EP2859145A2 - Textilhilfsmittel und damit veredeltes textilprodukt - Google Patents
Textilhilfsmittel und damit veredeltes textilproduktInfo
- Publication number
- EP2859145A2 EP2859145A2 EP13729627.3A EP13729627A EP2859145A2 EP 2859145 A2 EP2859145 A2 EP 2859145A2 EP 13729627 A EP13729627 A EP 13729627A EP 2859145 A2 EP2859145 A2 EP 2859145A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- fibers
- acrylate
- textile
- meth
- group
- 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.)
- Granted
Links
- 239000004753 textile Substances 0.000 title claims abstract description 81
- 239000012752 auxiliary agent Substances 0.000 title abstract 2
- -1 tissues Substances 0.000 claims abstract description 47
- 239000004744 fabric Substances 0.000 claims abstract description 17
- 239000004745 nonwoven fabric Substances 0.000 claims abstract description 3
- 239000004065 semiconductor Substances 0.000 claims description 30
- 229920000642 polymer Polymers 0.000 claims description 20
- 239000000835 fiber Substances 0.000 claims description 18
- 239000000203 mixture Substances 0.000 claims description 18
- 239000011230 binding agent Substances 0.000 claims description 17
- 239000004814 polyurethane Substances 0.000 claims description 17
- 229920002635 polyurethane Polymers 0.000 claims description 17
- 150000001875 compounds Chemical class 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 12
- 238000010521 absorption reaction Methods 0.000 claims description 10
- 239000002253 acid Substances 0.000 claims description 10
- 229920000767 polyaniline Polymers 0.000 claims description 9
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 8
- 238000000576 coating method Methods 0.000 claims description 8
- 229910052782 aluminium Inorganic materials 0.000 claims description 7
- 239000011248 coating agent Substances 0.000 claims description 7
- 239000000499 gel Substances 0.000 claims description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 6
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 6
- 150000007513 acids Chemical class 0.000 claims description 6
- 239000000975 dye Substances 0.000 claims description 6
- 229910052738 indium Inorganic materials 0.000 claims description 6
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 claims description 6
- SKRWFPLZQAAQSU-UHFFFAOYSA-N stibanylidynetin;hydrate Chemical compound O.[Sn].[Sb] SKRWFPLZQAAQSU-UHFFFAOYSA-N 0.000 claims description 6
- 239000011135 tin Substances 0.000 claims description 6
- 229910052718 tin Inorganic materials 0.000 claims description 6
- 229920001609 Poly(3,4-ethylenedioxythiophene) Polymers 0.000 claims description 5
- 229910052751 metal Inorganic materials 0.000 claims description 5
- 239000002184 metal Substances 0.000 claims description 5
- 229920000620 organic polymer Polymers 0.000 claims description 5
- 239000000049 pigment Substances 0.000 claims description 5
- 229920000058 polyacrylate Polymers 0.000 claims description 5
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 5
- 239000004800 polyvinyl chloride Substances 0.000 claims description 5
- 230000008569 process Effects 0.000 claims description 5
- 239000004094 surface-active agent Substances 0.000 claims description 5
- 229920002994 synthetic fiber Polymers 0.000 claims description 5
- 239000012209 synthetic fiber Substances 0.000 claims description 5
- 229910052725 zinc Inorganic materials 0.000 claims description 5
- 239000011701 zinc Substances 0.000 claims description 5
- 239000004952 Polyamide Substances 0.000 claims description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 4
- 125000000129 anionic group Chemical group 0.000 claims description 4
- 229910052787 antimony Inorganic materials 0.000 claims description 4
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 claims description 4
- BFMKFCLXZSUVPI-UHFFFAOYSA-N ethyl but-3-enoate Chemical compound CCOC(=O)CC=C BFMKFCLXZSUVPI-UHFFFAOYSA-N 0.000 claims description 4
- 229910052732 germanium Inorganic materials 0.000 claims description 4
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 claims description 4
- 239000012948 isocyanate Substances 0.000 claims description 4
- 150000002513 isocyanates Chemical class 0.000 claims description 4
- 229920002647 polyamide Polymers 0.000 claims description 4
- 229920000728 polyester Polymers 0.000 claims description 4
- 229920001296 polysiloxane Polymers 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- 229920000742 Cotton Polymers 0.000 claims description 3
- 239000004971 Cross linker Substances 0.000 claims description 3
- 229920002334 Spandex Polymers 0.000 claims description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 3
- 239000000654 additive Substances 0.000 claims description 3
- 239000003945 anionic surfactant Substances 0.000 claims description 3
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical class C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 125000002091 cationic group Chemical group 0.000 claims description 3
- 239000003093 cationic surfactant Substances 0.000 claims description 3
- JAONJTDQXUSBGG-UHFFFAOYSA-N dialuminum;dizinc;oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Al+3].[Al+3].[Zn+2].[Zn+2] JAONJTDQXUSBGG-UHFFFAOYSA-N 0.000 claims description 3
- 229910052731 fluorine Inorganic materials 0.000 claims description 3
- 239000011737 fluorine Substances 0.000 claims description 3
- 239000003365 glass fiber Substances 0.000 claims description 3
- 230000004048 modification Effects 0.000 claims description 3
- 238000012986 modification Methods 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- 239000002736 nonionic surfactant Substances 0.000 claims description 3
- 239000003960 organic solvent Substances 0.000 claims description 3
- 229920001467 poly(styrenesulfonates) Polymers 0.000 claims description 3
- 229920000647 polyepoxide Polymers 0.000 claims description 3
- 239000004645 polyester resin Substances 0.000 claims description 3
- 229920001225 polyester resin Polymers 0.000 claims description 3
- 229910052710 silicon Inorganic materials 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- 229920003048 styrene butadiene rubber Polymers 0.000 claims description 3
- 239000010936 titanium Substances 0.000 claims description 3
- 229910052719 titanium Inorganic materials 0.000 claims description 3
- 229920002748 Basalt fiber Polymers 0.000 claims description 2
- 229920000049 Carbon (fiber) Polymers 0.000 claims description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 2
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 claims description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 2
- 229920000877 Melamine resin Polymers 0.000 claims description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 2
- 239000004962 Polyamide-imide Substances 0.000 claims description 2
- 239000004698 Polyethylene Substances 0.000 claims description 2
- 239000004642 Polyimide Substances 0.000 claims description 2
- 229920000265 Polyparaphenylene Polymers 0.000 claims description 2
- 239000004734 Polyphenylene sulfide Substances 0.000 claims description 2
- 239000004743 Polypropylene Substances 0.000 claims description 2
- 229920001807 Urea-formaldehyde Polymers 0.000 claims description 2
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims description 2
- 239000000853 adhesive Substances 0.000 claims description 2
