity, mechanical properties, vibration absorbability, abrasion resistance, tear strength, oil resistance and low temperature characteristics.
열가소성 폴리우레탄은 배치식 또는 연속식 중합공정으로 제조될 수 있고, 산업적으로는 연속식 압출방법으로 많이 제조되고 있으며, 상기 방법은 출발 물질을 스크류 반응기에 계량 투입하고 축합반응을 수행한 후 균일한 과립형으로 전환시키는 방법이다(미국특허제3,642,964호).Thermoplastic polyurethanes can be prepared by batch or continuous polymerization processes and are industrially produced in a continuous extrusion process wherein the starting materials are metered into a screw reactor and subjected to a condensation reaction, (US Patent No. 3,642,964).
폴리우레탄은 통상 경질 세그먼트와 연질 세그먼트로 구성되며, 경질 세그먼트(hard segment)로는 방향족 디이소시아네이트로써 가장 대표적으로 많이 사용되는 톨루엔 디이소시아네이트(toluene diisocyanate;TDI), 디페닐메탄 디이소시아네이트(4,4`-diphenylmethane MDI)등이 있으며, 지방족 디이소시아네이트로는 헥사메틸렌 디이소시아네이트(hexamethylene diisocyanate; HDI), Hydrogenated MDI(H12MDI) 등이 사용되며, 기타 카보디이미드(carbodiimide)MDI등과 같은 변성MDI(modified MDI)와 스티렌(styrene) 혹은 SAN(styreneacrylonitrile)분산된 polymer polyol등이 제품으로 많이 나와 있다. The polyurethane is generally composed of a hard segment and a soft segment, and as a hard segment, toluene diisocyanate (TDI), diphenylmethane diisocyanate (4, 4 ') which are most commonly used as aromatic diisocyanates, hexamethylene diisocyanate (HDI), and hydrogenated MDI (H12MDI) are used as the aliphatic diisocyanate, and modified MDI such as carbodiimide MDI and the like are used as the aliphatic diisocyanate, And styrene (styrene) or styrene acrylonitrile (SAN) dispersed polymer polyol.
연질 세그먼트(soft segment)로는 폴리올을 사용하는데 폴리에스터 폴리올과 폴리에테르 폴리올이 있으며, 열가소성폴리우레탄에 사용되는 폴리올의 분자량은 대부분 1000~3000(g/mol)이고, 폴리에스터 폴리올은 아디핀산(adipic acid)과 에틸렌글리콜(ethyleneglycol;EG),디에틸렌글리콜(diethyleneglycol;DEG), 1,4-부틸렌글리콜 (butyleneglycol;BD) 등과 150℃이상에서 축합반응으로 제조되거나 카프로락톤(caprolactone) 개환(ring opening) 반응으로 제조된다. The soft segments include polyester polyols and polyether polyols. Polyols used in thermoplastic polyurethanes have a molecular weight of 1000 to 3000 (g / mol). Polyester polyols are adipic acid (ethylene glycol), ethyleneglycol (EG), diethyleneglycol (DEG), 1,4-butylene glycol (BD) and the like at a temperature of 150 ° C or higher, or by caprolactone ring opening opening reaction.
열가소성 폴리우레탄 제조시 대부분 폴리에스터 폴리올을 사용하며 내마모성, 기계강도 등이 우수하나, 내수성, 내알카리성 등이 취약하다. Polyester polyol is mostly used in the production of thermoplastic polyurethane. It has excellent abrasion resistance and mechanical strength, but it is weak in water resistance and alkali resistance.
폴리에테르 폴리올은 에틸렌옥사이드, 프로필렌옥사이드와 에틸렌글리콜, 글리세롤과 함께 수산화칼륨(KOH) 촉매 등을 사용하여 고압, 저온 반응으로 제조한다.The polyether polyol is prepared by a high-pressure, low-temperature reaction using ethylene oxide, propylene oxide, ethylene glycol, and glycerol together with a potassium hydroxide (KOH) catalyst.
폴리에테르 폴리올은 유연성(flexibility), 탄성력, 영구 압축 변형 등이 우수하므로 대부분 폴리우레탄 폼으로 제조되며, 제조된 폴리우레탄 폼은 자동차 시트(seat), 냉장고 단열재, 컨테이너 단열재, 건축 보온재 등에 널리 사용된다.Polyether polyols are mostly made of polyurethane foam because they have excellent flexibility, elasticity, and compression set. The polyurethane foam is widely used for automobile seat, refrigerator insulation, container insulation, building insulation, etc. .
최근 염화비닐계수지(polyvinyl chloride; PVC)의 연소시 발생하는 환경호르몬과 이에 따른 환경 규제 때문에 친환경 대체재로써 열가소성 폴리우레탄이 주목받고 있으며, PVC는 가소성과 내구성 등을 향상시키기 위한 첨가제로 열안정제, 활제, 가소제, UV안정제 등의 첨가제를 혼합한다. In recent years, thermoplastic polyurethane has been attracting attention as an eco-friendly substitute for environmental hormones generated by combustion of polyvinyl chloride (PVC) and environmental regulations. PVC is an additive for improving plasticity and durability, Additives such as lubricants, plasticizers, UV stabilizers and the like are mixed.
그러나 첨가제 중에서 가소제로 주로 사용되고 있는 프탈레이트계 가소제는 인체 내에서 내분비계를 교란시키는 소위 환경호르몬 물질로 알려져 있어서 그 사용이 제한되고 있다. However, phthalate plasticizer, which is mainly used as a plasticizer among additives, is known as a so-called environmental hormone substance which disturbs the endocrine system in the human body and its use is limited.
또한 납계, 주석 계통의 안정제나 UV안정제, 산화방지제로 사용되는 물질 역시 대부분 인체에 해로운 중금속이나 환경호르몬 물질에 해당하므로 대체재 개발이 시급히 요청되고 있는 실정이다. In addition, lead, tin-based stabilizers, UV stabilizers, and antioxidants are also used as heavy metals and environmental hormones, which are harmful to the human body.
자동차계기판(instrumental panel), door trim panel, headlining 등의 표피제로써 PVC 혹은 PVC/ABS alloy가 압출 시트(sheet)나 카렌다 가공 시트(sheet)가 널리 사용되고 있으며, 최근 환경적 문제로 이를 열가소성 폴리우레탄으로 대체하는 특허들이 많이 나와 있다. Extruded sheets or calendared sheets of PVC or PVC / ABS alloy are widely used as a skin agent for instrument panels, door trim panels, and headlining. Recently, as environmental problems, they have been used as thermoplastic polyurethane There are a lot of patents that replace it with.
이러한 용도 확대에도 불구하고 폴리우레탄은 분자 간 응집에너지(cohesive energy)와 극성이 높고 점착성이 강한 성질을 지니고 있어서 가공성과 생산성이 낮다는 문제점과, 열가소성 폴리우레탄은 방향족 디이소시아네트와 폴리에스터폴리올을 주로 사용하고 있기 때문에 가공성과 더불어 내후성(UV), 내열성, 내수성이 취약하다는 문제가 있다.In spite of this expansion of application, polyurethane has high cohesive energy, high polarity and high tackiness properties, which leads to low processability and productivity, and thermoplastic polyurethane has a problem of aromatic diisocyanate and polyester polyol There is a problem that it is poor in weatherability (UV), heat resistance, and water resistance in addition to processability because it is mainly used.
이에 지금까지 개발된 폴리우레탄에 대한 선행기술 특허문헌을 살펴보면 다음과 같다.The prior art patent literature on polyurethanes developed so far is as follows.
본 발명은 상기한 지금까지의 인조피혁을 비롯한 폴리우레탄 섬유에서 환경호르몬이나 기타 인체에 유해물질이 많이 검출되어 사용자의 건강을 위협하였는바, 이와 같은 문제점을 해결하여 인체에 유해한 환경호르몬의 발생을 억제하는 등 친환경적인 인체에 무해한 폴리우레탄 스킨 원단을 생산 공급함으로써 소비자를 보호하기 위하여 본인이 선 발명하여 특허받은 특허출원 제10-2014-0023231호에서 일부 미진한 사항을 개량하여 보다 완벽한 효과를 창출하도록 한 친환경 폴리우레탄 스킨 원단 및 그 제조방법을 실시함에 그 목적을 둔 것이다. The present invention solves the above-mentioned problems of the prior art polyurethane fibers, including artificial leather, by detecting a large amount of environmental hormones and other harmful substances in the human body, thereby threatening the health of the user. In order to protect the consumers by producing and supplying environmentally friendly polyurethane skin fabrics harmless to the human body, we have made some improvements in the patent application No. 10-2014-0023231, Friendly polyurethane skin fabric and a manufacturing method thereof.