- 230000001070 adhesive effect Effects 0.000 claims description 2
- 239000004760 aramid Substances 0.000 claims description 2
- 229920003235 aromatic polyamide Polymers 0.000 claims description 2
- 229910052785 arsenic Inorganic materials 0.000 claims description 2
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 claims description 2
- 229910052797 bismuth Inorganic materials 0.000 claims description 2
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 claims description 2
- 239000004917 carbon fiber Substances 0.000 claims description 2
- 229910052804 chromium Inorganic materials 0.000 claims description 2
- 239000011651 chromium Substances 0.000 claims description 2
- 239000002131 composite material Substances 0.000 claims description 2
- 238000004043 dyeing Methods 0.000 claims description 2
- 239000003822 epoxy resin Substances 0.000 claims description 2
- 229910052733 gallium Inorganic materials 0.000 claims description 2
- 229910052749 magnesium Inorganic materials 0.000 claims description 2
- 239000011777 magnesium Substances 0.000 claims description 2
- PNHVEGMHOXTHMW-UHFFFAOYSA-N magnesium;zinc;oxygen(2-) Chemical compound [O-2].[O-2].[Mg+2].[Zn+2] PNHVEGMHOXTHMW-UHFFFAOYSA-N 0.000 claims description 2
- 150000002739 metals Chemical class 0.000 claims description 2
- 239000002557 mineral fiber Substances 0.000 claims description 2
- 229910052698 phosphorus Inorganic materials 0.000 claims description 2
- 239000011574 phosphorus Substances 0.000 claims description 2
- 239000004014 plasticizer Substances 0.000 claims description 2
- 229920000747 poly(lactic acid) Polymers 0.000 claims description 2
- 229920002239 polyacrylonitrile Polymers 0.000 claims description 2
- 229920002312 polyamide-imide Polymers 0.000 claims description 2
- 229920000573 polyethylene Polymers 0.000 claims description 2
- 229920001721 polyimide Polymers 0.000 claims description 2
- 239000004626 polylactic acid Substances 0.000 claims description 2
- 229920000069 polyphenylene sulfide Polymers 0.000 claims description 2
- 229920001155 polypropylene Polymers 0.000 claims description 2
- 229920000128 polypyrrole Polymers 0.000 claims description 2
- 229920001343 polytetrafluoroethylene Polymers 0.000 claims description 2
- 239000004810 polytetrafluoroethylene Substances 0.000 claims description 2
- 229920000123 polythiophene Polymers 0.000 claims description 2
- 229920005989 resin Polymers 0.000 claims description 2
- 239000011347 resin Substances 0.000 claims description 2
- 239000010703 silicon Substances 0.000 claims description 2
- 239000007921 spray Substances 0.000 claims description 2
- 229910052716 thallium Inorganic materials 0.000 claims description 2
- BKVIYDNLLOSFOA-UHFFFAOYSA-N thallium Chemical compound [Tl] BKVIYDNLLOSFOA-UHFFFAOYSA-N 0.000 claims description 2
- 239000002562 thickening agent Substances 0.000 claims description 2
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 claims description 2
- 229910001887 tin oxide Inorganic materials 0.000 claims description 2
- 229920002554 vinyl polymer Polymers 0.000 claims description 2
- 210000002268 wool Anatomy 0.000 claims description 2
- 229920003043 Cellulose fiber Polymers 0.000 claims 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 1
- 239000004890 Hydrophobing Agent Substances 0.000 claims 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims 1
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 claims 1
- 239000003139 biocide Substances 0.000 claims 1
- 239000003431 cross linking reagent Substances 0.000 claims 1
- 239000000417 fungicide Substances 0.000 claims 1
- 239000002243 precursor Substances 0.000 claims 1
- 239000004627 regenerated cellulose Substances 0.000 claims 1
- 239000012748 slip agent Substances 0.000 claims 1
- 230000000694 effects Effects 0.000 abstract description 11
- 230000005670 electromagnetic radiation Effects 0.000 abstract description 5
- 238000010438 heat treatment Methods 0.000 abstract 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 73
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 21
- 229920001228 polyisocyanate Polymers 0.000 description 20
- 239000005056 polyisocyanate Substances 0.000 description 20
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 18
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 12
- 239000000463 material Substances 0.000 description 11
- 230000005855 radiation Effects 0.000 description 11
- 230000009102 absorption Effects 0.000 description 9
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 9
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 9
- 229920001223 polyethylene glycol Polymers 0.000 description 9
- 238000002360 preparation method Methods 0.000 description 8
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 7
- 239000002202 Polyethylene glycol Substances 0.000 description 7
- 239000006185 dispersion Substances 0.000 description 7
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 238000013459 approach Methods 0.000 description 5
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical group O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 5
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 5
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 5
- 239000008234 soft water Substances 0.000 description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 4
- 239000011358 absorbing material Substances 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 230000008859 change Effects 0.000 description 4
- 229920001940 conductive polymer Polymers 0.000 description 4
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 4
- 230000003287 optical effect Effects 0.000 description 4
- 229920001451 polypropylene glycol Polymers 0.000 description 4
- RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 description 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
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 3
- 230000002411 adverse Effects 0.000 description 3
- 238000009833 condensation Methods 0.000 description 3
- 230000005494 condensation Effects 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 238000004132 cross linking Methods 0.000 description 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical group OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 150000003254 radicals Chemical class 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 2
- LFSYUSUFCBOHGU-UHFFFAOYSA-N 1-isocyanato-2-[(4-isocyanatophenyl)methyl]benzene Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=CC=C1N=C=O LFSYUSUFCBOHGU-UHFFFAOYSA-N 0.000 description 2
- ICLCCFKUSALICQ-UHFFFAOYSA-N 1-isocyanato-4-(4-isocyanato-3-methylphenyl)-2-methylbenzene Chemical compound C1=C(N=C=O)C(C)=CC(C=2C=C(C)C(N=C=O)=CC=2)=C1 ICLCCFKUSALICQ-UHFFFAOYSA-N 0.000 description 2
- INQDDHNZXOAFFD-UHFFFAOYSA-N 2-[2-(2-prop-2-enoyloxyethoxy)ethoxy]ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOCCOC(=O)C=C INQDDHNZXOAFFD-UHFFFAOYSA-N 0.000 description 2
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- CYUZOYPRAQASLN-UHFFFAOYSA-N 3-prop-2-enoyloxypropanoic acid Chemical compound OC(=O)CCOC(=O)C=C CYUZOYPRAQASLN-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000002841 Lewis acid Substances 0.000 description 2
- 229920000433 Lyocell Polymers 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 150000001241 acetals Chemical class 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 125000005024 alkenyl aryl group Chemical group 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 125000002877 alkyl aryl group Chemical group 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 150000004056 anthraquinones Chemical class 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 125000005018 aryl alkenyl group Chemical group 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- PMHQVHHXPFUNSP-UHFFFAOYSA-M copper(1+);methylsulfanylmethane;bromide Chemical compound Br[Cu].CSC PMHQVHHXPFUNSP-UHFFFAOYSA-M 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- DYDNPESBYVVLBO-UHFFFAOYSA-N formanilide Chemical compound O=CNC1=CC=CC=C1 DYDNPESBYVVLBO-UHFFFAOYSA-N 0.000 description 2
- 125000005842 heteroatom Chemical group 0.000 description 2
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 150000007517 lewis acids Chemical class 0.000 description 2
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 235000011007 phosphoric acid Nutrition 0.000 description 2
- KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 description 2
- 235000019260 propionic acid Nutrition 0.000 description 2
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical group O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 2
- 239000013074 reference sample Substances 0.000 description 2
- 239000000523 sample Substances 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000001384 succinic acid Substances 0.000 description 2
- 230000002195 synergetic effect Effects 0.000 description 2
- 229920001897 terpolymer Polymers 0.000 description 2
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- 239000011572 manganese Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000001404 mediated effect Effects 0.000 description 1
- 238000002074 melt spinning Methods 0.000 description 1
- 238000010327 methods by industry Methods 0.000 description 1
- YDKNBNOOCSNPNS-UHFFFAOYSA-N methyl 1,3-benzoxazole-2-carboxylate Chemical compound C1=CC=C2OC(C(=O)OC)=NC2=C1 YDKNBNOOCSNPNS-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- RJMRIDVWCWSWFR-UHFFFAOYSA-N methyl(tripropoxy)silane Chemical compound CCCO[Si](C)(OCCC)OCCC RJMRIDVWCWSWFR-UHFFFAOYSA-N 0.000 description 1
- LUCXVPAZUDVVBT-UHFFFAOYSA-N methyl-[3-(2-methylphenoxy)-3-phenylpropyl]azanium;chloride Chemical compound Cl.C=1C=CC=CC=1C(CCNC)OC1=CC=CC=C1C LUCXVPAZUDVVBT-UHFFFAOYSA-N 0.000 description 1
- HLXDKGBELJJMHR-UHFFFAOYSA-N methyl-tri(propan-2-yloxy)silane Chemical compound CC(C)O[Si](C)(OC(C)C)OC(C)C HLXDKGBELJJMHR-UHFFFAOYSA-N 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical compound CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- INJVFBCDVXYHGQ-UHFFFAOYSA-N n'-(3-triethoxysilylpropyl)ethane-1,2-diamine Chemical compound CCO[Si](OCC)(OCC)CCCNCCN INJVFBCDVXYHGQ-UHFFFAOYSA-N 0.000 description 1
- PHQOGHDTIVQXHL-UHFFFAOYSA-N n'-(3-trimethoxysilylpropyl)ethane-1,2-diamine Chemical compound CO[Si](OC)(OC)CCCNCCN PHQOGHDTIVQXHL-UHFFFAOYSA-N 0.000 description 1
- NHBRUUFBSBSTHM-UHFFFAOYSA-N n'-[2-(3-trimethoxysilylpropylamino)ethyl]ethane-1,2-diamine Chemical compound CO[Si](OC)(OC)CCCNCCNCCN NHBRUUFBSBSTHM-UHFFFAOYSA-N 0.000 description 1
- YLBPOJLDZXHVRR-UHFFFAOYSA-N n'-[3-[diethoxy(methyl)silyl]propyl]ethane-1,2-diamine Chemical compound CCO[Si](C)(OCC)CCCNCCN YLBPOJLDZXHVRR-UHFFFAOYSA-N 0.000 description 1
- MQWFLKHKWJMCEN-UHFFFAOYSA-N n'-[3-[dimethoxy(methyl)silyl]propyl]ethane-1,2-diamine Chemical compound CO[Si](C)(OC)CCCNCCN MQWFLKHKWJMCEN-UHFFFAOYSA-N 0.000 description 1
- KFOZMMAXUUCIKU-UHFFFAOYSA-N n-(3-triethoxysilylpropyl)butan-1-amine Chemical compound CCCCNCCC[Si](OCC)(OCC)OCC KFOZMMAXUUCIKU-UHFFFAOYSA-N 0.000 description 1
- XCOASYLMDUQBHW-UHFFFAOYSA-N n-(3-trimethoxysilylpropyl)butan-1-amine Chemical compound CCCCNCCC[Si](OC)(OC)OC XCOASYLMDUQBHW-UHFFFAOYSA-N 0.000 description 1
- LSWADWIFYOAQRZ-UHFFFAOYSA-N n-(ethoxymethyl)prop-2-enamide Chemical compound CCOCNC(=O)C=C LSWADWIFYOAQRZ-UHFFFAOYSA-N 0.000 description 1
- ULYOZOPEFCQZHH-UHFFFAOYSA-N n-(methoxymethyl)prop-2-enamide Chemical class COCNC(=O)C=C ULYOZOPEFCQZHH-UHFFFAOYSA-N 0.000 description 1
- YPHQUSNPXDGUHL-UHFFFAOYSA-N n-methylprop-2-enamide Chemical compound CNC(=O)C=C YPHQUSNPXDGUHL-UHFFFAOYSA-N 0.000 description 1
- 239000002105 nanoparticle Substances 0.000 description 1
- 150000002791 naphthoquinones Chemical class 0.000 description 1
- 230000004297 night vision Effects 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- VVRQVWSVLMGPRN-UHFFFAOYSA-N oxotungsten Chemical class [W]=O VVRQVWSVLMGPRN-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- YOTGRUGZMVCBLS-UHFFFAOYSA-N pentadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCOC(=O)C(C)=C YOTGRUGZMVCBLS-UHFFFAOYSA-N 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical class O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920006389 polyphenyl polymer Polymers 0.000 description 1
- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 229920005650 polypropylene glycol diacrylate Polymers 0.000 description 1
- 238000012673 precipitation polymerization Methods 0.000 description 1
- WWBMGKDLVQBYLQ-UHFFFAOYSA-N prop-2-ene-1,1,1-tricarboxylic acid Chemical compound OC(=O)C(C=C)(C(O)=O)C(O)=O WWBMGKDLVQBYLQ-UHFFFAOYSA-N 0.000 description 1
- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 1
- MILWSGRFEGYSGM-UHFFFAOYSA-N propane-1,2-diol;propane-1,2,3-triol Chemical compound CC(O)CO.OCC(O)CO MILWSGRFEGYSGM-UHFFFAOYSA-N 0.000 description 1
- 239000003586 protic polar solvent Substances 0.000 description 1
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 150000003377 silicon compounds Chemical class 0.000 description 1
- 125000005373 siloxane group Chemical group [SiH2](O*)* 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- OQTSOKXAWXRIAC-UHFFFAOYSA-N tetrabutan-2-yl silicate Chemical compound CCC(C)O[Si](OC(C)CC)(OC(C)CC)OC(C)CC OQTSOKXAWXRIAC-UHFFFAOYSA-N 0.000 description 1
- UQMOLLPKNHFRAC-UHFFFAOYSA-N tetrabutyl silicate Chemical compound CCCCO[Si](OCCCC)(OCCCC)OCCCC UQMOLLPKNHFRAC-UHFFFAOYSA-N 0.000 description 1
- UWHCKJMYHZGTIT-UHFFFAOYSA-N tetraethylene glycol Chemical compound OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
- LFQCEHFDDXELDD-UHFFFAOYSA-N tetramethyl orthosilicate Chemical compound CO[Si](OC)(OC)OC LFQCEHFDDXELDD-UHFFFAOYSA-N 0.000 description 1
- ZUEKXCXHTXJYAR-UHFFFAOYSA-N tetrapropan-2-yl silicate Chemical compound CC(C)O[Si](OC(C)C)(OC(C)C)OC(C)C ZUEKXCXHTXJYAR-UHFFFAOYSA-N 0.000 description 1
- ZQZCOBSUOFHDEE-UHFFFAOYSA-N tetrapropyl silicate Chemical compound CCCO[Si](OCCC)(OCCC)OCCC ZQZCOBSUOFHDEE-UHFFFAOYSA-N 0.000 description 1
- BCLLLHFGVQKVKL-UHFFFAOYSA-N tetratert-butyl silicate Chemical compound CC(C)(C)O[Si](OC(C)(C)C)(OC(C)(C)C)OC(C)(C)C BCLLLHFGVQKVKL-UHFFFAOYSA-N 0.000 description 1
- 238000009988 textile finishing Methods 0.000 description 1
- 150000003608 titanium Chemical class 0.000 description 1
- 229910052613 tourmaline Inorganic materials 0.000 description 1
- 229940070527 tourmaline Drugs 0.000 description 1
- 239000011032 tourmaline Substances 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- IZRJPHXTEXTLHY-UHFFFAOYSA-N triethoxy(2-triethoxysilylethyl)silane Chemical compound CCO[Si](OCC)(OCC)CC[Si](OCC)(OCC)OCC IZRJPHXTEXTLHY-UHFFFAOYSA-N 0.000 description 1