상기한 목적을 달성하기 위한 본 발명은, 본인이 선 발명하여 특허받은 특허출원 제10-2014-0023231호인, 폴리에틸렌, 폴리스티렌, 폴리프로필렌 등의 석유화학 제품으로부터 얻어지고, 인체에 무해하며 우수한 탄성과 강도를 가지므로 건축자재, 포장재, 생활 소품 등으로 광범위하게 사용되는 고분자 물질인 폴리우레탄(Poly Urethane) 15~25중량%와, 극성 유기용매의 하나로 각종 화학반응의 용매로 이용되며, 특히 고분자화합물인 폴리아크릴로나이트릴의 뛰어난 용제(溶劑)로 합성섬유의 방사용제(紡絲溶劑)로 이용되는 다이메틸폼아마이드(D.M.F : Dimethyl Formamide) 20~30중량%와, 부틸알코올의 산화로 얻어지고 니트로셀룰로오스, 비닐 수지, 질산셀룰로오스 등의 용제로 쓰이는 메틸에틸케톤(M.E.K:methyl ethyl ketone) 45~55중량%와, 색상을 창출하기 위한 안료 2~8중량%를 배합하여 스킨(skin) 소재를 얻는 스킨배합공정과;In order to achieve the above object, the present invention relates to a method for producing a polyurethane foam, which is obtained from petroleum chemical products such as polyethylene, polystyrene and polypropylene, which is a patent application No. 10-2014-0023231 filed by the inventor of the present invention, 15 to 25% by weight of polyurethane (Poly Urethane), which is a polymer substance widely used for construction materials, packaging materials, and household accessories, and polar organic solvent, and is used as a solvent for various chemical reactions. Particularly, 20 to 30% by weight of dimethylformamide (DMF) used as a spinning solvent for synthetic fibers as an excellent solvent for polyacrylonitrile which is obtained by the oxidation of butyl alcohol 45 to 55% by weight of methyl ethyl ketone (MEK: methyl ethyl ketone) used as a solvent for nitrocellulose, vinyl resin and cellulose nitrate, and 2 to 8% by weight of pigment for producing color To obtain a skin material;
상기 고분자 물질인 폴리우레탄(Poly Urethane) 55~55중량%와, 다이메틸폼아마이드(D.M.F : Dimethyl Formamide) 5~15중량%와, 메틸에틸케톤(M.E.K:methyl ethyl ketone) 5~15중량%와, 벤젠의 메틸 치환체로 물에는 녹지 않지만 에탄올에테르벤젠 등 대부분의 유기 용매와는 혼합되고 용제용 외에 크레졸, 벤조산 등의 합성에 사용되며 탈메틸 반응에 의한 벤젠 제조에 쓰여지는 희석제인 톨루엔(Toluene) 25~35중량%을 배합하여 접착제를 얻는 접착제 배합공정과;The polymer material is prepared by mixing 55 to 55% by weight of polyurethane, 5 to 15% by weight of dimethylformamide (DMF), 5 to 15% by weight of methyl ethyl ketone (MEK) , Methyl substituent of benzene which is insoluble in water but is mixed with most organic solvents such as ethanol ether benzene, toluene (toluene) which is used for synthesis of cresol and benzoic acid besides for solvent, and diluent used for benzene production by demethylation, 25 to 35% by weight of the adhesive agent to obtain an adhesive agent;
종이에 폴리에틸렌(Poly Ethylene)을 코팅한 표면에 다양한 음각무늬를 형성한 이형지(Release Paper)를 선택하여 이형지 롤을 구비하는 이형지 선택공정과;A releasing paper selection step of selecting a release paper having various engraved patterns on a surface of polyethylene (Poly Ethylene) coated on a paper sheet to provide a releasing paper roll;
상기 이형지 선택공정에서 선택한 이형지의 다양한 음각무늬가 형성된 표면에 상기 스킨배합공정에서 얻어진 스킨을 0.1~0.3mm두께로 균일하게 도포하는 스킨도포공정과;A skin applying step of uniformly applying the skin obtained in the skin mixing step to a surface of 0.1 to 0.3 mm thickness uniformly on the surface of the release paper selected in the release paper selection step on the various engraved patterns;
상기 스킨도포공정에서 음각무늬가 형성된 표면에 도포하여 스킨을 형성한 상태에서 110℃~120℃의 건조챔버에서 희석제인 다이메틸폼아마이드(D.M.F : Dimethyl Formamide)와, 메틸에틸케톤(M.E.K:methyl ethyl ketone)의 성분을 증발하여 날려보내고 안료를 배합하여 색상을 창출하는 고분자 물질인 폴리우레탄(Poly Urethane)만으로 건조성형된 스킨을 형성하는 스킨성형건조공정과;In the skin applying step, the skin is applied to the surface having the engraved pattern, and in the drying chamber of 110 ° C to 120 ° C, dimethyl formamide (DMF: Dimethyl Formamide) and methyl ethyl ketone (MEK: methyl ethyl a skin forming drying step of forming a dry molded skin with polyurethane (polyurethane), which is a polymer material that evaporates and blows off the ingredients of the ketone and blends the pigment to form a color;
상기 스킨성형건조공정에서 건조성형된 스킨의 표면에 상기 접착제 배합공정에서 얻어진 접착제를 0.1~0.3mm 두께로 균일하게 도포하는 접착제도포공정과;An adhesive applying step of uniformly applying the adhesive obtained in the adhesive compounding step to the surface of the skin that has been dry-molded in the skin molding and drying step to a thickness of 0.1 to 0.3 mm;
상기 접착제도포공정에서 스킨의 표면에 도포한 접착제를 120℃~130℃의 건조챔버에서 희석제인 다이메틸폼아마이드(D.M.F : Dimethyl Formamide)와, 메틸에틸케톤(M.E.K:methyl ethyl ketone)과, 희석제인 톨루엔(Toluene)의 성분을 증발하여 날려보내서 끈적끈적한 상태의 폴리우레탄(Poly Urethane)접착층을 형성하는 접착제건조공정과;The adhesive applied on the surface of the skin in the adhesive application step is coated with a diluent such as dimethyl formamide (DMF), methyl ethyl ketone (MEK) and methyl ethyl ketone (diluent) in a drying chamber at 120 ° C to 130 ° C, An adhesive drying step of evaporating a component of toluene and blowing it to form a sticky sticky polyurethane (Urethane) adhesive layer;
상기한 공정으로 다양한 음각무늬를 형성한 이형지(Release Paper)의 표면에 고분자 물질인 폴리우레탄(Poly Urethane)만으로 성형된 스킨을 형성하고, 상기 스킨의 표면에 형성한 끈적끈적한 상태의 폴리우레탄(Poly Urethane) 접착층 위에 직포나 부직포로 된 원단을 덮어서 폴리우레탄 접착제가 상기 원단에 일체로 침투하여 접합하도록 압착롤러로 압착하는 원단전사공정과;In the process described above, a skin formed of only polyurethane (Poly Urethane), which is a polymer material, is formed on the surface of a release paper on which various engraved patterns are formed, and the skin formed of a sticky polyurethane A cloth transferring step of covering a fabric made of a woven fabric or a nonwoven fabric on the adhesive layer, and pressing the same with a pressing roller so that the polyurethane adhesive penetrates and adheres integrally with the fabric;
상기 원단전사공정에서 스킨의 표면에 형성한 폴리우레탄(Poly Urethane)접착층의 폴리우레탄 접착제가 상기 원단에 일체로 침투하여 스킨과 원단이 일체로 접합한 상태에서 롤 상태로 감아주는 원단롤링공정과;A raw material rolling process in which a polyurethane adhesive of a polyurethane adhesive layer formed on the surface of the skin in the fabric transferring step is integrally infiltrated into the fabric so that the skin and the fabric are integrally joined and wound in a roll state;
상기 원단롤링공정에서 롤 상태로 감긴 상태에서 80℃~90℃로 유지하는 숙성챔버에서 12시간 숙성시켜서 잔여 다이메틸폼아마이드(D.M.F : Dimethyl Formamide)와, 메틸에틸케톤(M.E.K:methyl ethyl ketone)과, 희석제인 톨루엔(Toluene)의 성분을 완전히 증발하여 날려보내서 끈적끈적한 상태의 폴리우레탄(Poly Urethane) 접착제를 경화시킴으로써 원단과 스킨이 일체가 되도록 접합숙성시키는 숙성공정과;After aging for 12 hours in an aging chamber maintained at 80 ° C to 90 ° C in a rolled state in the far-end rolling process, residual DMF (dimethyl formamide), methyl ethyl ketone (MEK) , Aging the components of the diluent toluene (Toluene) completely evaporated and blowing them to cure the sticky sticky polyurethane (Urethane) adhesive so that the fabric and the skin are integrated;
상기 숙성공정에서 접착제가 완전히 경화되어 원단과 스킨이 일체로 된 상태에서 이형지를 스킨의 표면에서 분리하는 이형지 분리공정;에 A release paper separating step of separating the release paper from the surface of the skin in a state where the adhesive is fully cured in the aging step and the fabric and the skin are integrated;
원단과 스킨이 일체 접합되어 롤 상태로 감긴 스킨 원단을 풀어서 180℃의 열간롤러나 열간챔버를 분당 10m 씩 통과시키면서 가열한 다음, 스킨 원단에 직접열풍을 불어서 스킨 원단으로부터 추출되는 총 휘발성 유기화합물(TVOC), 톨루엔(Toluene), 포름알데히이드(Formaldehyde)를 포함한 유해물질인 환경호르몬을 환풍기로 불어내어 제거하는 환경호르몬 제거 공정과;The fabric is rolled in a rolled state by unifying the fabric and the skin, and heated by passing hot rollers or hot chambers at 180 ° C for 10 m / min. Then, hot air is directly blown to the skin fabric to remove total volatile organic compounds An environmental hormone removing step of blowing out environmental hormones, which are toxic substances including benzene, toluene, formaldehyde, into a ventilator;
상기 환경호르몬 차폐공정은, 환경호르몬 제거공정에서 환경호르몬이 제거된 스킨 원단을 200℃의 간접열로 표면을 가열하고 180℃의 직접열로 이면을 가열한 다음 급랭하여 표면 조직이 조밀하게 재결정되어 스킨 원단의 내부에 함유된 잔여 유해물질인 환경호르몬이 외부로 누출되지 않도록 차폐처리하는 환경호르몬 차폐공정을; 더 실시하는 방법으로 직포나 부직포로 된 원단에 0.1~0.3mm 두께의 스킨이 일체로 접합되어 유해물질인 환경호로몬이 제거되고 난 잔여 유해물질인 환경호르몬이 누출되지 않도록 표면 조직이 조밀하게 구성한 친환경 폴리우레탄 스킨 원단을 구성한다. In the environmental hormone screening process, the surface of the skin, from which the environmental hormone is removed in the environmental hormone removing process, is heated by indirect heat at 200 ° C, the rear surface is heated by direct heat at 180 ° C and then quenched to densely recrystallize the surface texture An environmental hormone shielding process which shields the environmental hormone, which is a residual harmful substance contained in the skin fabric, from leaking to the outside; In addition, a 0.1-0.3 mm thick skin is bonded to a fabric made of woven fabric or nonwoven fabric in an integrated manner so that the environment hormone, which is a harmful substance, is removed, and the environment hormone, which is a harmful substance, It constitutes polyurethane skin fabric.
본 발명에 따른 친환경 폴리우레탄 바인더 조성물은 환경호르몬 규제 물질인 중금속을 포함하지 않았고, 희석제를 완전히 날려보내 유해물질의 잔류를 최소화함은 물론, 잔여 유해물질인 환경호르몬의 누출을 차단하여 사용중 잔여 유해물질인 환경호르몬이 배출되지 않아서 소비자를 보호하는 등 친환경적이면서도 각종 물리적 성질이 우수하다.The environmentally friendly polyurethane binder composition according to the present invention does not contain a heavy metal which is an environmental hormone regulating material and completely discharges the diluent to minimize the residual of harmful substances and also prevents leakage of the environment hormone which is a residual harmful substance, It is eco-friendly and has various physical properties such as protecting consumers because environmental hormones are not emitted.
도1은 본 발명을 실시하는데 따른 공정예시도.BRIEF DESCRIPTION OF THE DRAWINGS FIG.