- DENFJSAFJTVPJR-UHFFFAOYSA-N triethoxy(ethyl)silane Chemical compound CCO[Si](CC)(OCC)OCC DENFJSAFJTVPJR-UHFFFAOYSA-N 0.000 description 1
- CPUDPFPXCZDNGI-UHFFFAOYSA-N triethoxy(methyl)silane Chemical compound CCO[Si](C)(OCC)OCC CPUDPFPXCZDNGI-UHFFFAOYSA-N 0.000 description 1
- JCVQKRGIASEUKR-UHFFFAOYSA-N triethoxy(phenyl)silane Chemical compound CCO[Si](OCC)(OCC)C1=CC=CC=C1 JCVQKRGIASEUKR-UHFFFAOYSA-N 0.000 description 1
- NBXZNTLFQLUFES-UHFFFAOYSA-N triethoxy(propyl)silane Chemical compound CCC[Si](OCC)(OCC)OCC NBXZNTLFQLUFES-UHFFFAOYSA-N 0.000 description 1
- QQQSFSZALRVCSZ-UHFFFAOYSA-N triethoxysilane Chemical compound CCO[SiH](OCC)OCC QQQSFSZALRVCSZ-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- ZNOCGWVLWPVKAO-UHFFFAOYSA-N trimethoxy(phenyl)silane Chemical compound CO[Si](OC)(OC)C1=CC=CC=C1 ZNOCGWVLWPVKAO-UHFFFAOYSA-N 0.000 description 1
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
- YUYCVXFAYWRXLS-UHFFFAOYSA-N trimethoxysilane Chemical compound CO[SiH](OC)OC YUYCVXFAYWRXLS-UHFFFAOYSA-N 0.000 description 1
- 229940096522 trimethylolpropane triacrylate Drugs 0.000 description 1
- 229920006305 unsaturated polyester Polymers 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
Definitions
- the present invention describes a textile auxiliary which achieves a locally warming effect on energy-absorbing surfaces of electromagnetic radiation and / or on reduced energy output on textile surfaces, woven fabrics, laid fabrics, knitted fabrics, nonwovens and knitted fabrics or products made therefrom.
- EP 1 792 724 A2 describes two-sided coating with a tourmaline tape in order to reduce the emission of material from the body of the wearer wearing the clothing. This approach requires a special apparatus described in the patent and such textiles have undesirable color changes and haptic changes.
- EP 1 847 635 A1 describes the use of IR-reflecting pigments based on activated tungsten oxides.
- Organic bisiminium compounds are used in Japanese Patent Application JP 2009203596 to produce IR absorbing textiles.
- these approaches are unsuitable for producing colorless or light-colored textiles.
- IR-absorbing dyes based on conductive organic polymers are used on textiles in order to reduce the emitting heat radiation and thus the detectability by night vision devices.
- Benzoxazoline-based UV absorbers are incorporated with transparent conductive oxides in polyester fibers by melt-spinning processes. Thus the authors achieve an improvement of the Thermal insulation.
- Japanese patent JP 2004149931 describes the use of zirconium carbide, titanium oxide or special metal complexes as IR radiation absorbing compounds for the use of underwear.
- WO 01/25367 A1 describes the preparation of such oxides by the hydrothermal route and the use thereof to produce textiles with sensor properties or antistatic effects.
- EP 0 341 554 A1 large quantities of such oxides are added to synthetic fibers in a masterbatch application in order to produce conductive textiles.
- TW 201113410 uses indium tin oxide in combination with titanium oxide layers. In none of these writings is the heat retention of textbooks corresponding to processed textiles.
- Such ternary oxides have a graying or generally a clearly color-changing effect as a textile auxiliaries.
- Methods for lowering remission or reflection are used primarily for camouflage purposes in the military sector. Above all, the radiation ranges of the infrared light are influenced.
- DE 10 258 014 A1 describes a method for introducing glass fibers coated on one side with aluminum powder in heat-treated blankets, in order to enable visible-optical camouflage by reducing the emitted thermal radiation.
- the reflective layers are directed towards the heat source.
- Another commonly described method for influencing the reflection and / or remission is the selection of suitable colorants. Reduction of the remission of textiles is reported in, for example, RU 2196855 and PL 202000. By the method described therein, however, can only produce colored textiles.
- DE 10 2009 006 832 A1 describes a liquid or semi-solid formulation of spectrally selective particles for coating flexible bodies.
- the coating is characterized by having a significantly lower thermal emissivity at room temperature than the uncoated body, while maintaining the body's texture / texture and flexibility.
- the coatings can be given a virtually arbitrary color impression, while maintaining a lowered emissivity.
- EP 1 321 291 A1 and EP 1 437 438 A1 describe textile auxiliaries for IR absorption and / or reflection and the use of the semiconductors indium tin oxide and antimony tin oxide.
- WO 2008/004993 A2 describes layers with absorptions in the near infrared range as well as corresponding articles containing these layers. This should not change the visual impression of the entire article.
- non-color-modifying electromagnetic radiation absorbing layers can be applied permanently and wash-permanently on textiles, whereby textiles under IR or solar radiation absorb an increased amount of heat and / or deliver a reduced amount of heat. It has been found, particularly surprisingly, that the described effect can be synergistically enhanced by the selection of suitable binder polymers.
- the invention in a first embodiment, a textile auxiliary for IR absorption and / or reflection of textiles, containing
- binder polymers from the group of polyurethanes, polyacrylates, styrene-butadienes, silicones, siloxanes, sol gels, polyvinyl chloride, ethylvinyl acetate, epoxy or polyester resins,
- (C) surfactants selected from the group of anionic, cationic or nonionic surfactants and
- the present invention combines the simplicity of already existing textile-technological processes such as equipment by pad-forced application, coating by means of pastes or foams, spray application, printing, dipping and exhausting process and single filament application on Galette or in the dip bath with an effect of increased heat energy absorption or reduced heat emission (-. loss) of such finished textiles by selecting suitable compounds.
- textile parameters such as hand and tear are not adversely affected.
- the color of a textile is not adversely affected.
- white or colorless textiles can be refined with this invention.
- such a finished textile under the influence of electromagnetic radiation heats significantly more than a corresponding comparison pattern of the same parameters (eg material composition, color, weight, thickness, structure and weaving). At the same time this can be a reduction of the remission Electromagnetic radiation and / or increase the absorption thereof.
- the first group a) includes the compounds of the A m B v type semiconductor (see AF Holleman, E. Wiberg, Lehrbuch der anorganischen Chemie, 101st ed., De Gruyter, Berlin, pp. 1098-1100).
- Suitable elementary semiconductors of group b) are suitable modifications of tin, indium, carbon, silicon and germanium.
- the group d) of the oxide semiconductor includes conductive transparent oxides.
- the A m B v -Halbleiter type of the group in the context of this invention comprises the compounds AB of the elements A, wherein A for aluminum, gallium, indium, thallium, germanium, tin, lead and B for nitrogen, phosphorus, arsenic, antimony and Bismuth in any stoichiometric ratios.
- Particularly preferred within the meaning of the invention are the binary pentel compounds of aluminum, in particular aluminum nitride, since they are generally distinguished by high chemical inertness.
- organic conductive polymers such as polypyrrole, polyaniline, polyparaphenylene, polythiophene, poly (4,4-dioctylcyclopentadithiophene), poly (3,4-ethylenedioxythiophene) or Poly (3,4-ethylenedioxythiophene) / poly (styrenesulfonate) as a semiconductor alone or in combination with other suitable conductive polymers solve the technical problem.
- This group includes, for example, fluorine doped tin oxide, indium tin oxide, antimony tin oxide, aluminum zinc oxide, magnesium zinc oxide, chromium titanium oxide.
- the transparent conductive oxides can particularly preferably be used in combination with suitable polymers in the preparation.
- the semiconductors are selected from at least one of the semiconductors of groups a), b) and c) and furthermore at least one semiconductor from group d), or mixtures of at least two semiconductors selected from groups a), b) and c), in particular at least one from group a) and at least one from group c) or at least two semiconductors from group d).
- infrared radiation-absorbing dyes may optionally be additionally contained in small amounts in order to increase the effect of heat absorption.
- Such infrared radiation absorbing materials according to the invention can be either organic or inorganic as defined above.
- infrared radiation-absorbing materials in the sense of the invention are materials which have a wavelength range of 700 to 35,000 nm at at least two of the wavelengths 1000 nm, 1500 nm, 2000 nm and 3500 nm have a molar extinction coefficient of at least 1.5 l mol.cm -1 .
- the infrared radiation absorbing material has an absorption maximum in a range from 900 to
- a material selected from the group consisting of phthalocyanines, naphthalocyanines, anthraquinones, cyanine compounds, squalylium compounds, thiolnickel oxides is used as organic infrared radiation absorbing material.
- the particulate semiconductors used in this invention have a particle size (number average, d 5 o, laser diffraction) of 1 nm to 10 ⁇ , preferably less than 2 ⁇ on.
- the use of one or more of the abovementioned semiconductors from the abovementioned groups a), b), c) or d) solves the technical problem.
- the effect can be synergistically enhanced by infrared-absorbing organic dyes.
- Suitable binder polymers for the semiconductors are, for example, homopolymers, copolymers or terpolymers based on polyacrylates, polyurethanes, styrene-butadienes, sol-gels, silicones, epoxide resins, polyvinyl chloride, ethylvinyl acetate, polyester resins or mixtures of these classes in the invention.
- Cross-linked, cross-linking or reactive systems are preferred for the purposes of the invention, particularly preferably those whose films show a glass transition state of less than 0 ° C.
- Suitable starting components for the polyurethanes of the invention are aliphatic, cycloaliphatic, araliphatic, aromatic and heterocyclic polyisocyanates, such as those described by W. Siefken in Justus Liebigs Annalen der Chemie, 562, pages 75 to 136, for example those of the formula
- Q is an aliphatic hydrocarbon radical having 2 to 18, preferably 6 to 10 C atoms, a cycloaliphatic hydrocarbon radical having 4 to 15, preferably 5 to 10 C atoms, an aromatic hydrocarbon radical with 6 to 15, preferably 6 to 13 C atoms, or an aliphatic hydrocarbon radical having 8 to 15, preferably 8 to 13 C atoms, for example Ethylene diisocyanate, 1,4-tetramethylene diisocyanate, 1,6-
- HDI Hexamethylene diisocyanate
- 1,12-dodecane diisocyanate 1,12-dodecane diisocyanate
- cyclobutane 1,12-dodecane diisocyanate
- 1,3-diisocyanate, cyclohexane-1,3- and 1,4-diisocyanate and any mixtures of these isomers 1-isocyanato-3,3,5-tri-methyl-5-isocyanatomethyl-cyclohexane, 2,4- and 2, 6-Hexahydrotoluylendiisocyanat and any mixtures of these isomers, hexahydro-1,3- and -1,4-phenylene diisocyanate, perhydro-2,4'- and -4,4'-diphenyl-methane diisocyanate, 1,3- and 1,4-phenylene diisocyanate, 1,4-diol diisocyanate (DDI), 4,4'-stilbenediisocyanate, 3,3'-dimethyl-4,4'-biphenylene diisocyanate (TODI)
- TDI 2,4- and 2,6-toluene diisocyanate
- MDI diphenylmethane-2,4'- and / or -4,4'-diisocyanate
- NDI naphthylene-l, 5-diisocyanate
- triphenylmethane-4,4 ', 4 "- triisocyanate polyphenyl-polymethylene-polyisocyanates, as obtained by aniline-formaldehyde condensation and subsequent phosgenation and, for example, in GB-PS 874 430 and GB-PS 848,671 described, m- and p-Isocyanatophenylsulfonylisocyanate according to US Patent 3,454,606, perchlorinated aryl polyisocyanates, as described in US-PS 3,277,138, carbodiimide-containing polyisocyanates, as described in US-PS 3,152,162 and in DE-OS 25 04 400, 25 37 685 and 25 52 350, norbornane diisocyanates according to US Pat.
- polyisocyanates for example the 2,4- and 2,6-toluene diisocyanate and any mixtures of these isomers (“TDI”), 4,4'-diphenylmethane diisocyanate, 2,4'-diphenylmethane diisocyanate, 2,2 ' Diphenylmethane diisocyanate and polyphenyl polymethylene polyisocyanate, as prepared by aniline-formaldehyde condensation and subsequent phosgenation (“crude MDI”), and carbodiimide groups, uretonimine groups, urethane groups,
- Allophanate groups, isocyanurate groups, urea groups or biuret polyisocyanates ("modified Polyisocyanates "), in particular those modified polyisocyanates which are derived from 2,4- and / or 2,6-toluene diisocyanate or from 4,4'- and / or 2,4'-diphenylmethane diisocyanate. Also suitable are naphthylene-1, 5-diisocyanate and mixtures of said polyisocyanates.
- Polyacrylates in the context of the present invention are in particular prepared by solution, precipitation, emulsion or inverse emulsion polymerization.
- Acrylates are preferably selected from the group consisting of 1,4-butanediol di (meth) acrylate, 1,6-hexanediol di (meth) acrylate, neopentyl glycol di (meth) acrylate, polyethylene glycol di (meth) acrylate, neopentyl glycol adipate di ( meth) acrylate, neopentyl glycol hydroxypivalate di (meth) acrylate, dicyclopentanyl di (meth) acrylate, dicyclopentenyl di (meth) acrylate modified with caprolactam, phosphoric di (meth) acrylate modified with ethylene oxide, cyclohexyl di (meth) acrylate modified with an allyl group , Isocyanurate di (meth) acrylate, trimethylolpropane tri (meth) acrylate, dipentaerythritol tri (meth) acrylate,
- eth) acrylate such as methyl (meth) acrylate, ethyl (meth) acrylate, isopropyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, butyl (meth) acrylate, cyclohexyl (meth) acrylate, tetrahydrofurfuryl (meth) acrylate, 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, polyethylene glycol mono (meth) acrylate, Methoxypolyethylene glycol mono (meth) acrylate, polypropylene glycol mono (meth) acrylate, polyethylene glycol polypropylene glycol mono (meth) acrylate, polyethylene glycol polytetramethylene glycol mono (meth) acrylate and glycidyl (meth) acrylate; difunctional (meth) acrylate, such as ethylene glycol di (meth)
- sol-gel binder polymers for example, the following silicon compounds or mixtures thereof can be used, which are selected from the group tetramethoxysilane, tetraethoxysilane, tetra-n-propoxysilane,
- alkylene- or arylene-bridged di-esters are oligosilanes such as 1,2-bis (triethoxysilyl) ethane, l, 2-bis (trimethoxysilyl) ethane, l, 4-phenylenebis (triethoxysilane), l, 4-phenylenebis (trimethoxysilane).