먼저 본 발명의 실시예를 설명하기에 앞서 본 발명을 이루는 주요 물성에 대하여 알아보면 다음과 같다.Before describing the embodiments of the present invention, the main properties of the present invention will be described as follows.
폴리우레탄(PU: Poly Urethane): 폴리에틸렌, 폴리스티렌, 폴리프로필렌 등의 석유화학 제품으로부터 얻어지고, 인체에 무해하며 우수한 탄성과 강도를 가지므로 건축자재, 포장재, 생활 소품 등에 광범위하게 사용되는 고분자 물질이다.Polyurethane (PU): It is a polymer material which is obtained from petrochemical products such as polyethylene, polystyrene and polypropylene, is harmless to human body and has excellent elasticity and strength and is widely used for building materials, packaging materials, .
다이메틸폼아마이드(D.M.F : Dimethyl Formamide): 극성 유기용매의 하나로 각종 화학반응의 용매로 이용되며, 특히 고분자화합물인 폴리아크릴로나이트릴의 뛰어난 용제(溶劑)로 합성섬유의 방사용제(紡絲溶劑)로 이용되는 것으로, 화학식 C3H7NO이며, 무색 액체로 녹는점 61℃, 끓는점 153℃, 분자량 73.1로, 순수한 것은 냄새가 없지만 품질이 떨어지는 것은 다이메틸아민의 불순물 때문에 종종 비린내가 나며, 물과 유기 액체 대부분과 섞일 수 있고, 폼산메틸과 다이메틸아민으로 합성하거나 다이메틸아민과 일산화탄소의 반응으로 합성하며, 강한 산과 강한 염기에서 안정하지 않으며 특히 높은 온도에서 폼산과 다이메틸아민으로 가수분해된다.Dimethylformamide (DMF): As a polar organic solvent, it is used as a solvent for various chemical reactions. Particularly, it is an excellent solvent for polyacrylonitrile which is a polymer compound. It is a spinning solvent for synthetic fibers ), Which has the formula C3H7NO and has a melting point of 61 ° C, a boiling point of 153 ° C and a molecular weight of 73.1, which is a colorless liquid. Pure odorless but poor quality is often fishy due to impurities of dimethylamine, It can be mixed with most, synthesized by methyl formate and dimethylamine, or by the reaction of dimethylamine with carbon monoxide, which is not stable in strong acids and strong bases, especially hydrolysis with formic acid and dimethylamine at high temperatures.
메틸에틸케톤(M.E.K:methyl ethyl ketone): 니트로셀룰로오스, 비닐 수지, 질산셀룰로오스 등의 용제로써, 화학식 CH3COC2H5인, 방향이 있는 액체로서 끓는점 79.6℃이고, 부틸알코올의 산화로 얻어진다. Methyl ethyl ketone (M.E.K): A solvent such as nitrocellulose, vinyl resin or cellulose nitrate, which has a boiling point of 79.6 ° C as a liquid having the formula CH 3 COC 2 H 5 and is obtained by oxidation of butyl alcohol.
톨루엔(Toluene): 접착제에 사용되는 희석제로, 1835년 천연 수지인 톨루발삼(Tolu balsam)에서 처음으로 얻었기 때문에 톨루엔이라는 이름이 붙었고, 후에 석탄의 건류(乾溜)생성물 속에도 함유되어 있다는 것을 알고 석탄을 건류하여 얻은 경유를 황산으로 씻은 다음 정류(精溜)하여 만들게 된 벤젠의 메틸 치환체이며, 분자식은 C6H5CH3이고, 특이한 냄새가 나는 무색 액체이며, 분자량 92.14, 녹는점 95℃, 끓는점 110.8℃, 비중 0.87(15)로서, 물에는 녹지 않지만 에탄올에테르벤젠 등 대부분의 유기 용매와는 임의의 비율로 혼합하며, 용제용 외에 크레졸, 벤조산 등의 합성에 사용되며 탈메틸 반응에 의한 벤젠 제조에 쓰여진다.Toluene: A diluent used in adhesives. It was first named in toluene balsam, a natural resin, in 1835, so it was named toluene and was later found in the dry distillation of coal. Is a colorless liquid with a specific odor and has a molecular weight of 92.14, a melting point of 95 占 폚, a boiling point of 110.8 占 폚, a specific gravity 0.87 (15), which does not dissolve in water but is mixed with most organic solvents such as ethanol ether benzene at an arbitrary ratio. It is used in the synthesis of cresol, benzoic acid, etc. in addition to solvents, and is used for the production of benzene by demethylation.
안료: 색소로서 폴리우레탄(PU: Poly Urethane)과 배합되어 다양한 색상을 연출한다.Pigment: It is blended with polyurethane (PU: Poly Urethane) as coloring material and produces various colors.
이형지(R.P.: Release Paper): 종이 위에 폴리에칠렌(Poly Ethylene)을 코팅하여 다양한 음각무늬가 음각 되어 있으며, 이 음각무늬에 따라 완제품의 표면 무늬가 결정된다. R.P .: release paper: Polyethylene is coated on paper, and various engraved patterns are engraved, and the engraved pattern determines the surface pattern of the finished product.
본 발명을 실시함에 있어서는, 폴리에틸렌, 폴리스티렌, 폴리프로필렌 등의 석유화학 제품으로부터 얻어지고, 인체에 무해하며 우수한 탄성과 강도를 가지므로 건축자재, 포장재, 생활 소품 등으로 광범위하게 사용되는 고분자 물질인 폴리우레탄(Poly Urethane)과, 극성 유기용매의 하나로 각종 화학반응의 용매로 이용되며, 특히 고분자화합물인 폴리아크릴로나이트릴의 뛰어난 용제(溶劑)로 합성섬유의 방사용제(紡絲溶劑)로 이용되는 다이메틸폼아마이드(D.M.F : Dimethyl Formamide)와, 부틸알코올의 산화로 얻어지고 니트로셀룰로오스, 비닐 수지, 질산셀룰로오스 등의 용제로 쓰이는 메틸에틸케톤(M.E.K:methyl ethyl ketone)과, 색상을 창출하기 위한 안료를 배합하여 스킨(skin) 소재를 얻는 스킨배합공정과; 상기 고분자 물질인 폴리우레탄(Poly Urethane)과, 다이메틸폼아마이드(D.M.F : Dimethyl Formamide)와, 메틸에틸케톤(M.E.K:methyl ethyl ketone)과, 벤젠의 메틸 치환체로 물에는 녹지 않지만 에탄올에테르벤젠 등 대부분의 유기 용매와는 혼합되고 용제용 외에 크레졸, 벤조산 등의 합성에 사용되며 탈메틸 반응에 의한 벤젠 제조에 쓰여지는 희석제인 톨루엔(Toluene)을 배합하여 접착제를 얻는 접착제 배합공정과; 종이에 코팅한 폴리에틸렌(Poly Ethylene)의 표면에 다양한 음각무늬를 형성한 이형지(Release Paper)를 선택하여 이형지 롤을 구비하는 이형지 선택공정과; 상기 이형지 선택공정에서 선택한 이형지의 다양한 음각무늬가 형성된 표면에, 상기 스킨배합공정에서 얻어진 스킨을 균일한 두께로 도포하는 스킨도포공정과; 상기 스킨도포공정에서 음각무늬가 형성된 표면에 도포하여 스킨을 형성한 상태에서 건조챔버에서 희석제인 다이메틸폼아마이드(D.M.F : Dimethyl Formamide)와, 메틸에틸케톤(M.E.K:methyl ethyl ketone)의 성분을 증발하여 날려보내고 안료와 배합하여 색상을 창출하는 고분자 물질인 폴리우레탄(Poly Urethane)만으로 건조성형된 스킨을 형성하는 스킨성형건조공정과; 상기 스킨성형건조공정에서 건조성형된 스킨의 표면에 상기 접착제 배합공정에서 얻어진 접착제를 도포하는 접착제도포공정과; 상기 접착제도포공정에서 스킨의 표면에 도포한 접착제를 건조챔버에서 희석제인 다이메틸폼아마이드(D.M.F : Dimethyl Formamide)와, 메틸에틸케톤(M.E.K:methyl ethyl ketone)과, 희석제인 톨루엔(Toluene)의 성분을 증발하여 날려보내서 끈적끈적한 상태의 폴리우레탄(Poly Urethane)접착층을 형성하는 접착제건조공정과; 상기한 공정으로 다양한 음각무늬를 형성한 이형지(Release Paper)의 표면에 고분자 물질인 폴리우레탄(Poly Urethane)만으로 성형된 스킨을 형성하고, 상기 스킨의 표면에 형성한 끈적끈적한 상태의 폴리우레탄(Poly Urethane) 접착층 위에 직포나 부직포로 된 원단을 덮어서 폴리우레탄 접착제가 상기 원단에 일체로 침투하여 접합하도록 압착롤러로 압착하는 원단전사공정과; 상기 원단전사공정에서 스킨의 표면에 형성한 폴리우레탄(Poly Urethane) 접착층의 폴리우레탄 접착제가 상기 원단에 일체로 침투하여 스킨과 원단이 일체로 접합한 상태에서 롤 상태로 감아주는 원단롤링공정과; 상기 원단롤링공정에서 롤 상태로 감긴 상태에서 숙성챔버에서 잔여 다이메틸폼아마이드(D.M.F : Dimethyl Formamide)와, 메틸에틸케톤(M.E.K:methyl ethyl ketone)과, 희석제인 톨루엔(Toluene)의 성분을 완전히 증발하여 날려보내서 끈적끈적한 상태의 폴리우레탄(Poly Urethane)접착제를 경화시킴으로써 원단과 스킨이 일체가 되도록 접합숙성시키는 숙성공정과; 상기 숙성공정에서 접착제가 완전히 경화되어 원단과 스킨이 일체로 된 상태에서 이형지를 스킨의 표면에서 분리하는 이형지 분리공정;에 In carrying out the present invention, it is obtained from petroleum products such as polyethylene, polystyrene, and polypropylene, and is harmless to the human body and has excellent elasticity and strength. Therefore, the poly It is used as a solvent for various chemical reactions as a polyurethane and a polar organic solvent. Especially, it is used as a spinning solvent for synthetic fibers as an excellent solvent for polyacrylonitrile which is a polymer compound. Dimethyl formamide (DMF), methyl ethyl ketone (MEK: methyl ethyl ketone) obtained by oxidation of butyl alcohol and used as a solvent for nitrocellulose, vinyl resin and cellulose nitrate, and a pigment To obtain a skin material; The above polymer materials, such as polyurethane, dimethyl formamide (DMF), methyl ethyl ketone (MEK) and methyl substitution products of benzene, which are insoluble in water, An adhesive compounding step of blending with an organic solvent of toluene, toluene (toluene), which is used in the synthesis of cresol, benzoic acid, and the like, and diluent used in benzene production by demethylation, to obtain an adhesive; A releasing paper selection step of selecting a release paper having various engraved patterns formed on the surface of polyethylene (Poly Ethylene) coated on a paper to provide a releasing paper roll; A skin applying step of applying the skins obtained in the skin mixing step to a uniform thickness on a surface having various engraved patterns of the release paper selected in the release paper selecting step; (DMF) and methyl ethyl ketone (MEK: methyl ethyl ketone) are evaporated in a drying chamber in a state where the skin is formed by applying the composition on the engraved surface in the skin applying step, A skin forming drying step of forming a dry molded skin with polyurethane (Poly Urethane), which is a polymer material that blends with pigments and creates color by mixing with pigments; An adhesive applying step of applying the adhesive obtained in the adhesive compounding step to the surface of the skin that has been dry-molded in the skin molding and drying step; The adhesive applied on the surface of the skin in the adhesive application step is applied to the