- aluminum salts, aluminum alcoholates, zinc salts, zinc alcoholates, zirconium salts, zirconium salts, zirconium alcoholates, titanium salts, titanium alcoholates, iron salts, iron alcoholates, manganese salts or manganese alkoxides can be used as starting materials of the systems.
- the binder is preferably prepared in water and / or organic solvents, optionally with the aid of dispersants, in particular in mono-, oligo- or polyfunctional alcohols, particularly preferably in aqueous solutions of the abovementioned alcohols.
- the crosslinking by hydrolysis of the building blocks and subsequent condensation of the hydrolyzed starting materials is by mineral or organic acids, alkali, organic bases, transition metal catalysts such as titanates and / or zirconates and / or protic solvents, preferably water, because of safety aspects such as flammability and environmental aspects is advantageous, mediated and the binder is obtained as a colloidal solution or dispersion.
- Silicone binder polymers usually consist of the repeating unit dimethylsiloxane, which can be supplemented for example by equilibration reactions by other siloxane groups.
- the polymer therefore has the structure
- M and n independently assume values between 0 and 100,000.
- the base unit - (O-Si (Me) 2 ) - may be partially or completely replaced by units of the type - (O-SiRR ') -, where R and R' may be independently modified and optionally functionalized organic radicals of the alkyl, aryl, alkenyl, alkylaryl, arylalkyl, arylalkenyl, alkenylaryl, hydrogen, hydroxyl , May contain amine.
- the radicals may be attached directly to the central silicon atom or via a heteroatom such as oxygen or nitrogen.
- the silicon units are connected via a group Y or are directly bonded to each other.
- Y and Z are independently selected from the aforementioned organic groups or from the group of said heteroatoms.
- the polymer can carry in end ⁇ , ⁇ position end groups R "and / or R '" from the abovementioned groups, which can be chosen independently of one another.
- the textile auxiliaries according to the invention can be present as solutions or dispersions in water and / or an organic solvent. Particularly preferred in this invention are aqueous solutions or dispersions of the components, since this is advantageous for process engineering and environmental aspects.
- surface-active substances from the group of anionic, cationic or nonionic surfactants are used.
- anionic or nonionic, particularly preferably nonionic, surfactants are particularly preferred.
- further dispersants such as thickeners based on Carboxyalkylpolysaccharide or polyacrylates can be used.
- the preparation on which the invention is based can be combined with other conventional textile auxiliaries and applied together in standard textile processes.
- the textile auxiliaries thus obtained can be used as fleets, foams or pastes for textile finishing. Also, the combination of these additives and the aforementioned components to a preparation according to the invention.
- fixers and / or cross-linkers from the group of blocked and unblocked isocyanates, melamine-formaldehyde resins, urea-formaldehyde resins and / or di-, oligo- or polycarboxylic acids, if appropriate in combination with suitable catalysts, are preferably used in the context of the invention. which increase the reactivity and / or selectivity of the crosslinking used.
- W is an organic radical from the group of optionally functionalized alkyl, aryl, alkenyl, alkylaryl, arylalkyl, arylalkenyl, alkenylaryl, m is a number either 0 or 1 and n is a number between 2 and 100000 covers.
- Alkanedicarboxylic acids are particularly preferred, in particular malonic acid, maleic acid, derivatives succinic and oxalic acid.
- oligo- and polycarboxylic acids are alkyloligo-, alkylpoly- or aryloligocarboxylic acids, particular preference is given to butanetetracarboxylic acid, all-cis-1,2,3,4-cyclopentanetetracarboxylic acid, tricarballylic acid, citric acid, 1,2,3-trans-carboxylic acid.
- Propentricarboxylic acid, succinic acid and derivatives of polyacrylic acid and polymethacrylic acid as homopolymers or copolymers.
- Suitable catalysts for the fixers are generally Lewis acids or bases.
- Magnesium chloride is particularly preferably used alone or in combination with Bronsted acids, preferably orthophosphoric acid, citric acid, sulfuric acid.
- Bronsted acids preferably orthophosphoric acid, citric acid, sulfuric acid.
- Brönsted acids preferably ortho-phosphoric acid, citric acid, sulfuric acid without Lewis acid can be used.
- basic catalysts such as amines, hypophosphites, phosphonates, pyro and polyphosphates or alkali.
- the textile material according to the invention may be composed of natural fibers such as cotton, bast fibers, hard fibers, wool, silk, mineral fibers and / or synthetic fibers such as cellulose regenerated fibers, polylactic acid, polyester, polyamide, polyimide, polyamideimide, polyphenylene sulfide, aramid, polyvinyl chloride, polyacrylonitrile, Polyvinyl acetal, polytetrafluoroethylene, polyethylene, polypropylene, polyurethane, elastane, carbon fibers, silicate fibers, glass fibers, basalt fibers, metal fibers consist, contain these or consist of mixtures of the materials mentioned. Also, laminated fibers or fibers cast in a composite material are according to the invention. The color change of the textile after treatment with the textile auxiliaries according to the invention, measured in the CIE-Lab color space, is very small.
- the textile according to the invention shows a color change of less than or equal to 10, preferably less than 3, units according to CIE-Lab color space or a maximum degree of whiteness of less than or equal to 6, preferably less than or equal to 3, Berger units.
- the textile auxiliaries according to the invention is characterized in particular in that a product refined therewith exhibits a lower remission and / or a higher absorption in the range of the infrared light and / or the solar spectrum or parts thereof.
- the textile according to the invention shows, under irradiation in the measuring apparatus according to FIG. 1, a temperature increase of 5 ° C., preferably of 15 ° C., particularly preferably of 25 ° C., compared to a non-refined reference.
- the temperature increase of the textiles was measured as a function of the duration of irradiation, whereby a reference sample was always irradiated as a comparison (FIG. 1).
- Fig. 2 shows a remission spectrum of an embodiment compared to the reference.
- the remission was determined by standard techniques using a Datacolor type instrument, type Microflash 45, preferably at a wavelength of 980 nm.
- the remission fraction was the quotient of remission of the sample divided by the remission of the reference sample: The optical assessment was carried out in a commercial Abmusterungskabine with different light sources.
- White cotton swatches (twill, 205 g / m 2 , 20 cm x 30 cm) were set with 250 ml of a fresh finish liquor consisting of 0.45% indium tin oxide added as a 20% pigment dispersion and 5% polyurethane binder polymer in soft water to pH 5.5 with acetic acid, equipped on a laboratory pad. The contact pressure of the rolls was set to 3 bar. After finishing, the fabric was dried on a laboratory fixture frame for 2 minutes at 120 ° C and then condensed for 1 minute at 150 ° C. Subsequently, the patterns were measured with a reference pattern in the apparatus shown in Fig. 1, and remission and color numbers were determined.
- Embodiment 1 The pattern was color acceptable to the textile expert, but the amount of heat absorbed is not sufficient.