surface of the skin in a dry chamber by using a diluent such as dimethyl formamide (DMF), methyl ethyl ketone (MEK) and toluene (Toluene) To form a polyurethane (Urethane) adhesive layer in a sticky state; In the process described above, a skin formed of only polyurethane (Poly Urethane), which is a polymer material, is formed on the surface of a release paper on which various engraved patterns are formed, and the skin formed of a sticky polyurethane A cloth transferring step of covering a fabric made of a woven fabric or a nonwoven fabric on the adhesive layer, and pressing the same with a pressing roller so that the polyurethane adhesive penetrates and adheres integrally with the fabric; A raw material rolling process in which a polyurethane adhesive of a polyurethane adhesive layer formed on the surface of the skin in the fabric transferring step is integrally infiltrated into the fabric so that the skin and the fabric are integrally joined and wound in a roll state; The components of residual dimethylformamide (DMF), methyl ethyl ketone (MEK) and toluene (Toluene) as a diluent are completely evaporated in the aging chamber while being wound in the roll state in the raw rolling process To agitate the fabric so that the fabric and the skin are united with each other by curing the polyurethane adhesive in a sticky state; A release paper separating step of separating the release paper from the surface of the skin in a state where the adhesive is fully cured in the aging step and the fabric and the skin are integrated;
공간온도 180℃에서 분당 10m 씩 통과시키면서 간접 히터열로 분사식으로 불어주어서 스킨 원단으로부터 추출되는 총휘발성유기화합물(TVOC), 톨루엔(Toluene), 포름알데히이드(Formaldehyde) 등의 유해물질인 환경호르몬을 다수의 환풍기로 불어내어 제거하는 환경호르몬 제거 공정과;(TVOC), toluene (Toluene), and formaldehyde (Formaldehyde), which are extracted from the skin fabric by blowing with an indirect heater heat while passing through the room at a room temperature of 180 ° C for 10 m / An environmental hormone removing step of blowing off the foreign substances to a plurality of ventilators;
상기 환경호르몬 제거공정에서 환경호르몬이 제거된 스킨을 200℃의 간접열로 표면을 가열하고 180℃의 직접열로 이면을 가열한 다음 급랭하여 표면 조직이 조밀하게 재결정되어 스킨의 내부에 함유된 잔여 유해물질인 환경호르몬이 외부로 누출되지 않도록 처리하는 환경호르몬 차폐공정을 더 실시하여 이루어지는 폴리우레탄 스킨 원단 제조방법으로, 직포나 부직포로 된 원단에; 폴리우레탄(Poly Urethane) 55~55중량%와, 톨루엔(Toluene) 25~35중량%, 다이메틸폼아마이드(D.M.F : Dimethyl Formamide) 5~15중량%, 메틸에틸케톤(M.E.K:methyl ethyl ketone) 5~15중량%를 배합하여 얻어진 접착제로; 폴리우레탄(Poly Urethane) 15~25중량%와, 메틸에틸케톤(M.E.K:methyl ethyl ketone) 45~55중량%, 다이메틸폼아마이드(D.M.F : Dimethyl Formamide) 20~30중량%와 안료 2~8중량%를 배합하여 얻어진 0.1~0.3mm 두께의 스킨;을 일체로 접합하여 이루어지는 폴리우레탄 스킨 원단을 다시 풀어서 180℃로 가열하고 열풍을 분사하여 의 열간롤러나 열간챔버를 분당 10m 씩 통과시키면서 간접열 분사식으로 스킨 원단에 직접열풍을 불어서 스킨 원단으로부터 추출되는 유해물질인 환경호르몬이 제거되고 나머지 잔여 유해물질인 환경호르몬이 누출되지 않도록, 스킨 원단을 200℃의 간접열로 표면을 가열하고 180℃의 직접열로 이면을 가열한 다음 급랭하여 표면 조직이 조밀하게 구성한 친환경 폴리우레탄 스킨 원단을 구성한다. The surface of the skin from which the environmental hormone was removed in the environmental hormone removal step was heated by indirect heat at 200 ° C, heated by direct heat at 180 ° C, and then quenched to densely recrystallize the surface texture. A method for producing a polyurethane skin fabric, which comprises applying an environmental hormone shielding process for treating an environmental hormone which is a harmful substance so as not to leak to the outside, wherein the fabric is made of a woven fabric or a nonwoven fabric; A mixture of 55 to 55% by weight of polyurethane, 25 to 35% by weight of toluene, 5 to 15% by weight of dimethylformamide (DMF), 5 to 15% by weight of methyl ethyl ketone (MEK) By weight to 15% by weight; 15 to 25% by weight of polyurethane, 45 to 55% by weight of methyl ethyl ketone (MEK), 20 to 30% by weight of dimethylformamide (DMF) and 2 to 8% by weight of pigment And a skin of 0.1 to 0.3 mm in thickness obtained by blending together a polyurethane skin fabric having a thickness of 0.1 to 0.3 mm obtained by unifying the polyurethane skin fabric. The polyurethane skin fabric was heated again to 180 DEG C and hot air was blown thereon. The surface of the skin fabric is heated by indirect heat of 200 ° C so that the environmental hormone which is a harmful substance extracted from the skin fabric is blown by blowing hot air directly to the skin fabric and the remaining residual harmful substance, The surface of the back surface is heated and quenched to form an environmentally friendly polyurethane skin fabric having a dense surface structure.
여기서, 상기 스킨 배합공정에서, 폴리우레탄(Poly Urethane) 15~25중량%와, 메틸에틸케톤(M.E.K:methyl ethyl ketone) 45~55중량%, 다이메틸폼아마이드(D.M.F : Dimethyl Formamide) 20~30중량%와 안료 2~8중량%를 배합하여 조성하며, 상기 접착제 배합공정에서, 폴리우레탄(Poly Urethane) 55~55중량%와, 톨루엔(Toluene) 25~35중량%, 다이메틸폼아마이드(D.M.F : Dimethyl Formamide) 5~15중량%, 메틸에틸케톤(M.E.K:methyl ethyl ketone) 5~15중량%를 배합하여 조성한다.15 to 25% by weight of polyurethane, 45 to 55% by weight of methyl ethyl ketone (MEK), 20 to 30% by weight of dimethylformamide (DMF) in the skin mixing step, And 55 to 55% by weight of polyurethane, 25 to 35% by weight of toluene, 25 to 35% by weight of dimethylformamide (DMF (dimethylformamide)), : 5 to 15% by weight of dimethyl formamide, and 5 to 15% by weight of methyl ethyl ketone (MEK).
이때, 상기 원단롤링공정에서, 원단전사공정에서 스킨의 표면에 형성한 폴리우레탄(Poly Urethane)접착층의 폴리우레탄 접착제가 상기 원단에 일체로 침투하여 스킨과 원단이 일체로 접합한 상태에서, 상기 원단의 표면과 이형지 사이에 한지를 끼워서 감아주면 더욱 효과적이다.At this time, in the far-end rolling process, in the state where the polyurethane adhesive of the polyurethane (polyurethane) adhesive layer formed on the surface of the skin in the far-end transferring process is integrally infiltrated into the fabric and the skin and the fabric are integrally joined, It is more effective to wrap the paper between the surface of the paper and the release paper.
또한, 상기 스킨도포공정에서 스킨의 두께를 0.1~0.3mm로 하며, 상기 스킨성형건조공정에서 건조온도를 110℃~120℃로 유지하며, 상기 접착제도포공정에서 접착제의 두께를 두께를 0.1~0.3mm로 하며, 상기 접착제도포공정에서 접착제를 0.1~0.3mm 두께로 도포하며, 상기 접착제건조공정에서 건조온도를 120℃~140℃로 유지하며, 상기 숙성공정에서 숙성온도를 80℃~90℃로 유지하며 12시간 숙성하도록 한다.The thickness of the skin is 0.1 to 0.3 mm in the skin applying step, the drying temperature is maintained at 110 to 120 ° C in the skin molding drying step, and the thickness of the adhesive in the adhesive applying step is 0.1 to 0.3 the adhesive is applied in a thickness of 0.1 to 0.3 mm in the adhesive applying step and the drying temperature is maintained at 120 to 140 DEG C in the adhesive drying step and the aging temperature is adjusted to 80 to 90 DEG C Keep it for 12 hours.
특히, 상기 환경호르몬 제거 공정은, 원단과 스킨이 일체 접합되어 롤 상태로 감긴 스킨 원단을 풀어서 180℃의 열간롤러나 열간챔버를 분당 10m 씩 통과시키면서 가열한 다음, 간접열 분사식으로 스킨 원단에 직접 열풍을 불어서 스킨 원단으로부터 추출되는 총 휘발성 유기화합물(TVOC), 톨루엔(Toluene), 포름알데히이드(Formaldehyde)를 포함한 유해물질인 환경호르몬을 환풍기로 불어내어 제거하도록 하며, 상기 환경호르몬 차폐공정은, 환경호르몬 제거공정에서 환경호르몬이 제거된 스킨 원단을 200℃의 간접열로 표면을 가열하고 180℃의 직접열로 이면을 가열한 다음 급랭하여 표면 조직이 조밀하게 재결정되어 스킨의 내부에 함유된 잔여 유해물질인 환경호르몬이 외부로 누출되지 않도록 차폐처리한다.Particularly, in the environmental hormone removing process, the fabric and the skin are integrally joined together and the skin fabric wound in a rolled state is loosened, heated by passing the hot roller and the hot chamber at 180 ° C for 10 m per minute, The environmental hormone, which is a harmful substance including total volatile organic compounds (TVOC), toluene and formaldehyde extracted from the skin fabric by blowing hot air, is blown out by a ventilator, , The surface of the skin fabric in which the environmental hormone was removed in the process of removing the environmental hormone was heated by indirect heat at 200 ° C, the back surface was heated by direct heat at 180 ° C, and then quenched to densely recrystallize the surface texture. The remaining harmful substances, the environmental hormones, are shielded from leakage to the outside.
상기한 본 발명의 실시예를 공정별로 상세히 설명하면 다음과 같다.Hereinafter, embodiments of the present invention will be described in detail.
스킨배합공정;Skin mixing process;
폴리에틸렌, 폴리스티렌, 폴리프로필렌 등의 석유화학 제품으로부터 얻어지고, 인체에 무해하며 우수한 탄성과 강도를 가지므로 건축자재, 포장재, 생활 소품 등으로 광범위하게 사용되는 고분자 물질인 폴리우레탄(Poly Urethane)과, 극성 유기용매의 하나로 각종 화학반응의 용매로 이용되며, 특히 고분자화합물인 폴리아크릴로나이트릴의 뛰어난 용제(溶劑)로 합성섬유의 방사용제(紡絲溶劑)로 이용되는 다이메틸폼아마이드(D.M.F : Dimethyl Formamide)와, 부틸알코올의 산화로 얻어지고 니트로셀룰로오스, 비닐 수지, 질산셀룰로오스 등의 용제로 쓰이는 메틸에틸케톤(M.E.K:methyl ethyl ketone)와, 색상을 창출하기 위한 안료를 배합하여 스킨(skin) 소재를 얻는다.Polyurethane (Poly Urethane), which is a polymer material widely used in construction materials, packaging materials, and life accessories since it is obtained from petrochemical products such as polyethylene, polystyrene, and polypropylene and is harmless to human body and has excellent elasticity and strength, As a polar organic solvent, it is used as a solvent for various chemical reactions. In particular, dimethylformamide (DMF), which is used as a spinning solvent for synthetic fibers as an excellent solvent for polyacrylonitrile, (Methyl ethyl ketone), which is obtained by oxidation of butyl alcohol and used as a solvent for nitrocellulose, vinyl resin, and cellulose nitrate, and a pigment for producing color, Material is obtained.
이때 배합비는 상기 폴리우레탄(Poly Urethane) 15~25중량%와, 다이메틸폼아마이드(D.M.F : Dimethyl Formamide) 20~30중량%와, 메틸에틸케톤(M.E.K:methyl ethyl ketone) 45~55중량%와, 안료 2~8중량%를 배합하는 것으로, 본 발명인이 많은 실험으로 얻어낸 결과에 따른 가장 적합한 배합비는, 폴리우레탄(Poly Urethane) 20중량%와, 다이메틸폼아마이드(D.M.F : Dimethyl Formamide) 25중량%와, 메틸에틸케톤(M.E.K:methyl ethyl ketone) 50중량%와, 안료 5중량%를 배합하는 것이다.At this time, the compounding ratio is 15 to 25% by weight of the polyurethane, 20 to 30% by weight of dimethylformamide (DMF), 45 to 55% by weight of methyl ethyl ketone (MEK) By weight and 2 to 8% by weight of a pigment. The most suitable blending ratio according to the results obtained by the inventors of the present invention is 20% by weight of a polyurethane, 25% by weight of dimethylformamide (DMF) %, Methyl ethyl ketone (MEK: methyl ethyl ketone) 50% by weight, and pigment 5% by weight.
접착제 배합공정;Adhesive compounding process;
상기 고분자 물질인 폴리우레탄(Poly Urethane)과, 다이메틸폼아마이드(D.M.F : Dimethyl Formamide)와, 메틸에틸케톤(M.E.K:methyl ethyl ketone)와, 벤젠의 메틸 치환체로 물에는 녹지 않지만 에탄올에테르벤젠 등 대부분의 유기 용매와는 혼합되고 용제용 외에 크레졸, 벤조산 등의 합성에 사용되며 탈메틸 반응에 의한 벤젠 제조에 쓰여지는 희석제인 톨루엔(Toluene)을 배합하여 끈적끈적한 상태의 접착제를 얻는다. The above polymeric materials such as polyurethane, dimethyl formamide (DMF), methyl ethyl ketone (MEK) and methyl-substituted benzene, which are insoluble in water, (Toluene), which is a diluent used for the synthesis of cresol, benzoic acid and the like and used for the production of benzene by the demethylation reaction, is mixed with the organic solvent of the organic solvent to obtain a sticky adhesive.
이때 배합비는 고분자 물질인 폴리우레탄(Poly Urethane) 55~55중량%와, 다이메틸폼아마이드(D.M.F : Dimethyl Formamide) 5~15중량%와, 메틸에틸케톤(M.E.K:methyl ethyl ketone) 5~15중량%와, 희석제인 톨루엔(Toluene) 25~35중량%을 배합하는 것으로, 본 발명인이 많은 실험으로 얻어낸 결과에 따른 가장 적합한 배합비는, 폴리우레탄(Poly Urethane) 50중량%와, 다이메틸폼아마이드(D.M.F : Dimethyl Formamide) 10중량%와, 메틸에틸케톤(M.E.K:methyl ethyl ketone) 10중량%와, 희석제인 톨루엔(Toluene) 30중량%을 배합하는 것이다.At this time, the compounding ratio is 55 to 55% by weight of a polyurethane material (polyurethane), 5 to 15% by weight of dimethylformamide (DMF), 5 to 15% by weight of methyl ethyl ketone (MEK) By weight and 25 to 35% by weight of toluene as a diluent. According to the results obtained by the inventors of the present invention, the most appropriate blending ratio is 50% by weight of polyurethane (Urethane) and 50% by weight of dimethylformamide DMF: Dimethyl Formamide), 10% by weight of methyl ethyl ketone (MEK: methyl ethyl ketone), and 30% by weight of toluene (Toluene) as a diluent.
이형지 선택공정;A release paper selection process;
종이에 폴리에틸렌(Poly Ethylene)을 코팅한 표면에 스킨의 표면에 형성하고자 하는 다양한 음각무늬를 형성한 이형지(Release Paper)를 선택하여 이형지 롤을 구비한다. A release paper roll having a variety of engraving patterns to be formed on the surface of the skin is selected on the surface of polyethylene (Poly Ethylene) coated on the paper.
이때 이형지의 표면에 형성된 음각무늬는 완성된 스킨의 표면에 양각무늬로 나타날 것인바, 그 무늬형상 또한 다양한 것으로, 특별히 구애받지 않을 것이다.At this time, the engraved pattern formed on the surface of the release paper will appear as a relief pattern on the surface of the completed skin, and the shape of the pattern will also be not particularly limited.
또한 이때 사용되는 이형지는 스킨의 크기를 결정할 것인바, 본 발명인이 실시한 결과로는 폭은 1,700mm이고 길이는 1000m~2000m가 가장 적당하다.Also, the release paper used in this case determines the size of the skin, and as a result of the present invention, the width is 1,700 mm and the length is preferably 1000 m to 2000 m.
스킨도포공정;Skin application process;
상기 이형지 선택공정에서 선택한 이형지의 다양한 음각무늬가 형성된 표면에, 상기 스킨배합공정에서 얻어진 스킨을 균일한 두께로 도포한다. The skins obtained in the skin mixing step are applied on the surface of the release paper selected in the release paper selection step on the various engraved patterns in a uniform thickness.
이때 스킨의 두께는 0.1~0.3mm로 하는 것이 바람직하나, 본 발명인이 실시한 결과로는 0.15~0.2mm의 두께로 균일하게 도포하는 것이 가장 이상적이었다.At this time, it is preferable that the thickness of the skin is 0.1 to 0.3 mm, but as a result of the present invention, it is most preferable to uniformly coat the skin with a thickness of 0.15 to 0.2 mm.
상기한 이형지 표면에 스킨도포공정을 수행함에 있어서는, 이형지의 폭방향의 양측에 칸막이를 형성하여 스킨이 외부로 흘러나가지 못하게 한 다음 이형지를 이송하면서 스킨을 연속적으로 부어주고 나이프를 원하는 두께로 맞추어 스킨의 표면을 고르도록 함으로써 균일한 두께로 스킨을 음각무늬가 형성된 이형지표면에 도포한다.In performing the skin applying process on the surface of the release paper, a partition is formed on both sides in the width direction of the release paper so that the skin can not flow out. Then, the skin is continuously poured while transferring the release paper, So that the skin is uniformly applied to the surface of the mold surface on which the engraved pattern is formed.
스킨성형건조공정;A skin molding drying process;
상기 스킨도포공정에서 음각무늬가 형성된 이형지표면에 균일한 두께로 스킨을 도포하여 형성한 상태에서 건조챔버를 통과시켜서 희석제인 다이메틸폼아마이드(D.M.F : Dimethyl Formamide)와, 메틸에틸케톤(M.E.K:methyl ethyl ketone)의 성분을 증발하여 날려보내고 안료를 배합하여 색상을 창출하는 고분자 물질인 폴리우레탄(Poly Urethane)만으로 건조성형된 스킨을 형성한다.In the skin applying step, the skin is coated on the surface of the mold having the engraved pattern formed thereon with a uniform thickness, and the resulting mixture is passed through a drying chamber to form a mixture of dimethyl formamide (DMF) and methyl ethyl ketone Ethyl ketone is evaporated and blown away. Polyurethane (Poly Urethane), a polymer material that creates color by mixing pigments, forms a dry molded skin.
이때 상기 건조챔버의 온도는 100℃~140℃로 유지하는 것이 바람직하나 가장 이상적인 온도는 110℃~120℃이다. At this time, the temperature of the drying chamber is preferably maintained at 100 ° C to 140 ° C, but the most ideal temperature is 110 ° C to 120 ° C.
접착제도포공정;An adhesive application process;
상기 스킨성형건조공정에서 건조성형된 스킨의 표면에 상기 접착제 배합공정에서 얻어진 접착제를 균일한 두께로 도포한다.The adhesive obtained in the adhesive compounding step is applied to the surface of the skin that has been dry-molded in the skin molding and drying process to a uniform thickness.