- Embodiment 1 :
- White PES / lyocell fabrics (210 g / m 2 , 20 cm x 30 cm) were coated with 250 ml of a fresh finish liquor consisting of 0.02% conductive organic polymer, 5% polyurethane binder polymer, 1% fixer and 0.5 % Kollasol CDO (surfactant, available from CHT R. Beitlich GmbH), in soft water adjusted to pH 5.5 with acetic acid, on a laboratory pad. The contact pressure of the rolls was set to 3 bar. After finishing, the fabric was dried on a laboratory fixture frame for 2 minutes at 120 ° C and then condensed for 1 minute at 150 ° C. Subsequently, the patterns were measured with a reference pattern in the apparatus shown in Fig. 1, and remission and color numbers were determined.
- a fresh finish liquor consisting of 0.02% conductive organic polymer, 5% polyurethane binder polymer, 1% fixer and 0.5 % Kollasol CDO (surfactant, available from CHT R. Beitlich GmbH
- Embodiment 2 is a diagrammatic representation of Embodiment 1:
- White PES / lyocell fabrics (210 g / m 2 , 20 cm x 30 cm) were mixed with 250 ml of a freshly prepared equipment liquor consisting of 0.2% indium tin oxide, 0.02% organically conductive polymers, 5% polyurethane. Binder polymer, 1% fixer, 0.05% Kollasol CDO, adjusted to pH 5.5 in soft water with acetic acid, equipped on a laboratory pad. The contact pressure of the rolls was set to 3 bar. After finishing, the fabric was dried on a laboratory fixture frame for 2 minutes at 120 ° C and then condensed for 1 minute at 150 ° C.
- Embodiment 3 is a diagrammatic representation of Embodiment 3
- Red polyamide samples (twill weave, 120 g / m 2 , 20 cm x 30 cm) were mixed with 250 ml of a fresh finish liquor consisting of 0.8% aluminum nitride added as a 20% pigment dispersion containing 0.1% Kollasol CDO Soft water, adjusted to pH 5.5 with acetic acid, equipped on a laboratory pad. In some examples, 0.02% conductive organic polymers were also added. The contact pressure of the rolls was set to 3 bar. After finishing, the fabric was dried on a laboratory fixture frame for 2 minutes at 120 ° C and then condensed for 1 minute at 150 ° C. Subsequently, the patterns were with a reference pattern in the apparatus shown in Fig. 1 measured and determined remission and color numbers.
- Embodiment 4 is a diagrammatic representation of Embodiment 4:
- Yellow viscose fabrics (160 g / m 2 , 20 cm x 30 cm) were coated with 250 ml of a fresh finish liquor consisting of 0.2% ternary oxide, 0.05% polyaniline, 5% polyurethane binder polymer, 1% fixer, 0.25% Kollasol CDO, adjusted to pH 5.5 in acetic acid with acetic acid, on a laboratory pad. The contact pressure of the rolls was set to 3 bar. After finishing, the fabric was dried on a laboratory fixture frame for 2 minutes at 120 ° C and then condensed for 1 minute at 150 ° C.
- Embodiment 5 is a diagrammatic representation of Embodiment 5:
- Textile samples of various materials were each equipped with 250 ml of the liquor mentioned in Example 2 consisting of indium tin oxide and poly (3,4-ethylenedioxythiophene) / poly (styrenesulfonate) and Kollasol CDO on a laboratory pad.
- the contact pressure of the rolls was set to 3 bar.
- the fabric was dried on a laboratory fixture frame for 2 minutes at 120 ° C and then condensed for 1 minute at 150 ° C. Subsequently, the samples were measured as unwashed original, after 10 domestic washes (HHW) at 40 ° C with a reference pattern in the device shown in Figure 1 and the remission determined.
- HHW domestic washes
- Embodiment 6 Yellow polyester-elastane textile samples were each equipped with 250 ml of the below-mentioned liquors on a laboratory pad. The contact pressure of the rolls was set to 3 bar. After finishing, the fabric was dried on a laboratory fixture frame for 2 minutes at 120 ° C and then condensed for 1 minute at 150 ° C. Subsequently, the patterns were measured with a reference pattern in the device shown in Figure 1 and the remission determined.
- sol-gel binder 0 ° C 101% unremarkable 2% sol-gel binder (iSys 22 ° C 81% marginal MTX), gray
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- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
Abstract
Description
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DE102012209598A DE102012209598A1 (de) | 2012-06-06 | 2012-06-06 | Textilhilfsmittel und damit veredeltes Textilprodukt |
PCT/EP2013/061500 WO2013182568A2 (de) | 2012-06-06 | 2013-06-04 | Textilhilfsmittel und damit veredeltes textilprodukt |
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EP2859145A2 true EP2859145A2 (de) | 2015-04-15 |
EP2859145B1 EP2859145B1 (de) | 2017-03-15 |
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DE (1) | DE102012209598A1 (de) |
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US10252945B2 (en) | 2012-09-26 | 2019-04-09 | Multiple Energy Technologies Llc | Bioceramic compositions |
TWI555890B (zh) * | 2013-12-18 | 2016-11-01 | 財團法人工業技術研究院 | 具有吸收紅外線功能的紗線及其紡織品 |
CN106488785B (zh) | 2014-05-05 | 2020-08-25 | 复合能源技术有限公司 | 生物陶瓷组合物及其生物调节用途 |
CN104389156A (zh) * | 2014-11-04 | 2015-03-04 | 东华大学 | 一种耐久型负载氧化锌纺织品的制备方法 |
CN113089123B (zh) * | 2021-04-21 | 2022-09-20 | 上海工程技术大学 | 碳化锆/聚吡咯-聚氨酯复合纤维及其制备方法和应用 |
Family Cites Families (53)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3277138A (en) | 1966-10-04 | Method for the chlorination of aromatic isocyanates | ||
US3001973A (en) | 1953-05-23 | 1961-09-26 | Bayer Ag | Production of cross-linked plastics |
DE1022789B (de) | 1956-09-29 | 1958-01-16 | Bayer Ag | Verfahren zur Herstellung von Schaumstoffen aus Polyoxy- und/oder Polycarboxylverbindungen und Polyisocyanaten |
DE1027394B (de) | 1956-10-22 | 1958-04-03 | Bayer Ag | Verfahren zur Herstellung von Schaumstoffen |
BE562425A (de) | 1956-11-16 | |||
DE1072385C2 (de) | 1958-06-20 | 1960-07-07 | Bayer Ag | Verfahren zur Herstellung von harzartigen, gegebenenfalls noch löslichen, beim Erwärmen Isocyanatgruppen freisetzenden Polyadditionsprodukten |
BE581667A (de) | 1958-08-15 | |||
GB889050A (en) | 1959-06-12 | 1962-02-07 | Ici Ltd | Process for the manufacture of polyurethanes |
US3152162A (en) | 1959-07-29 | 1964-10-06 | Bayer Ag | Polyisocyanate-carbodiimide adducts and process for the production thereof |
US3019731A (en) | 1960-02-19 | 1962-02-06 | Advanced Oil Tools Inc | Jet perforator for well casings |
US3245833A (en) * | 1964-04-20 | 1966-04-12 | Eastman Kodak Co | Electrically conductive coatings |
NL133051C (de) | 1960-12-05 | |||
GB994890A (en) | 1961-12-18 | 1965-06-10 | Ici Ltd | New organic polyisocyanates and their manufacture |
US3455883A (en) | 1963-01-09 | 1969-07-15 | Gen Mills Inc | Polyisocyanates and derivatives |
US3454606A (en) | 1963-11-14 | 1969-07-08 | Union Carbide Corp | Isocyanatophenylsulfonyl isocyanates |
US3124605A (en) | 1963-12-05 | 1964-03-10 | Biuret polyisocyanates | |
DE1222067B (de) | 1964-11-07 | 1966-08-04 | Bayer Ag | Verfahren zur Herstellung von einheitlichen organischen Polyisocyanaten |
DE1231688B (de) | 1965-04-17 | 1967-01-05 | Bayer Ag | Verfahren zur Herstellung von Isocyanatocarbonsaeureestern polyfunktioneller Hydroxyverbindungen |
DE1230778B (de) | 1965-05-24 | 1966-12-22 | Bayer Ag | Verfahren zur Herstellung von acylierten Harnstoffpolyisocyanaten |
US3394164A (en) | 1965-10-24 | 1968-07-23 | Upjohn Co | Stabilized methylenebis-(phenyl isocyanate) compositions |
US3492301A (en) | 1965-11-01 | 1970-01-27 | Armstrong Cork Co | 2,4,6-trisubstituted sulfonylhydrazido-s-triazines |
US3567763A (en) | 1966-01-06 | 1971-03-02 | Rohm & Haas | Ester polyisocyanates |
DE1618380C3 (de) | 1967-03-08 | 1975-09-11 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung eines bei Raumtemperatur flüssigen Diphenylmethan-diisocyanatpräparates |
DE1720747C3 (de) | 1967-11-09 | 1980-06-26 | Bayer Ag | Verfahren zur Herstellung von Iso cyanatgruppen aufweisenden Telomerisaten |
US3513491A (en) | 1968-03-13 | 1970-05-26 | Donald W Gordon | Athlete's landing pit with foam-block cushion units |
DE1929034B2 (de) | 1969-06-07 | 1972-04-20 | Farbenfabriken Bayer Ag, 5090 Lever Kusen | Verfahren zur herstellung von flammfesten urethangruppen aufweisenden schaumstoffen |
AT304874B (de) | 1969-06-20 | 1973-01-25 | Bayer Ag | Verfahren zur Herstellung von flammwidrigen, gegebenenfalls zellförmigen, Urethangruppen aufweisenden Kunststoffen |
DE2002064C2 (de) | 1970-01-17 | 1983-09-01 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von flammwidrigen elastischen oder halbelastischen Schaumstoffen |
DE2009179C3 (de) | 1970-02-27 | 1974-07-11 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von Allophanatpoly isocy anaten |
DE2504400A1 (de) | 1975-02-01 | 1976-08-05 | Bayer Ag | Lagerstabile, carbodiimidgruppen enthaltende polyisocyanate |
DE2537685C2 (de) | 1975-08-23 | 1989-04-06 | Bayer Ag, 5090 Leverkusen | Verfahren zur teilweisen Carbodiimidisierung der Isocyanatgruppen von organischen Polyisocyanaten |
DE2552350A1 (de) | 1975-11-21 | 1977-05-26 | Bayer Ag | Lagerstabile, carbodiimidgruppen enthaltende polyisocyanate |
DE2737192A1 (de) | 1976-11-10 | 1978-05-11 | Hydrocarbon Research Inc | Verfahren zur kohlehydrierung bei erhoehten temperaturen |
EP0341554A1 (de) | 1988-05-03 | 1989-11-15 | BASF Corporation | Elektrisch leitfähige textile Fäden |
DE3921249A1 (de) | 1988-07-08 | 1990-01-11 | Sandoz Ag | Ir-absorbierende textilien |
FR2799392A1 (fr) | 1999-10-06 | 2001-04-13 | Tedeco | Nouveau procede de preparation de dispersions stables de nanoparticules d'oxydes metalliques, et de fabrications de fibres revetues par ces oxydes, et fibres et articles ainsi obtenus |
US20030113498A1 (en) * | 2000-06-27 | 2003-06-19 | Tatsuya Zenda | Moisture-permeable, waterproof and heat insulating fabric and moisture-permeable, waterproof and heat insulating resin film with releasing paper |
RU2196855C1 (ru) | 2001-07-12 | 2003-01-20 | Институт химии растворов РАН | Состав пасты для печати целлюлозосодержащих материалов кубовыми красителями |
JP3853185B2 (ja) * | 2001-09-26 | 2006-12-06 | 帝人ファイバー株式会社 | 保温性布帛 |
DE10240802A1 (de) | 2002-08-30 | 2004-04-15 | W.L. Gore & Associates Gmbh | IR reflektierendes Material |
JP4007497B2 (ja) | 2002-10-28 | 2007-11-14 | グンゼ株式会社 | 光発熱性肌着 |
DE10258014A1 (de) | 2002-12-12 | 2004-06-24 | Texplorer Gmbh | Wärmetarnplane |
JP2005212471A (ja) | 2004-01-31 | 2005-08-11 | Sozai Kk Nippon | 省エネ保温カバー |
JP2005290585A (ja) | 2004-03-31 | 2005-10-20 | Taiwan Textile Research Inst | 温度制御繊維製品及びその製造方法 |
JP4355945B2 (ja) | 2004-11-08 | 2009-11-04 | 住友金属鉱山株式会社 | 近赤外線吸収繊維およびこれを用いた繊維製品 |
KR101525618B1 (ko) * | 2005-05-25 | 2015-06-04 | 고어 엔터프라이즈 홀딩즈, 인코포레이티드 | 적외선 차단 재료 |
PT103361A (pt) | 2005-09-30 | 2007-03-30 | Sasaki Internacional Ind E Com | Processo de fabrico de edredão |
JP2009062652A (ja) | 2007-09-07 | 2009-03-26 | Asakura Senpu Kk | 赤外線吸収能繊維及び赤外線吸収能付与染色方法 |
JP5230464B2 (ja) | 2008-01-30 | 2013-07-10 | 小松精練株式会社 | 赤外線吸収布帛およびその製造方法 |
PT2262945E (pt) | 2008-03-28 | 2013-04-30 | Clariant Finance Bvi Ltd | Influenciando a reflectância no infravermelho próximo de materiais têxteis tingidos |
DE102009006832A1 (de) * | 2009-01-30 | 2010-08-05 | Bayerisches Zentrum für Angewandte Energieforschung e.V. | Flüssige oder halbfeste Formulierung spektralselektiver Partikel zur Beschichtung flexibler Körper sowie Verwendung dieser |
WO2010120531A2 (en) | 2009-04-01 | 2010-10-21 | Cornell University | Conformal particle coatings on fiber materials for use in spectroscopic methods for detecting targets of interest and methods based thereon |
TWI396788B (zh) | 2009-10-01 | 2013-05-21 | Taiwan Textile Res Inst | 彩色織物 |
-
2012
- 2012-06-06 DE DE102012209598A patent/DE102012209598A1/de not_active Withdrawn
-
2013
- 2013-06-04 WO PCT/EP2013/061500 patent/WO2013182568A2/de active Application Filing
- 2013-06-04 EP EP13729627.3A patent/EP2859145B1/de active Active
Non-Patent Citations (1)
Title |
---|
See references of WO2013182568A2 * |
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WO2013182568A2 (de) | 2013-12-12 |
WO2013182568A3 (de) | 2014-01-30 |
EP2859145B1 (de) | 2017-03-15 |
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