이때 접착제의 두께는 스킨의 두께와 동일하게 하는 것으로 0.1~0.3mm로 하는 것이 바람직하나, 본 발명인이 실시한 결과로는 0.15~0.2mm의 두께로 균일하게 도포하는 것이 가장 이상적이었다.At this time, it is preferable that the thickness of the adhesive is 0.1 to 0.3 mm, which is equal to the thickness of the skin, but as a result of the present invention, it is most preferable to uniformly apply the adhesive to a thickness of 0.15 to 0.2 mm.
상기한 스킨의 표면에 접착제도포공정을 수행함에 있어서는, 이형지의 폭방향의 양측에 칸막이를 형성하여 접착제가 외부로 흘러나가지 못하게 한 다음 이형지에 성형된 스킨을 이송하면서 접착제를 연속적으로 부어주고 나이프를 원하는 두께로 맞추어 접착제의 표면을 고르도록 함으로써 균일한 두께로 접착제를 스킨의 표면에 도포한다. In performing the adhesive applying process on the surface of the skin, a partition is formed on both sides in the width direction of the release paper so that the adhesive does not flow out to the outside. Then, the skin is transferred to the release paper while continuously conveying the adhesive, The adhesive is applied to the surface of the skin at a uniform thickness by adjusting the thickness of the adhesive to the desired thickness.
접착제건조공정;Adhesive drying process;
상기 접착제도포공정에서 스킨의 표면에 도포한 접착제를 건조챔버를 통과시키면서 희석제인 다이메틸폼아마이드(D.M.F : Dimethyl Formamide)와, 메틸에틸케톤(M.E.K:methyl ethyl ketone) 성분을 완전히 증발시켜서 날려보내고, 희석제인 톨루엔(Toluene)의 성분을 증발하여 끈적끈적한 상태의 폴리우레탄(Poly Urethane)접착층을 형성한다. In the adhesive application step, the adhesive applied on the surface of the skin is completely blown off by passing the diluent (DMF: Dimethyl Formamide) and the methyl ethyl ketone (MEK: methyl ethyl ketone) The components of the diluent toluene are evaporated to form a sticky polyurethane adhesive layer.
이때 상기 건조챔버의 온도는 100℃~140℃로 유지하는 것이 바람직하나 가장 이상적인 온도는 120℃~130℃이다. At this time, the temperature of the drying chamber is preferably maintained at 100 ° C to 140 ° C, but the most ideal temperature is 120 ° C to 130 ° C.
원단전사공정;Fabric transfer process;
상기한 공정으로 다양한 음각무늬를 형성한 이형지(Release Paper)의 표면에 고분자 물질인 폴리우레탄(Poly Urethane)만으로 성형된 스킨을 형성하고, 상기 스킨의 표면에 형성한 끈적끈적한 상태의 폴리우레탄(Poly Urethane) 접착층 위에 직포나 부직포로 된 원단을 덮어서 폴리우레탄 접착제가 상기 원단에 일체로 침투하여 접합하도록 적어도 한 쌍 이상의 압착롤러로 압착한다.In the process described above, a skin formed of only polyurethane (Poly Urethane), which is a polymer material, is formed on the surface of a release paper on which various engraved patterns are formed, and the skin formed of a sticky polyurethane Urethane) The fabric is covered with a woven fabric or a nonwoven fabric on the adhesive layer, and is pressed with at least one or more pressing rollers so that the polyurethane adhesive penetrates and adheres integrally with the fabric.
이때 사용되는 직포는 직물로써 스킨과 일체로 접합성형되어 제품의 질을 결정하게 되므로 원가에 구애되지 않는 한 좋은 원단을 사용한다. In this case, the woven fabric used as the fabric is integrally formed with the skin to determine the quality of the product, so a good fabric is used as long as the cost is not adhered to.
원단롤링공정;Fabric rolling process;
상기 원단전사공정에서 스킨의 표면에 형성한 폴리우레탄(Poly Urethane)접착층의 폴리우레탄 접착제가 상기 원단에 일체로 침투하여 스킨과 원단이 일체로 접합한 상태에서 롤 상태로 감아준다.A polyurethane adhesive of a polyurethane (Urethane) adhesive layer formed on the surface of the skin in the fabric transferring step is integrally infiltrated into the fabric so that the skin and the fabric are rolled up in a state of being integrally joined.
여기서 상기 원단의 표면과 이형지 사이에 한지를 끼워서 감아주거나 원단을 1겹 더 끼워서 감아주면 접착제의 경화에 시간이 절감되는 것은 물론, 접착에 함유하고있는 유해물질이 빠지는 것을 촉진하여 보다 안정된 제품을 얻을 수 있다.In this case, it is possible to reduce the time for the curing of the adhesive by winding the paper between the surface of the fabric and the releasing paper by wrapping the paper together or by wrapping the cloth one more time, as well as promoting the release of the harmful substances contained in the adhesive, .
숙성공정;Aging process;
상기 원단롤링공정에서 롤 상태로 감긴 상태에서 숙성챔버에서 숙성시켜서 잔여 다이메틸폼아마이드(D.M.F : Dimethyl Formamide)와, 메틸에틸케톤(M.E.K:methyl ethyl ketone) 성분을 완전히 증발하여 날려보내는 것은 물론, 희석제인 톨루엔(Toluene)의 성분도 완전히 증발하여 날려보내서 끈적끈적한 상태의 폴리우레탄(Poly Urethane)접착제를 경화시킴으로써 원단과 스킨이 일체로 접합 되도록 접합숙성시킨다. In the raw rolling process, the resin is aged in an aging chamber in a rolled state to completely evaporate residual dimethylformamide (DMF) and methyl ethyl ketone (MEK) components, The components of toluene are completely evaporated and blown to cure the sticky Poly Urethane adhesive so that the fabric and the skin are mated together so as to be joined together.
이때 숙성챔버의 온도는 100℃ 이하를 유지하는 것이 바람직하며, 가장 이상적인 숙성온도는 80℃~90℃로 12시간 이상 숙성하는 것이 바람직하다.At this time, the temperature of the aging chamber is preferably maintained at 100 ° C or less, and the most ideal aging temperature is preferably aged at 80 ° C to 90 ° C for 12 hours or more.
여기서도 상기 원단롤링공정에서 원단의 표면과 이형지 사이에 한지를 끼워서 감아주거나 원단을 1겹 더 끼워서 감아주면 접착제의 다이메틸폼아마이드(D.M.F : Dimethyl Formamide)와, 메틸에틸케톤(M.E.K:methyl ethyl ketone) 성분과, 희석제인 톨루엔(Toluene) 성분이 상기한 한지나 원단을 타고 외부로 방출되어 완전히 날아가게 된다.In this case, if the fabric is rolled with a paper between the surface of the fabric and the releasing paper, or if the fabric is rolled up one by one, the adhesive of dimethyl formamide (DMF) and methyl ethyl ketone (MEK) And a toluene component as a diluent are discharged to the outside through the above-described Hanjina fabric and are completely blown away.
따라서 상기 원단의 표면과 이형지 사이에 끼워서 감아주는 원단은 발수성이 좋은 메시망으로 제직하면 더욱 효과적일 것이다.Therefore, the fabric which is sandwiched between the surface of the fabric and the releasing paper may be more effective if it is woven with a mesh cloth having good water repellency.
또한 상기 한지를 대신하여 일반적인 종이를 끼워서 감더라도 그 효과는 무시할 수 없다 할 것이다. In addition, even if a general paper is put in place in place of the paper, the effect thereof can not be neglected.
이형지 분리공정;Release paper separation process;
상기 숙성공정에서 접착제가 완전히 경화되어 원단과 스킨이 일체로 된 상태에서 이형지를 스킨의 표면에서 분리하여 스킨 원단만을 검사와 함께 롤로 감는다.In the aging process, the adhesive is fully cured and the release paper is separated from the surface of the skin in a state where the fabric and the skin are integrated, and only the skin fabric is inspected and rolled with a roll.
환경호르몬 제거공정;Environmental hormone removal process;
원단과 스킨이 일체로 접합되어 롤 상태로 감긴 스킨 원단을 풀어서 가열함과 동시에 열풍을 불어서 스킨 원단으로부터 추출되는 유해물질인 환경호르몬을 환풍기로 불어내어 제거한다.The cloth and the skin are joined together, and the skin fabric wound in the roll state is released and heated. At the same time, the environmental hormone which is extracted from the skin fabric by blowing hot air is blown out by a fan.
이때, 상기 환경호르몬 제거 공정은, 원단과 스킨이 일체 접합되어 롤 상태로 감긴 스킨 원단을 풀어서 180℃의 열간롤러나 열간챔버를 분당 10m 씩 통과시키면서 가열한 다음, 간접열 분사식으로 스킨 원단에 직접열풍을 불어서 스킨 원단으로부터 추출되는 총 휘발성 유기화합물(TVOC), 톨루엔(Toluene), 포름알데히이드(Formaldehyde)를 포함한 유해물질인 환경호르몬을 환풍기로 불어내어 제거함으로써 유해물질인 환경호르몬은 거의 전부가 제거된다.At this time, in the environmental hormone removing process, the fabric and the skin are integrally joined together and the skin fabric wound in a rolled state is loosened, heated by passing through a hot roller or a hot chamber at 180 ° C for 10 m per minute, and then directly heated Environmental hormones, which are harmful substances including total volatile organic compounds (TVOC), toluene, and formaldehyde, which are extracted from skin fabrics by blowing hot air, are blown out by a fan to remove almost all environmental hormones Is removed.
환경호르몬 차폐공정;Environmental hormone screening process;
상기 환경호르몬 제거공정에서 환경호르몬이 제거된 스킨 원단을 180℃~200℃로 가열한 다음 급랭하여 스킨 원단의 내부에 함유된 잔여 유해물질인 환경호르몬이 외부로 누출되지 않도록 처리한다.In the environmental hormone removing step, the skin material from which the environmental hormone has been removed is heated to 180 to 200 ° C, and quenched to treat the environment hormone, which is a residual harmful substance contained in the skin material, from leaking out.
이때, 상기 환경호르몬 차폐공정은, 환경호르몬 제거공정에서 환경호르몬이 제거된 스킨 원단을 200℃의 간접열로 표면을 가열하고 180℃의 직접열로 이면을 가열한 다음 15~20℃의 온도를 유지하는 챔버에 투입하여 급랭함으로써 표면 조직이 조밀하게 재결정되어 스킨 원단의 내부에 함유된 잔여 유해물질인 환경호르몬이 외부로 누출되지 않도록 차폐처리함으로써 사용중 유해물질인 환경호르몬이 외부로 누출되지 않는 친환경 폴리우레탄 스킨 원단을 제조한다. At this time, in the environmental hormone shielding step, the surface of the skin material in which the environmental hormone is removed in the environmental hormone removing step is heated by indirect heat at 200 ° C., the rear surface is heated by direct heat at 180 ° C., And the surface tissue is densely recrystallized by being quenched into the holding chamber so that the environmental hormone which is the residual harmful substance contained in the skin fabric is shielded from leaking to the outside so that the environment hormone which is a harmful substance during use does not leak to the outside A polyurethane skin fabric is produced.
상기한 실시공정에 따른 폴리우레탄 스킨 원단 제조방법으로, 직포나 부직포로 된 원단에; 폴리우레탄(Poly Urethane) 55~55중량%와, 톨루엔(Toluene) 25~35중량%, 다이메틸폼아마이드(D.M.F : Dimethyl Formamide) 5~15중량%, 메틸에틸케톤(M.E.K:methyl ethyl ketone) 5~15중량%를 배합하여 얻어진 접착제로; 폴리우레탄(Poly Urethane) 15~25중량%와, 메틸에틸케톤(M.E.K:methyl ethyl ketone) 45~55중량%, 다이메틸폼아마이드(D.M.F : Dimethyl Formamide) 20~30중량%와 안료 2~8중량%를 배합하여 얻어진 0.1~0.3mm 두께의 스킨;을 일체로 접합하여서 이루어지는 폴리우레탄 스킨 원단을 완성하고 이들 스킨 원단을 180℃로 가열하고 열풍을 분사하여 의 열간롤러나 열간챔버를 분당 10m 씩 통과시키면서 간접열 분사식으로 스킨 원단에 직접열풍을 불어서 스킨 원단으로부터 추출되는 유해물질인 환경호르몬이 제거되고 나머지 잔여 유해물질인 환경호르몬이 누출되지 않도록, 스킨 원단을 200℃의 간접열로 표면을 가열하고 180℃의 직접열로 이면을 가열한 다음 급랭하여 표면 조직이 조밀하게 구성한다.A method for producing a polyurethane skin fabric according to the above-described embodiment, comprising the steps of: A mixture of 55 to 55% by weight of polyurethane, 25 to 35% by weight of toluene, 5 to 15% by weight of dimethylformamide (DMF), 5 to 15% by weight of methyl ethyl ketone (MEK) By weight to 15% by weight; 15 to 25% by weight of polyurethane, 45 to 55% by weight of methyl ethyl ketone (MEK), 20 to 30% by weight of dimethylformamide (DMF) and 2 to 8% by weight of pigment % Of a skin having a thickness of 0.1 to 0.3 mm were integrally bonded to each other, and the skin fabric was heated to 180 DEG C, hot air was blown thereon, and the hot roller and the hot chamber were passed through at intervals of 10 m per minute The surface of the skin fabric is heated by indirect heat at 200 ° C so that the environmental hormone which is a harmful substance extracted from the skin fabric is removed by blowing hot air directly to the skin fabric by the indirect thermal spraying method and the remaining residual harmful substance, The back surface is heated with direct heat at 180 ° C and quenched to form a dense surface structure.
상기한 본 발명은 스킨 원단을 생산함에 있어서 잔여 환경호로몬이 외부로 누출되는 것을 최소화하여 건축자재, 포장재, 생활 소품 등에 즉시 실시할 수 있는 등 산업상 이용가치가 대단하다 할 것이다.The above-described present invention minimizes the leakage of the residual environmental hormone to the outside in the production of skin fabrics, so that it can be carried out immediately on building materials, packaging materials, and household items.
Claims (4)
상기 고분자 물질인 폴리우레탄(Poly Urethane)과, 다이메틸폼아마이드(D.M.F : Dimethyl Formamide)와, 메틸에틸케톤(M.E.K:methyl ethyl ketone)과, 벤젠의 메틸 치환체로 쓰여지는 희석제인 톨루엔(Toluene)을 배합하여 접착제를 얻는 접착제 배합공정과;
종이에 폴리에틸렌(Poly Ethylene)을 코팅한 표면에 다양한 음각무늬를 형성한 이형지(Release Paper)를 선택하여 이형지 롤을 구비하는 이형지 선택공정과;
상기 이형지 선택공정에서 선택한 이형지의 다양한 음각무늬가 형성된 표면에 상기 스킨배합공정에서 얻어진 스킨을 균일하게 도포하는 스킨도포공정과;
상기 스킨도포공정에서 음각무늬가 형성된 표면에 도포하여 스킨을 형성한 상태에서 건조챔버에서 희석제인 다이메틸폼아마이드(D.M.F : Dimethyl Formamide)와, 메틸에틸케톤(M.E.K:methyl ethyl ketone)의 성분을 증발하여 날려보내고 안료를 배합하여 색상을 창출하는 고분자 물질인 폴리우레탄(Poly Urethane)만으로 건조성형된 스킨을 형성하는 스킨성형건조공정과;
상기 스킨성형건조공정에서 건조성형된 스킨의 표면에 상기 접착제 배합공정에서 얻어진 접착제를 도포하는 접착제도포공정과;
상기 접착제도포공정에서 스킨의 표면에 도포한 접착제를 120℃~130℃의 건조챔버에서 희석제인 다이메틸폼아마이드(D.M.F : Dimethyl Formamide)와, 메틸에틸케톤(M.E.K:methyl ethyl ketone)과, 희석제인 톨루엔(Toluene)의 성분을 증발하여 날려보내서 끈적끈적한 상태의 폴리우레탄(Poly Urethane)접착층을 형성하는 접착제건조공정과;
상기한 공정으로 다양한 음각무늬를 형성한 이형지(Release Paper)의 표면에 고분자 물질인 폴리우레탄(Poly Urethane)만으로 성형된 스킨을 형성하고, 상기 스킨의 표면에 형성한 끈적끈적한 상태의 폴리우레탄(Poly Urethane)접착층 위에 직포나 부직포로 된 원단을 덮어서 폴리우레탄 접착제가 상기 원단에 일체로 침투하여 접합하도록 압착롤러로 압착하는 원단전사공정과;
상기 원단전사공정에서 스킨의 표면에 형성한 폴리우레탄(Poly Urethane)접착층의 폴리우레탄 접착제가 상기 원단에 일체로 침투하여 스킨과 원단이 일체로 접합한 상태에서 롤 상태로 감아주는 원단롤링공정과;
상기 원단롤링공정에서 롤 상태로 감긴 상태에서 80℃~90℃로 유지하는 숙성챔버에서 12시간 숙성시켜서 잔여 다이메틸폼아마이드(D.M.F : Dimethyl Formamide)와, 메틸에틸케톤(M.E.K:methyl ethyl ketone)과, 희석제인 톨루엔(Toluene)의 성분을 완전히 증발하여 날려보내서 끈적끈적한 상태의 폴리우레탄(Poly Urethane) 접착제를 경화시킴으로써 원단과 스킨이 일체가 되도록 접합숙성시키는 숙성공정과;
상기 숙성공정에서 접착제가 완전히 경화되어 원단과 스킨이 일체로 된 상태에서 이형지를 스킨의 표면에서 분리하는 이형지 분리공정;에,
원단과 스킨이 일체로 접합되어 롤 상태로 감긴 스킨 원단을 풀어서 가열함과 동시에 열풍을 불어서 스킨 원단으로부터 추출되는 유해물질인 환경호르몬을 환풍기로 불어내어 제거하는 환경호르몬 제거 공정과;
상기 환경호르몬 제거공정에서 환경호르몬이 제거된 스킨 원단을 180℃~200℃로 가열한 다음 급랭하여 스킨 원단의 내부에 함유된 잔여 유해물질인 환경호르몬이 외부로 누출되지 않도록 처리하는 환경호르몬 차폐공정을; 더 실시하여 이루어짐을 특징으로 하는 친환경 폴리우레탄 스킨 원단 제조방법.Polyurethane (Poly Urethane) which is a polymer material and dimethyl formamide (DMF) which is used as a spinning solvent of synthetic fiber with a solvent which is a polymer compound are obtained by oxidation of butyl alcohol A skin mixing process for obtaining a skin material by blending methyl ethyl ketone (MEK: methyl ethyl ketone) used as a solvent and a pigment;
The above polymer material, polyurethane, dimethyl formamide (DMF), methyl ethyl ketone (MEK), and toluene (Toluene), which is a diluent used as a methyl substituent of benzene, An adhesive compounding step of compounding the adhesive to obtain an adhesive;
A releasing paper selection step of selecting a release paper having various engraved patterns on a surface of polyethylene (Poly Ethylene) coated on a paper sheet to provide a releasing paper roll;
A skin applying step of uniformly applying the skins obtained in the skin mixing step to the surface of the release paper selected in the release paper selecting step;
(DMF) and methyl ethyl ketone (MEK: methyl ethyl ketone) are evaporated in a drying chamber in a state where the skin is formed by applying the composition on the engraved surface in the skin applying step, A skin forming drying step of forming a dry-formed skin with polyurethane (Poly Urethane), which is a polymer material that blows away and forms a color by blending pigments;
An adhesive applying step of applying the adhesive obtained in the adhesive compounding step to the surface of the skin that has been dry-molded in the skin molding and drying step;
The adhesive applied on the surface of the skin in the adhesive application step is coated with a diluent such as dimethyl formamide (DMF), methyl ethyl ketone (MEK) and methyl ethyl ketone (diluent) in a drying chamber at 120 ° C to 130 ° C, An adhesive drying step of evaporating a component of toluene and blowing it to form a sticky sticky polyurethane (Urethane) adhesive layer;
In the process described above, a skin formed of only polyurethane (Poly Urethane), which is a polymer material, is formed on the surface of a release paper on which various engraved patterns are formed, and the skin formed of a sticky polyurethane A cloth transferring step of covering a fabric made of a woven fabric or a nonwoven fabric on the adhesive layer, and pressing the same with a pressing roller so that the polyurethane adhesive penetrates and adheres integrally with the fabric;
A raw material rolling process in which a polyurethane adhesive of a polyurethane adhesive layer formed on the surface of the skin in the fabric transferring step is integrally infiltrated into the fabric so that the skin and the fabric are integrally joined and wound in a roll state;
After aging for 12 hours in an aging chamber maintained at 80 ° C to 90 ° C in a rolled state in the far-end rolling process, residual DMF (dimethyl formamide), methyl ethyl ketone (MEK) , Aging the components of the diluent toluene (Toluene) completely evaporated and blowing them to cure the sticky sticky polyurethane (Urethane) adhesive so that the fabric and the skin are integrated;
A release paper separating step of separating the release paper from the surface of the skin in a state where the adhesive is completely cured in the aging step and the fabric and the skin are integrated,
An environmental hormone removing step for removing the environmental hormone, which is a harmful substance extracted from the skin fabric by blowing hot air while blowing hot and heating the skin fabric which is rolled up in a rolled state by blowing with a ventilator;
An environmental hormone screening process in which the skin material from which the environmental hormone has been removed in the environmental hormone removing process is heated to 180 ° C to 200 ° C and quenched to treat the environment hormone which is a residual harmful substance contained in the skin material, of; Wherein the method further comprises the steps of:
상기 환경호르몬 제거 공정은, 원단과 스킨이 일체 접합되어 롤 상태로 감긴 스킨 원단을 풀어서 180℃의 열간롤러나 열간챔버를 분당 10m 씩 통과시키면서 가열한 다음, 간접열 분사식으로 스킨 원단에 직접열풍을 불어서 스킨 원단으로부터 추출되는 총 휘발성 유기화합물(TVOC), 톨루엔(Toluene), 포름알데히이드(Formaldehyde)를 포함한 유해물질인 환경호르몬을 환풍기로 불어내어 제거하는 것을 특징으로 하는 친환경 폴리우레탄 스킨 원단 제조방법.The method according to claim 1,
In the environmental hormone removing process, the cloth and the skin are integrally joined together and the skin fabric wound in a rolled state is loosened. The cloth is heated while passing through a hot roller or a hot chamber at 180 ° C for 10 m per minute, and hot air is directly blown Environmentally friendly polyurethane skin fabrication characterized by blowing out environmental hormones, which are harmful substances including total volatile organic compounds (TVOC), toluene, and formaldehyde, extracted from blown skin fabrics by a blower Way.
상기 환경호르몬 차폐공정은, 환경호르몬 제거공정에서 환경호르몬이 제거된 스킨 원단을 200℃의 간접열로 표면을 가열하고 180℃의 직접열로 이면을 가열한 다음 15~25℃의 챔버로 투입하여 급랭함으로써 표면 조직이 조밀하게 재결정되어 스킨의 내부에 함유된 잔여 유해물질인 환경호르몬이 외부로 누출되지 않도록 차폐처리하는 것을 특징으로 하는 친환경 폴리우레탄 스킨 원단 제조방법.The method according to claim 1,
In the environmental hormone screening process, the surface of the skin having the environment hormone removed in the environmental hormone removing process is heated by indirect heat at 200 ° C, Wherein the surface tissue is densely recrystallized by quenching so that the environmental hormone which is a residual harmful substance contained in the skin is shielded so as not to leak to the outside.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020150024962A KR101599399B1 (en) | 2015-02-23 | 2015-02-23 | Green polyurethane skin material and a method of manufacturing |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020150024962A KR101599399B1 (en) | 2015-02-23 | 2015-02-23 | Green polyurethane skin material and a method of manufacturing |
Publications (1)
Publication Number | Publication Date |
---|---|
KR101599399B1 true KR101599399B1 (en) | 2016-03-03 |
Family
ID=55535631
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1020150024962A Active KR101599399B1 (en) | 2015-02-23 | 2015-02-23 | Green polyurethane skin material and a method of manufacturing |
Country Status (1)
Country | Link |
---|---|
KR (1) | KR101599399B1 (en) |
Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR870700424A (en) | 1984-09-17 | 1987-12-29 | Molding medium and method for manufacturing the same | |
KR20000011476A (en) | 1998-07-06 | 2000-02-25 | 나카무라 하사오 | Thermoplastic polyurethanes, polyurethane elastic fibers therefrom, and method for producing the fibers |
KR20050039065A (en) * | 2003-10-23 | 2005-04-29 | 서상우 | Manufacturing method of artificial leather having soft surface |
KR20060096222A (en) | 2005-03-04 | 2006-09-11 | 최해용 | Left and Right Cross Removable Screen Unit |
KR20090015089A (en) | 2006-05-31 | 2009-02-11 | 세프라코 아이엔시. | Method of treating pain disorder by trans 4- (3,4-dichlorophenyl) -1,2,3,4-tetrahydro-1-naphthalenamine and its formamide |
KR20090081961A (en) | 2008-01-25 | 2009-07-29 | 삼경무역 주식회사 | Horse gagged |
KR20110041522A (en) | 2008-07-30 | 2011-04-21 | 미쓰이 가가쿠 가부시키가이샤 | Polyester polyols, compositions for polyurethanes, compositions for polyurethane foams, polyurethane resins and polyurethane foams |
KR20120004004A (en) | 2010-07-06 | 2012-01-12 | 염인철 | Vertical Grinder |
KR101434918B1 (en) * | 2014-06-05 | 2014-08-29 | 성일티앤씨 주식회사 | Method for manufacturing synthetic leather and synthetic leather manufacture by using the same |
KR101448133B1 (en) * | 2014-02-27 | 2014-10-07 | (주)두올상사 | A method of manufacturing the polyurethane skin fabric and the polyurethane skin fabric |
-
2015
- 2015-02-23 KR KR1020150024962A patent/KR101599399B1/en active Active
Patent Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR870700424A (en) | 1984-09-17 | 1987-12-29 | Molding medium and method for manufacturing the same | |
KR20000011476A (en) | 1998-07-06 | 2000-02-25 | 나카무라 하사오 | Thermoplastic polyurethanes, polyurethane elastic fibers therefrom, and method for producing the fibers |
KR20050039065A (en) * | 2003-10-23 | 2005-04-29 | 서상우 | Manufacturing method of artificial leather having soft surface |
KR20060096222A (en) | 2005-03-04 | 2006-09-11 | 최해용 | Left and Right Cross Removable Screen Unit |
KR20090015089A (en) | 2006-05-31 | 2009-02-11 | 세프라코 아이엔시. | Method of treating pain disorder by trans 4- (3,4-dichlorophenyl) -1,2,3,4-tetrahydro-1-naphthalenamine and its formamide |
KR20090081961A (en) | 2008-01-25 | 2009-07-29 | 삼경무역 주식회사 | Horse gagged |
KR20110041522A (en) | 2008-07-30 | 2011-04-21 | 미쓰이 가가쿠 가부시키가이샤 | Polyester polyols, compositions for polyurethanes, compositions for polyurethane foams, polyurethane resins and polyurethane foams |
KR20120004004A (en) | 2010-07-06 | 2012-01-12 | 염인철 | Vertical Grinder |
KR101448133B1 (en) * | 2014-02-27 | 2014-10-07 | (주)두올상사 | A method of manufacturing the polyurethane skin fabric and the polyurethane skin fabric |
KR101434918B1 (en) * | 2014-06-05 | 2014-08-29 | 성일티앤씨 주식회사 | Method for manufacturing synthetic leather and synthetic leather manufacture by using the same |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN108948313B (en) | Environment-friendly artificial leather for automobile interior and manufacturing method thereof | |
KR100201975B1 (en) | Thermoplastic polyurethanes and molded articles comprising them | |
KR101418485B1 (en) | Polymer blend composition based on the carbon dioxide polymers and the environment friendly decorating materials using it | |
JP4168205B2 (en) | Leather-like sheet | |
CN101410473B (en) | Moisture-curable polyurethane hot melt adhesive and multilayer sheet using the same | |
JP4184178B2 (en) | Thermoplastic polymer composition | |
JP5970154B2 (en) | Aqueous dispersion and method of using it for production of sheet-like substrate | |
KR101448133B1 (en) | A method of manufacturing the polyurethane skin fabric and the polyurethane skin fabric | |
TW201319355A (en) | Artificial leather with improved flexing endurance properties | |
JP2009538938A (en) | Method for producing flexible composite elastomeric polyurethane skin | |
KR102693250B1 (en) | Synthetic leather for crash pad and preparation method thereof | |
KR20100075668A (en) | Polyurethane composition | |
JP4710494B2 (en) | Moisture curable polyurethane hot melt composition | |
JP5405383B2 (en) | Flame retardant urethane resin and flame retardant synthetic leather | |
CN113788925A (en) | Waterborne polyurethane resin and preparation method and application thereof | |
KR100985513B1 (en) | The composition and manufacturing method for solventborne type polyurethane resin has good emboss moulding | |
JP2011241528A (en) | Synthetic leather | |
KR101599399B1 (en) | Green polyurethane skin material and a method of manufacturing | |
CN1359965A (en) | Porous polyurethane and mfg. method therefor | |
JP4408778B2 (en) | Synthetic leather | |
WO2022191102A1 (en) | Curable composition and synthetic leather | |
JP6769570B2 (en) | Urethane resin composition and laminate | |
JP4408750B2 (en) | Synthetic leather | |
JP4541788B2 (en) | Synthetic leather | |
KR102641079B1 (en) | A polyurethane skin resin composition for pet film and its manufacturing method |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PA0109 | Patent application |
Patent event code: PA01091R01D Comment text: Patent Application Patent event date: 20150223 |
|
PA0201 | Request for examination | ||
E701 | Decision to grant or registration of patent right | ||
PE0701 | Decision of registration |
Patent event code: PE07011S01D Comment text: Decision to Grant Registration Patent event date: 20160218 |
|
GRNT | Written decision to grant | ||
PR0701 | Registration of establishment |
Comment text: Registration of Establishment Patent event date: 20160225 Patent event code: PR07011E01D |
|
PR1002 | Payment of registration fee |
Payment date: 20160225 End annual number: 3 Start annual number: 1 |
|
PG1601 | Publication of registration | ||
FPAY | Annual fee payment |
Payment date: 20191224 Year of fee payment: 5 |
|
PR1001 | Payment of annual fee |
Payment date: 20191224 Start annual number: 5 End annual number: 5 |
|
PR1001 | Payment of annual fee |
Payment date: 20201210 Start annual number: 6 End annual number: 6 |
|
PR1001 | Payment of annual fee |
Payment date: 20221222 Start annual number: 8 End annual number: 8 |
|
PR1001 | Payment of annual fee |
Payment date: 20240118 Start annual number: 9 End annual number: 9 |
|
PR1001 | Payment of annual fee |
Payment date: 20250317 Start annual number: 10 End annual number: 10 |